Open access

The Effects of Some Neuropeptides on Motor Activity of Smooth Muscle Organs in Abdominal and Pelvic Cavities

Written By

Anna Tolekova, Petya Hadzhibozheva, Tsvetelin Georgiev, Stanislava Mihailova, Galina Ilieva, Maya Gulubova, Eleonora Leventieva-Necheva, Kiril Milenov and Reni Kalfin

Published: 19 September 2012

DOI: 10.5772/48417

From the Edited Volume

Neuroendocrinology and Behavior

Edited by Tomiki Sumiyoshi

Chapter metrics overview

2,393 Chapter Downloads

View Full Metrics

1. Introduction

1.1. Neuropeptides

Neuropeptides are intracellular peptides, composed of short chains of amino acids and found in brain tissue. They are often localized in axon terminals at synapses and are released as intercellular messengers that transmit information in the central nervous system, gastro-intestinal tract etc. Many are also hormones released by nonneuronal cells. Neuropeptides can be divided and grouped according their site of synthesis and secretion or their structural or functional characteristics. Currently recognized neuropeptides include all hypothalamic releasing hormones, pituitary hormones, gastro-intestinal and brain peptides, some circulating hormones, opioide peptides, neurohypophyseal hormones etc (Siegel, 2006). Some neuropeptides are secreted by the nerve terminals with conventional neurotransmitters. But which are the differences between the classical neurotransmitters and the neuropeptides? The precursors of neuropeptides have at least 90 amino acids residues - larger than the precursors of the neurotransmitters. The synthesis of neuropeptides is carried in the neuronal soma and then is transported to the axonal ends. The secretion of neuropeptides requires lower concentration of intracellular Ca2+ in comparison to transmitters. After secretion the neuropeptides or their precursors are reused in the synapse. The concentration of the neuropeptides in the tissue is very low and they interact with the receptors at lower concentrations than neurotransmitters. Neuropeptides appearance and secretion are very plastic (Siegel, 2006). For example in pathological conditions, the number of endocrine cells that secrete neuropeptides can not only increase but also appear unusual locations as a result of additional stimulation (Gulubova et al., 2012).

1.2. Vasopressin

Vasopressin (arginine vasopressin, AVP) is the first identified neuropeptide. AVP is a nonapeptide that is synthesized in magnocellular and parvocellular neurons, located in the paraventricular and supraoptic nuclei of the hypothalamus (Swaab et al., 1975). Most of vasopressin is released from the axonal terminals of magnocellular neurons directly iinto the bloodstream of the posterior pituitary.

The effects of AVP are mediated mainly via V1and V2 receptors.

V1 receptors are located on the vascular smooth muscle membranes. They are also found in myometrium and urinary bladder smooth muscle cell membranes. V1-receptor activation mediates vasoconstriction by receptor-coupled activation of phospholipase C and release of Ca2+ from intracellular stores via the phosphoinositide cascade (Thibonnier, 1992, Briley et al., 1994).

V2 renal receptors are present in the renal collecting duct system and endothelial cells. Kidney V2 receptors interact (by the G protein complex) with adenylyl cyclase to increase intracellular cyclic adenosine monophosphate (cAMP) and cause retention of water (Orloff & Handler, 1967).

V3 pituitary receptors (formerly known as V1b or AVPr1B), have central neural system effects, such as increasing adrenocorticotropic hormone production, activating different G proteins, and act via increasing intracellular cAMP (Thibonnier et al, 1997, Holmes et al, 2001, Kam et al, 2007).

The classical effects of vasopressin are mainly related to maintenance of water-electrolyte homeostasis and blood pressure. During the last years the data about the effects of this neuropeptide on brain function and behavioral reactions increase. The brain effects of vasopressin can be divided into two main types: those related to its peripheral effects such as hormone and focused on the maintenance of water balance. Others are associated with higher brain functions as learning, memory, emotion and they are independent of its hormonal effects (Frank & Landgraf, 2008). Vasopressinergic axons propelled from hypothalamus to many brain regions as hipocampus, septum, amygdala and brainstem, secrete AVP that acts as neurotransmitter. This extrahypothalamic vasopressin network is an anatomical basis of involvement of limbic-midbrain structure in processes of learning and memory. AVP facilitates consolidation and retrieval of memory (Kovacs et al., 1979)

Vasopressin participates in formation of circadian rhythms and regulation of biological clock. The suprachiasmatic nucleus (SCN) is responsible for generation of circadian rhythmicity in mammalian brain and is an obvious source for a vasopressin innervation of GABAergic neurons located in this area (Hermes et al., 2000). A significant diurnal variation in vasopressin release in the SCN was detected, with the highest levels occurring during midday and a trough around midnight (Kalsbeek et al., 1995). It was demonstrated that melatonin synthesis was stimulated after local injection in pineal gland of vasopressin. Also the night melatonin plasma concentration was increased after prolonged period of water deprivation. These results show that vasopressin can modulate melatonin synthesis in the rat pineal (Barassin et al., 2000). The suprachyasmatic nuclei, that are the main biological clock, contain vasopressinergic neurons. They demonstrate noticeable daily variation activity. In animals these vasopressin secreting neurons have very important role in the control of day/night rhythms. The reduced secretion of vasopressin in suprachyasmatic nuclei could contribute to the violation of sleep-wake rhythms during ageing and to development of depression (Kalsbeek et al., 2010).

Vasopressin takes part in the regulation of maletypical social behaviors, vocal communication, aggression, and paternal care (Goodson & Bass, 2001). There are established projections of vasopressinergic neurons from the cells of the bed nucleus of the stria terminalis to the lateral septum with higher levels of density in nonaggressive animals. These lacalizations demonstrate the significance of vasopressinergic brain network in development of aggression (Compaan, 1993).

AVP is a potent regulator of complex social maternal behaviors. The maternal cares that are vasopressin dependent were found to be independent of dam’s trait anxiety. The authors suggest that manipulation of AVP system could contribute to the treatment of mothers suffering from postpartum depression (Bosch & Neumann, 2008).

Vasopressin, secreted in olfactory bulb is involved in the processing of stimuli that are important for social behaviors. In this anatomic region Tobin and coauthors (2010) have identified population of vasopressin neurons, most of which do not project outside the olfactory bulb. They discuss the importance of vasopressin secreting neurons in filtering out of the olfactory signals and in social recognition (Tobin et al., 2010).

Vasopressin and corticoliberin, secreted from parvocellular portion of paraventricular nucleus in stress condition synergistically activate ACTH-adrenal axis. Aguilera supposed that in chronic stress there is preferential activation of vasopressin rather than corticoliberin and as a consequence a feedback mechanism is disintegrated (Aguilera, 1994). In contrast Zelena et al. (2006) demonstrate that AVP does not play critical role in stimulation of hypothalamic-pituitary axis during chronic stress, but its role in acute stress is more important.

1.3. Ghrelin

Ghrelin is a multifunctional peptide hormone (28 amino acids) secreted from the cells of the diffuse neuro-endocrine system. Ghrelin-secreting cells are found from the stomach to the colon (in the oxyntic glands of the fundus and less in the small and large intestine) (Broglio et al., 2002; Lee et al., 2002; Inui et al., 2004). Ghrelin has been detected in the central nervous system, e.g. in arcuate nucleus and hypothalamus (Lu et al., 2002), in pancreas (Date et al. 2002), in some cells of the immune system (lymphocytes and monocytes) (Mager et al., 2008) and also in human ovaries and testes (García et al., 2007). There is a hypothesis that ghrelin might have not only endocrine but also autocrine and paracrine mechanism of action.

The presence of ghrelin receptor subtype GHS-R1a is detected in hypothalamus (n.arcuatus) and the pituitary gland, in multiple organs with nonendocrine and endocrine function (heart, lung, liver, kidney, pancreas, stomach, small and large intestines, adipose tissue, immune cells, gonads, thyroid gland, adrenal gland) (Broglio et al., 2003; Inui et al., 2004; Van Der Lely et al., 2004) and in gastrointestinal vasculature (Mladenov et al., 2006). They are also expressed by lumbosacral autonomic preganglionic neurons of the micturition reflex pathways (Ferens et al., 2010)

The activation of the receptor causes the stimulation of the G-protein subunit Gα11. This leads to the activation of intracellular signaling cascades via the phospholipase C (PLC) (Vartiainen, 2009).

The principal physiological action of ghrelin is the stimulation of secretion of growth hormone. Therefore ghrelin is a hormone with anabolic effect. It participates in the regulation of metabolism, energy homeostasis and feeding behaviors which are mediated via a complex neuroendocrine network (Van Der Lely et al., 2004). Ghrelin increases appetite and food intake and decreases fat utilisation as a metabolic fuel and increases fat storage in the adipose tissue. Ghrelin modulates gastic motility and emptying and gastric acid secretion and stimulates ileum peristalsis, most of these effects being vagally mediated (Ghigo et al., 2005). It induces fasted motor activity in the duodenum (Fujino et al., 2003). Ghrelin activity is mediated via enteric nervous system (Tack et al., 2006).

Ghrelin and its receptors are present not only in the peripheral tissues but also in the central nervous system (Kang et al., 2011). Ghrelin functions as a peripheral hormone that is released mainly from the stomach and affects the hypothalamus, but also as a neuropeptide in hypothalamus (Kojima and Kangawa, 2005). Like other neuropeptides, Ghrelin is widely distributed in the brain in key areas of emotional regulation, and plays role as modulators of behavioural states (Kang et al., 2011). Ghrelin plays an important role in the regulation of energy balance by regulating food intake, body weight, glucose homeostasis and feeding behaviour which are mediated by a complex neuroendocrine network (Kalra et al., 1999; Van Der Lely et al., 2004). The regulation of energy balance is related to somatic growth and instinctive behaviour, including feeding, reproduction and emotion, and is a complex phenomenon involving interaction of the central and peripheral nervous systems, neuroendocrine system and gastrointestinal system (Matsuda et al., 2011). Ghrelin induces in the brain an orexigenic effect, modifies locomotor activity and also is involved in the control of psychophysiological functions and regulation of metabolism (Kang et al., 2011). The hypothalamic region of the brain plays very important role in the regulation of feeding and neuroendocrine functions (Kalra et al., 1999). Many types of neurons in the hypothalamus and related regions express ghrelin and some neuropeptides, such as, orexin, NPY, agouti-related peptide (AGRP), melanin-concentrating hormone (MCH) and other, which are implicated in the regulation of feeding behaviour and also in energy homeostasis in mammals (Eva et al., 2006; Kalra et al., 1999; Pickar et al., 1993). Ghrelin increases orexigenic effect and food intake but decreases energy expenditure thus inducing weight gain. (Kojima & Kangawa, 2005; Van Der Lely et al., 2004). Ghrelin exerts its central orexigenic effect through activation of hypothalamic neurons in the arcuate nucleus, important area involved in the regulation of energy balance and in addition it stimulates the neurons of other areas of the central nervous system, for example nucleus paraventricularis, dorsomedial parts of hypothalamus, and areas in the brain stem nucleus tractus solitarius and the area postrema, which all take part in the modulation of appetite control (Lim et al., 2010; Vartiainen, 2009). Ghrelin-secreting hypothalamic neurons send efferent fibers onto key circuits involved in the central regulation of energy homeostasis. They balance the activity of orexigenic neuropeptide Y/agouti-related peptide neurons in the arcuate nucleus and the activity of anorexigenic pro-opiomelanocortin (POMC) neurons that secrete alpha melanocyte stimulating hormone (α-MSH) and thus modulate the resultant effect (Van Der Lely et al., 2004).

Several new intracellular targets/mediators of the appetite-inducing effect of ghrelin in the hypothalamus have recently been identified, including the AMP-activated protein kinase, its upstream kinase calmodulin kinase kinase 2, components of the fatty acid pathway and the uncoupling protein 2 (Lim et al., 2010).

Recently, it has been demonstrated that ghrelin plays an important role in the regulation of central and peripheral lipid metabolism through specific control of hypothalamic AMP-activated protein kinase (AMPK), a critical metabolic regulator of both cellular and whole-body energy homeostasis (Kola et al., 2005).

Centrally administered ghrelin has various effects such as arousal, increasing gastric acid secretion and gastrointestinal motility, inhibition of water intake and release of some hormones from the pituitary, mainly growth hormone (Hashimoto et al., 2011).

Ghrelin may be synthesized in the hypothalamus. Ghrelin have hypothalamic actions on growth hormone-releasing hormone neurons (Sun et al., 2007). Ghrelin acts centrally to exert a global stimulatory effect on the hypothalamo-pituitary-adrenal axis. Ghrelin increases absolute whole adrenal gland weight and whole adrenal gland volume and elevates blood concentrations of ACTH, aldosterone and corticosterone (Milosević VLj et al., 2010). Ghrelin may function as a metabolic modulator of the gonadotropic axis, with inhibitory effects in line with its role as signal of energy deficit. These effects likely include inhibition of luteinizing hormone secretion, as well as partial suppression of normal puberty onset (Tena-Sempere, 2008).

Ghrelin-immunoreactive neurons are present in the paraventricular, dorsomedial, ventromedial and arcuate nuclei, areas important for circadian output. Contrary to the effects of ghrelin on appetite, growth hormone release and the sleep–wake cycle, little is known about the effects of ghrelin on circadian rhythms (Yannielli et al., 2007).

Central ghrelin is also a gastroprotective factor in gastric mucosa. The gastric protection elicited by central ghrelin requires integrity of capsaicin-sensitive sensory neurons, which play an important role in gastric cytoprotection. Growing evidence indicates that the mechanisms triggered by peptides to increase resistance of the gastric mucosa involve changes in the release of gastric protective factors. Endogenous prostaglandins are involved in ghrelin gastroprotection (Sibilia et al., 2008).

The short-term activation of AMPK in turn results in decreased hypothalamic levels of malonyl-CoA and increased carnitine palmitoyltransferase 1 (CPT1) activity. Ghrelin deficiency induces reductions in both de novo lipogenesis and beta-oxidation pathways in the hypothalamus. There are reductions in fatty acid synthase (FAS) mRNA expression both in the ventromedial nucleus of the hypothalamus and whole hypothalamus, as well as in FAS protein and activity. CPT1 activity is also reduced. Chronic ghrelin treatment does not promote AMPK-induced changes in the overall fluxes of hypothalamic fatty acid metabolism in normal rats and this effect is independent of ghrelin status. In addition, ghrelin plays a dual time-dependent role in modulating hypothalamic lipid metabolism. (Diéguez C et al., 2010; Sangiao-Alvarellos et al., 2010)

A reciprocal relationship exists between ghrelin and insulin, suggesting that ghrelin regulates glucose homeostasis (Sun et al., 2007).

1.4. Angiotensin II

The octapeptide Angiotensin II (Ang II) is the main effector of the renin-angiotensin system (RAS). Ang II is generated in circulation or locally in tissues in the kidney, blood vessels, heart, and brain and etc.

The signal transduction mechanism for AT1 receptors is well known. AT1 receptors are distributed in adult tissues including blood vessel, heart, kidney, adrenal gland, liver, brain, and lung. These receptors activate phospholipase A2, phospholipase C, phospholipase D and L-type Ca2+ channels and inhibiting the adenylyl cyclase (Shokei & Hiroshi, 2011).

AT2 receptors are ubiquitously expressed in developing fetal tissues, suggesting a possible role of these receptors in fetal development and organ morphogenesis. AT2 receptors expression rapidly decreases after birth, and in the adult. Expression of these receptors are limited mainly to the uterus, ovary, certain brain nuclei, heart, and adrenal medulla. In various cell lines, AT2 receptors activated protein tyrosine phosphatase was shown to inhibit cell growth or induce programmed cell death (apoptosis) (Kim and Awao, 2011).

Ang II has a multifunctional role. It is general regulator of salt and water metabolism, thirst, sympathetic outflow and vascular smooth muscle cell tone. As a result Ang II acts as a principal controller of long term regulation of blood pressure (Robertson, 2005; Watanabe et al., 2005). Later, Ang II was found to exert long-term effects on tissue structure, including cardiac hypertrophy, vascular remodeling, and renal fibrosis (Watanabe et al., 2005).

The key effector of peripheral renin-angiotensin system (RAS) - Ang II in circulation does not cross blood-brain barrier. Therefore it interacts on brain regions that lack the blood-brain barrier as circumventricular areas, organum vasculosum laminae terminalis, where Ang II stimulates salt appetite, thirst and vasopressin secretion (Fitts et al., 2000). Also, it influences neuronal activity in area postrema and takes part in central regulation of blood pressure (Otsuka et al., 1986).

Many immunohistochemical studies demonstrate the distribution of all components of RAS - angiotensinogen, Ang I, Ang II and renin in several brain regions of rats. Immunoreactivity for Ang II was detected in neurons and vessels in the brainstem, cerebellum, hypothalamus, basal ganglia, thalamus and cortex while for angiotensinogen and Ang I were found in neurons of the hypothalamic nuclei in rats (McKinley et al., 2003; Von Bohlen et al., 2006). AT1 receptor binding sites with higher density were localized in the lamina terminalis, hypothalamic paraventricular nucleus and the nucleus tractus solitaries, lamina terminalis and the subfornical organ. The median preoptic nucleus also contains membranes rich in AT1 receptors. All regions that are included in the regulation of cardiovascular functions as caudal ventrolateral medulla, and the midline raphe, also have AT1receptors (Allen et al., 1999; Lenkei et al., 1997). In the midbrain -in the lateral parabrachial nucleus, substantia nigra and periaqueductal gray AT1 receptors are presented from moderate to high densities (Lenkei et al., 1997). These localizations of RAS brain components show that Ang II is involved in the regulations of thirst, drinking, facilitating vasopressor effects and secretion of vasopressin, adrenocorticotrophic and luteinizing hormones. Ang II also stimulates secretion of neurotransmitters such as noradrenaline and 5-hydroxytryptamine (5-HT) and inhibits acetylcholine release. The brain RAS appears to be also an important modulator of the blood pressure circadian rhythm and it influences renal renin release.

Recent findings demonstrate that central effects of Ang II contribute to facilitated learning and enhance associative memory and learning possibly with differential effects on acquisition, storage and recall. Brain RAS is involved in the development of affective disorders and Ang II has a modulating effect of on anxiety (Georgiev & Yonkov, 1985).

RAS receptors alterations have been found in some neurodegenerative disorders - Parkinson‘s and Huntington’s disease (Ge & Barnes, 1996). The number of AT1 receptors in caudate nucleus, putamen and substantia nigra was significantly decreased in Parkinson’s disease patients in comparison to controls. In Huntington’s disease patients, AT1receptors was found to be slightly decreased in putamen (Ge & Barnes, 1996). AT2 receptors that are localized in caudate nucleus was decreased in Parkinson’s and increased in Huntington’s disease patients. The receptor alterations were considerable; therefore the authors have concluded that brain RAS seems to decisively contribute to the pathology of the dopaminergic nigrostriatal pathway in these patients and may be a novel therapeutic target for neurodegenerative disorders (Savaskan, 2005).

1.5. Cholecystokinin

In 1928 Ivy and Oldberg extracted from dog duodenal mucosis a substance which injected intravenously contracted the gallbladder. The authors named this substance cholecystokinin (CCK). Later, Harper & Raper (1943) found a compound in this extract that stimulated the pancreatic secretion and called it pancreozymin. Purifying both hormones and determing their amino-acid sequention, Mutt (1980) proved them to be the same linear polypeptide, containing 33 amino-acid residues, and proposed the hybrid name “cholecystokinin-pancreozymin”. Different CCK forms have been shown to exist: CCK-58, CCK-39, CCK-33, CCK-27, CCK-12, CCK-8, CCK-4, all of them containing a bioactive C-terminal. CCK-58 and CCK-39 are precursors of CCK-33 and by the degradation of the latter the shorter forms are obtained. Cholecystokinin octapeptide (CCK-8) is the most active one and is most widely spread in the gastro-intestinal tract and in the central nervous system. A cholecystokinin analogue, named caerulein, has been isolated from the skin of the frog Hyla caerulea.

CCK and gastrin possess identical 5 aminoacids at their C-terminals that are the biologically active part of both hormones. The dissimilarities in their potency and physiological activity are determined by the different positions of the Tyr-residue in the molecules of both peptides. When the Tyr-residue is in the 6th position, the peptide (gastrin) strongly potentiates the gastric secretion, its stimulating effect on the gallbladder contractions and pancreating secretion being much weaker. With the Tyr-residue in the 7th position, CCK markedly enhances the gallbladder motility and the pancreatic secretion.

Immunohistochemical studies have shown that CCK is synthesized in the mucosal endocrine cells type I and type K of the small intestine, and in the endocrine cells type A of the pancreas. CCK-immunoreactivity has been also identified in the vagus nerve. Cholecystokinin is so called “brain-gut” neuropeptide – it is also produced by enteric neurons, and is widely and abundantly distributed in the brain.

The food intake in the small intestine is the main physiological stimulus for the CCK release – masts, proteins and aminoacids are the most powerful stimulants among the foods. The plasma CCK concentration increases from 1-2 pmol/l to 6-8 pmol/l after feeding (Cantor, 1986). Cholecystokinin plays a key role in facilitating digestion within the small intestine – this peptide stimulates delivery into the small intestine of digestive enzymes from the pancreas and bile from the gallbladder. Recently it was shown that CCK-8 can reduce food intake by capsaicin-insensitive, nonvagal mechanisms (Zhang & Ritter, 2012).

Mechanisms of secretion of cholecystokinin group peptides into the gastro-intestinal tract are as follows: a) Endocrine mechanism – the peptide is released by the endocrine cell in a blood vessel and is afterwards transported by the circulation to the effector cell; b) Paracrine mechanism – the peptide is released by the endocrine cell in the intracellular space, reaching afterwards the effector cell by diffusion; c) Neurotransmitter mechanism – the peptide is released by the nerve terminal in the synaptic cleft and affects afterwards the activity of the effector neuron; d) Neuroendocrine mechanism – the peptide is released by the neuron in a blood vessel.

The peptide hormone CCK realizes its effects via binding to specific receptors localized on the cell membranes of the target organs. Two types of cholecystokinin receptors have been characterized so far: CCKA and CCKB which are approximately 50 % homologous (Dufresne et al., 2006).

CCKA (gastro-intestinal) receptors. They prevail in the peripheral target organs (pancreas, gallbladder, small intestine), as well as in the vagus nerve afferent fibres, mediating the pancreatic enzyme secretion and the gallbladder and ileum motility (Crawley & Corwin, 1994; Xu et al., 2008). CCKA-receptors have also been identified in some brain regions where they take part in the modulation of dopaminergic neurotransmission, and in the regulation of food behavior - satiety effect (Lieverse et al., 1995).

CCKB (brain) receptors. They have been identified in various brain structures, as their number is largest in the cortex, hippocampus and limbic structures (Hokfelt et al., 1985). CCKB receptors, similar or identical to the peripheral gastrin receptors, have been demonstrated in peripheral organs, too.

Cholecystokinin is a major peptide hormone in the gut and a major peptide transmitter in the brain. Its synthesis requires endoproteolytic cleavage of proCCK at several mono- and dibasic sites by prohormone convertases. On one hand cholecystokinin is a classical gut hormone and a growth factor for the pancreas. On the other, the CCK gene is expressed also in large quantities in cerebral and peripheral neurons from where CCK peptides are released as potent neurotransmitters and modulators. Accordingly, cerebral CCK defects have been associated with major neuropsychiatric diseases such as anxiety, schizophrenia and satiety disorders (Crawley & Corwin, 1994; Liddle, 1997).

CCK is also a key component of the aggression facilitating circuitry in the brain (Luo et al., 1998), and it is released during inter-male fighting (Becker et al., 2001). In addition to its many aversive motivational/emotional effects, CCK also plays a role in more positively valenced motivational states, such as mating (Dornan & Malsbury, 1989; Markowski & Hull, 1995), drug addiction (Crespi, 2000) and brain reward processes (Degen et al., 2001, Josselyn, 1996).

It was demonstrated that CCK is colocalized with dopamine in ventral striatal dopamine neurons (Hokfelt et al., 1980). Consistent with the neuronal colocalization and extensive overlap of expression between CCK and the dopaminergic system, CCK peptides have significant effects on dopamine mediated behaviors. Administration of CCK peptides exhibit many of the behavioral characteristics of antipsychotics including inhibition of conditioned avoidance responding (Cohen et al., 1982), inhibition of apomorphine-induced stereotypic behavior (Zetler, 1983), and inhibitionof amphetamine-induced hyperlocomotion (Schneider et al., 1983). Microinjection of CCK into the anterior nucleus accumbens inhibits dopamine release, inhibits dopamine-mediated behaviors and is blocked by a CCKA antagonist whereas injection into the posterior nucleus accumbens has the opposite effects and these effects are mediated by CCKB receptors (Vaccarino & Rankin, 1989, Crawley, 1992). Thus, it appears that different CCK-based circuitries in the brain can facilitate both negative and positive emotional processes. It is also interesting to note that selective CCKB agonists that cross the blood brain barrier such as pentagastrin and CCK-4 are used to induce panic attacks in clinical studies. Consequently, a CCK agonist for schizophrenia would need to be either nonselective or CCKA selective.

CCK was the first gut hormone discovered to have anoretic effects. Its actions include inhibition of food intake, delayed gastric emptying, stimulation of pancreatic enzyme secretion, and stimulation of gall bladder contraction. These effects are mediated via binding to CCK receptors on the vagus nerve. CCK administration to humans and animals inhibits food intake by reducing meal size and duration. However, at high dose nausea and taste aversion have been detected making CCK an unlikely candidate for an anti-obesity treatment.


2. Materials and methods

Wistar rats of both sexes weighting 200–250 g were used. The experiment was carried out in accordance with the national regulations and DIRECTIVE 2010/63/EU of the European Parliament and of the Council of 22 September 2010 concerning the protection of animals used for scientific and experimental purposes. The animals were anesthetized with Nembutal 50 mg/kg intraperitoneally and exsanguinated. Abdominal cavity was opened and longitudinal strips from different parts of gastro-intestinal tract, urinary bladder and uterus horn were dissected out. The isolated organs were transferred immediately in cold Krebs solution 3 °C), containing following composition in mM): NaCl—118.0, KCl—4.74, NaHCO3—25.0, MgSO4—1.2, CaCl2—2.0, KH2PO4—1.2 and glucose 11.0.

Longitudinal strips approximately 2 mm wide, 0.5 mm thick and 8 mm long) were dissected following the direction of the muscle bundles. The two ends of each strip were tied with silk ligatures. The distal end was connected to the organ holder; the proximal end was stretched and attached to a mechano-electrical transducer FSG-01 (Experimetria, Ltd., Hungary) via a hook. The preparations were mounted in organ baths TSZ-04/01, containing Krebs solution, pH 7.4, continuously bubbled with Carbogen (95% O2, 5% CO2). The organ baths were mounted in parallel above an enclosed water bath, maintaining the solution temperature at 37 °C. Each smooth muscle strip was initially stretched to a tension of 1.0 g followed by 90 minutes of equilibration. During this period, the smooth muscle strips were replenished with fresh Krebs solution at 15-th min, 60-th min and 75-th min.

After initial period of adaptation, they were treated with the solution of different neuropeptides, and the obtained responses were registered.

The phasic contractions of the smooth muscles before application of neuropeptide and the changes of motor activity, expressed as tonic contractions, relaxations or lack of reaction after treatment were recorded. The contractile activity signals were transduced by mechanical-force sensor, amplified, digitized and recorded using ISOSYS ADVANCED digital acquisition software, produced by Experimetria Ltd., Hungary.

Chemicals and drugs

Ang II (Sigma-Aldrich), vasopressin (Sigma-Aldrich), ghrelin (PolyPeptide Group) synthetic octapeptide of cholecystokinin (Squibb, USA), acetylcholine chloride (Sigma-Aldrich), hexamethonium chloride (Sigma-Aldrich) were solubilized in bidistillated water. All reagents for the preparation of Krebs solution were purchased from Sigma-Aldrich.

Data analysis and statistic processing

The recorded force-vs.-time curves permit determination of amplitudes and integrated force of contraction, the latter represented by the area under the curve (AUC), as well as defining of time parameters. Data acquisition and the initial conversion of the experimental data for the later analysis was performed with KORELIA – Processing software (Yankov, 2010). For later analysis, evaluation and identification was used KORELIA-Dynamics program. (Yankov, 2006; Yankov, 2011).

Following time parameters were examined Figure 1:

  • Thc (s) – first half contraction time - time interval between the start of the smooth muscle contraction (SMC) and half-contraction moment (Thc = t hc - t 0);

  • T(c-hc) (s) – second half contraction time - - time interval between the end of Thc and maximum peak of the SMC (T(c-hc) = tpeak-thc)

  • Tc (s) – contraction time - time interval between the start of the SMC and the moment of the maximum peak (Tc = t peak - t 0);

  • Thr (s) – half-relaxation time: time interval between the moment of the maximum peak tpeak and the moment when the curve decreases to Fmax/2 (Thr = thr - tpeak);

  • Tchr (s) – contraction plus half-relaxation time: time between the start of the SMC and t hr (Tchr = thr – t0).

Figure 1.

Smooth muscle contraction (SMC) - graph and parameters. Fmax – maximal force of the SMC; Fmax/2 – half of maximal force of the SMC; t0 – start of SMC. t 0 = 0; thc – half-contraction moment; tpeak – the moment of the maximum peak Fmax; thr – the moment when the curve decreases to Fmax/2.

The duration of the tonic contraction was defined from the beginning of the contraction, until the amplitude fell to 50%.

For a more correct and acurate comparison between the parts of the gastrointestinal tract was performed normalization of the different intervals as a relative part of total length of the process Txn=Tx/chr). As a result the following normalized parameters were obtained: Thcn, Tcn, T(c-hc)n, Thrn.

The gall bladder pressure in vivo was recorded in six conscious dogs weighing 18 to 20 kg. The animals were starved for 18 hours and were then anesthetized with chloralose (90 mg/kg i.v.). Laparotomy was performed through upper midline abdominal incision. Gall bladder bile was aspirated with a syringe. The bile volume was between 30 and 40 ml. A small balloon mounted on the top of a polyethylene catheter was introduced into the gall bladder. Experiments were started four weeks after surgery and were carried out twice a week at of at least two-day intervals. The dogs were deprived of food, but were given water ad libitum for 18 hours before each trial. The balloon was filled with 1 ml distilled water and connected through a catheter to a pressure transducer. The changes in gall bladder pressure were measured in mmHg. The first 40-min records were used as controls. Cholecystokinin octapeptide was then injected i.v. at increasing doses every 30 min. Atropine or hexamethonium was administered before cholecystokinin.

Obtained data were processed by the statistical program Statistica 6.1, StaSoft, Inc. and presented as mean ± standard error. A P-value less than or equal to 0.05 was considered to be statistically significant.


3. Results and discussions

3.1. Urinary bladder

The coordination of smooth muscle activity of the urinary tract in the process of the urine evacuation is regulated by complex, and not yet fully understood interactions between neural and hormonal control mechanisms (Dixon et al., 1997).

The urinary bladder is innervated by three groups of peripheral nerves: sacral parasympathetic (Helm et al., 1982; Crowe & Burnstock, 1989; Gabella & Uvelius, 1990; Lasanen et al., 1992; Uvelius & Gabella, 1998), thoracolumbar sympathetic (Downie, 1981; Feher & Vajda, 1981) and sacral sensory (De Groat & Booth, 1993). According to the secreted mediator in the neural terminals innervation is classified as cholinergic, adrenergic, and non-adrenergic, non-cholinergic (NANC) (Callahan & Creed, 1986). In humans detrusor neurotransmission is exclusively cholinergic (Andersson et al., 1982; Sibley, 1984; Chen et al., 1994), while its adrenergic innervation is sparse, nonuniform, and it is considered non-essential for micturition function (de Groat & Booth, 1984; Janig & McLachlan, 1987).

A lot of different neuropeptides have been found to be synthesized, stored and released from organs in the lower urinary tract (LUT). Some of them are secreted from the peripheral neural terminals of the autonomic nervous system – vasoactive intestinal peptide (VIP), tachykinins (substance P), neuropeptide Y, calcitonin gene-related peptide, neurokinin A. Others which act by para- and autocrine mechanisms as angiotensin II are locally synthesized. The exact function of many of these peptides has not been fully established, however they may play role in a sensory and efferent innervation (de Groat & Kawatani, 1985; Burnstock, 1990; Maggi, 1991) or serve as neuromodulators in the ganglia or at the neuromuscular junctions. Their actions have been thought to include mediation of the micturition reflex activation, smooth muscle contraction, potentiation of efferent neurotransmission and changes in vascular tone and permeability (Maggi, 1991, 1995; Hernandez et al., 2006).

A few hormones with systemic circulation – vasopressin, oxytocin, are influencing bladder function (Uvelius B. et al., 1990; Romine & Anderson, 1985). These also include a newly discovered peptide ghrelin, which is secreted from the gastrointestinal tract, and stimulates contractions of smooth muscles of blood vessels and gastro-intestinal tract (Tack et al., 2006; Wiley & Davenport, 2002)

Angiotensin II and urinary bladder

There is insufficient information on the effect of Ang II on non-cardiovascular organ smooth muscles (Touyz & Berry, 2002). The interactions of the Ang II with the urinary bladder are of particular interest regarding the genesis and treatment of the disorders of the micturition. The physiological effects of Ang II on the function of the urinary bladder and the transduction mechanisms which mediate it have not been fully elucidated. Ang II and its precursor Ang I cause dose-dependent contractions of muscle strips from rat urinary bladder (Andersson et al., 1992). According to experimental data of Anderson and co-authors Ang II acts as a modulator in neurotransmission in the urinary bladder (Andersson & Arner, 2004). There are research data confirming that Ang II carries out its physiological effects by binding to membrane AT1 receptors (Tanabe et al.,1993), whose number on the surface of detrusor smooth muscle cells is regulated by the dietary content of sodium and potassium and the age of experimental animals (Weaver-Osterholtz et al., 1996; Szigeti et al., 2005). AT1 receptors activate PLC, dihydropyridine-sensitive Ca2+-channels and inhibit adenylilcyclase, thus reducing intracellular cAMP concentration (Chiu et al., 1994).

Our experiments show that the administration of Ang II solution to the smooth muscle stirps induce tonic contractions, in confirmation of the findings from other researchers concerning its effect on urinary bladder contractile activity. The increased amplitude of contraction following the administration of Ang II in the presence of increased extracellular Ca2+ provided evidence of additive synergism (Hadzhibozheva et al., 2009; Tolekova et al., 2010). The blockade of AngII-induced tonic contraction after the administration of blockers of T-type Ca2+ -channels unequivocally showed the role of transmembrane Ca2+ -influx in the initiation of smooth muscle contraction (Ilieva et al., 2008). The Ang II bindings to its membrane receptors, leads to activation of phospholipase C, which results in formation of inositol triphosphate, which triggers release of Ca2+ from sarcoplasmatic reticulum (SR). It's also well known that Ang II causes calcium-induced calcium release in smooth-muscle cells. Angiotensin II causes depolarization and opening of VDCC, providing additional Ca2+ influx from the extracellular fluid (Seki et al., 1999). When moving inside the cell, Ca2+ binds to ryanodine receptors and triggers supplementary Ca2+ release from SR stores (Berridge, 2008). In the experiment we applied specific inhibitor to this particular calcium-induced Ca2+ release mechanism. The resulting lack of tonic contraction suggested that this signaling pathway, leading to intracellular calcium increase is of greater importance for the development of detrusor muscle contraction than the inositol triphosphate pathway. Our experimental data also showed that the increase of calcium in extracellular fluid produced additive synergistic effect on Ang II-mediated contraction of detrusor smooth muscle strips.

The circulating AngII is formed in blood under influence of angiotensin–converting enzyme (ACE). During the last decade a lot of new facts that significantly broaden our knowledge of the RAS have been accumulated. Local tissue RAS was found in the blood vessels, heart, kidneys, small intestines, pancreatic tissue, liver, ovaries and brain (Paul at al., 2006). Other enzymes involved in RAS and physiologicaly active metabolites of Ang I and Ang II were also found (Waldeck et al., 1997; Miyazaki & Takai, 2006).

A lot of recent studies have shown that Ang II acts as a cytokine and growth-like factor. (Kim & Iwao, 2000; Touyz & Berry, 2002). It regulates the smooth muscle mass in the bladder wall in normal and pathological conditions. Chronic bladder outlet obstruction causes changes in smooth muscle mass and connective tissue both in humans’ disease and under experimental conditions in rats (Yamada et al., 2009). The application of ACE blocking substances significantly reduce the quantity of the newly synthesized collagen in the bladder, which is an indirect indicator of the effects of the local RAS on developing pathologic hypertrophic changes in the bladder. Phull and coauthors (2007) showed that applying angiotensin receptor anatagonists, reduced urethral resistance on rat models with stress urinary incontinence.

The all main components of RAS – Ang I, Ang II and ACE are found inside bladder tissues (Weaver-Osterholtz et al., 1996). Tissue levels of Ang I and Ang II were higher than circulating levels, which confirms the existence of local synthesis in the urinary bladder, despite the lower measured activity of the angiotensin-converting enzyme, insitu is relatively This fact supports the hypothesis of auto- and paracrine actions of Ang II. It has been shown that Ang I also causes contraction of smooth muscle cells of the bladder, through the interaction with AT1 receptors.

Ang II -mediated contraction is not completely blocked after administration of ACE inhibitor (Lindberg et al., 1994). These facts indicate the existence of alternative pathways for the synthesis of Ang II. Urata and co-authors show that in the heart of the main enzyme converting Ang I to Ang II is a serine protease human himase (Urata et al., 1990). Andersson and co-authors found that application of enalaprilat not fully block contraction of urinary bladder detrusor stripts induced by Ang I (Andersson et al., 1992). This means that the remaining contractile effect is due to separate mechanism of Ang II formation.


Besides its vasoconstrictor activity, AVP is involved in the modulation of the intrinsic smooth muscle activity of the urinary system. Vargiu and coauthors demonstrate that AVP increases the contractile activity of upper urinary tract that is most pronounced in small calices, which are the main pacemaker of the urinary tract and is mediated by V1 receptors (Vargiu et al., 2004). It remains unaffected by the blockade of sodium channels with tetrodotoxin. However, the application of nifedipine and L-type calcium channels blockers reduced spontaneous and AVP-induced activity of smooth muscles of the upper urinary tract (Vargiu et al., 2004). This demonstrates the importance of transmembrane calcium influx for the contractile activity of smooth muscle of the lower urinary tract.

There is a data that shows the presence of V1-receptors in smooth muscle of the urinary bladder, who’s binding to AVP leads to activation of the inositol-triphosphate (IP3) pathway, similarly to binding to Ang II (Crankshaw, 1989; Dehpour et al., 1997). It was found that the removal of extracellular calcium prevents the effects of AVP, suggesting it possible involvement in the activation process (Crankshaw, 1989). In our experiments AVP application to the bladder detrusor smooth muscle strips stimulates powerful tonic contractions. This result supports currently available information on this issue (Uvelius et al., 1990).

Comparison of the effects of Ang II and AVP on contractile activity

Ang II and AVP, accomplish their effects through the formation of the second messenger IP3. The comparison of the independent effects of Ang II and AVP on urinary bladder strips shows contractions with approximately equal amplitude, but with integrated muscle force significantly increased after the application of AVP (Figure 2, Table 1) (Tolekova et al., 2010).

Fmax.g)AUCgs)Thc s)Tc-hc)Tc s)Thr s)Tchrs)
Ang II1,73±0,26115,13±20,712,6±1,619,7±532,3±3,361,5±13,693,7±13,3

Table 1.

Force and time-parametes means±SE) of Ang II- and AVP-induced contractions.

Figure 2.

Angiotensin II- and AVP – induced contractions after processing of signals with specialized software.

For detailed study and comparison of the tonic contractions under the influence of the two peptides, we are using time parameters, described in Yankov (2011) (Figure 1, Table 1), generated after signal processing with specialized software (Yankov, 2010). The similar parameters were used for investigation of the contractions of the skeletal muscles (Raikova & Aladjov, 2004). Our research results show that Ang II causes contractions with a shorter duration (shorter time for reaching Fmax/2 and Fmax). The AVP-induced response reaches significant AUC value at the expense of the lower rate of increased and decreased contractile activity (longer duration of Thr and Tchr). The greater length of AVP contraction time is mainly due to longer T(c-hc) period. It is particularly interesting that despite acting through the same transduction pathways, Ang II and AVP cause tonic contractions with different measured force. We assume that this difference, especially the higher speed of relaxation, might be related to the specific Ang II metabolism in bladder cells. Production of Ang III and Ang 1-7 may be a cause of the faster rate of relaxation (Varagic et al., 2008). The interactions of the two peptides – Ang II and AVP with the ion channels of the smooth muscle membrane may contribute additionally to the differences in the computed parameters and shape of the contraction graphic. There are existing data about the effect of AVP on the potassium channels of brain cells after fluid percussion brain injury indicating that AVP inhibited activity of the KATP and KCa channels (Armstead, 2001). It is known that the urinary bladder smooth muscle cells have a number of potassium channels, including ATP-dependent K channels and Ca2+-dependent K channels (Petkov et al., 2001). Interaction with those channels could be a possible explanation for the prolonged duration of AVP action on smooth muscle contractions.

On the other hand, Ang II stimulates the activity of L/T-type voltage dependent calcium channels in vascular smooth muscle cells (Lu et al., 1996). We can suggest that in the smooth muscle cells of the rat bladder a similar effect takes place.

Role of extracellular calcium for Ang II- and AVP-mediated contractions of smooth muscle cells

The increase of concentration of the extracellular Ca2+ exerts a synergistic effect on Ang II- and AVP-mediated contractions. The raise of the amplitude of contraction is a consequence of increased transmembrane calcium influx due to the higher electrochemical gradient. As a result the intracellular calcium concentration is maintained at the higher level than the level of the resting state. There is evidence that this pattern of variations in calcium concentration contributes to the development of the mechanism of "locking" of the smooth muscle cells (Tanaka et al., 2008). We suppose that the above mentioned significant difference in AUC is due to the manifestation of this mechanism (Tolekova et al., 2010).


The endocrine effects of the peptide ghrelin on various organs and systems are not well examined; however it is known that it stimulates the motility of digestive tract (Tack et al., 2006). On the vascular smooth muscle it exercises a dilatatory influence which is comparable to that caused by adrenomeduline (Wiley & Davenport, 2002). Binding of ghrelin to the its membrane receptors in some tissues triggers signal transduction mechanism via Gq protein and results in activation of PLC and release of IP3 and Ca2+ (Davenport et al., 2005). There are no data in the literature regarding the effects of ghrelin on urinary bladder smooth muscle. The presence of ghrelin receptors on the membranes of detrusor smooth muscle cells is not proven yet. Therefore it is interesting to investigate whether and how ghrelin affects the bladder detrusor and if so by which signal transduction mechanism. Moreover, there is not existing published comparison between the effects of AVP and Ang II on detrusor contractile activity as well as effects of calcium and ghrelin on the smooth-muscle contractions mediated by these peptides.

Does Ghrelin have an effect on a urinary bladder?

The receptors for ghrelin described in the literature mediate their activity with activation of PLC and subsequent increase in concentration of intracellular calcium (Davenport et al., 2005). Therefore, the application of ghrelin on muscle strips of urinary bladder would lead to the occurrence of tonic contractions. During the experiments we found no statistically significant changes in contractile activity after application of ghrelin as compared to the spontaneous activity. The effects of ghrelin are displayed only when it is applied in combination with other peptides – Ang II or AVP. In combination with Ang II, ghrelin reduces its contractile effect on the bladder (Ilieva et al., 2008, a). The combination of ghrelin with AVP leads to similar yet significantly less manifested decrease, especially in the AUC.

Based on these results we can assume that the urinary bladder possesses receptors for ghrelin, different from those in the digestive tract, with respect to the intracellular signaling mechanism to which they are coupled. The significant reduction in the amplitude of Ang II-induced contraction as well as the partial reduction of AVP-provoked contraction after ghrelin application could be explained by the interaction between signal transduction pathways by which the both peptides act. To our knowledge, this is the first in vitro study demonstrated the inhibitory effect of ghrelin on bladder motor activity. Our results were confirmed by Matsuda et coauthors (2011). They showed in experiments in vivo that intracerebroventricular administration of Ghrelin increases bladder capacity dose dependently.

It is likely that ghrelin acts through the second messenger cAMP. Activation of this signal pathway causes relaxation of smooth muscles by decreasing the activity of miosinkinase and stimulating Ca2+-efflux. This effect of ghrelin could be explained with interactions between the two types of transduction pathways, which have opposite effects (Rasmussen & Rasmussen, 1990; Churchill, 1985).

3.2. Gastro-intestinal tract

Angiotensin II

Angiotensin II has potent contractile effect on smooth muscles in the gastro-intestinal tract (GIT). The question for the exact effects of Ang II on GIT remains still opened. Local RAS or parts of it had been found in rat rectum (De Godoy et al., 2006), rat small intestine, and in the guinea pig gall bladder (Leung et al., 1993). The role of Ang II had been confirmed in the development of diseases such as the gastro-esophageal reflux (Fändriks, 2010), incontinence of internal anal sphincter (De Godoy et al., 2006; Rattan et al., 2003), and Crohn's disease (Fändriks, 2010; Wang et al, 1993) as well as other inflammatory and motility disorders of the GIT (Fändriks, 2010).

Most of the effects of Ang II concerning the smooth muscle contractile activity of GIT are associated with AT1 receptors (Fändriks, 2010; Fan et al., 2002; Hawcock & Barnes, 1993; Rattan et al., 2003). AT2 receptors are also described in GIT (Fändriks, 2010; Fan et al., 2002; De Godoy et al., 2006; Hawcock & Barnes, 1993; Ewert et al., 2003; Leung et al., 1993; De Godoy et al., 2002). Although different signaling pathways have been assumed, for example activation of various phosphatases, cGMP -NO system etc. (Ewert et al., 2003; Dinh et al., 2001), their actual signal transduction is not quite elucidated. AT2 receptors are associated with the exchange of water and salts, sodium hydrogen carbonate secretion in the duodenum (Fändriks, 2010) and the secretion of nitric oxide in pig’s jejunum (Ewert et al., 2003). The significance of AT2 receptors for GIT motility has not been established yet. It is supposed that they have the opposite effect of AT1 receptors (Gallinat et al., 2000), but as a factor for the smooth muscle relaxation they had been proved only for the internal anal sphincter (De Godoy et al., 2006; De Godoy & Rattan, 2005).

There is not enough information in the literature, regarding to the comparative characteristics of Ang II - induced responses from the various segments of GIT. Dose - dependent curves, which are commonly used as a method for studying the provoked smooth muscle contractions (Fändriks, 2010; Fan et al., 2002; Hawcock & Barnes, 1993; Leung et al., 1993; Park et al., 1973), could give information about the effective doses and maximal responses, but not a data for other important characteristics of the smooth muscle contractions. The different phases of the contraction in the various segments of the GIT, were not clarified and analyzed by application of a time-parameter analysis, as it was made in the study of the skeletal muscle contraction (Raikova & Aladjov, 2004). For comparison and detailed analysis of Ang II contractile effects of Ang II on the different segments of longitudinal strips from rat GIT we are using again time-parameters.

The amplitudes and integral muscle force of different segments from GIT in our experimental study showed marked correlation (r=0.88, p<0.005). The duodenal muscle strip demonstrated the lowest amplitude and smallest integral force of contraction - 0.55±0.13 g, 41.43±15.52 gs. The amplitudes of the registered angiotensin II-induced contraction from stomach (1.14±0.13 g), jejunum (1.11±0.14 g) and ileum (1.09±0.16 g) are similar and there are not statistically significant differences between them. But stomach integral force (178.09±19.63 gs) is significantly greater than that of duodenum and other intestines and is equally powerful as that of the colon. Under influence of Angiotensin II, rectum developed highest amplitude of contraction 4.74±0.65 g and most powerful integral force - 328.43±75.23 gs.

The analysis of time parameters of Ang II-mediated contractions indicated that the gastric response to Ang II required more time to develop: the time to reach Thc and Tc parameters was 29.09± 2.53 s and 78.18 ± 5.87 s respectively. This tendency for a slower progress of the reaction was maintained during the whole contraction of the stomach and its Tchr was 224.90 ± 18.45s. All of the registered intestinal contractions showed similar values for Thc and Tc parameters. For the remaining two time - parameters - Thr and Tchr, the results from the intestinal contractions were analogous, with exception of the ileac contraction, which Thr (106.33±9.89 s) and Tchr (141.08±9.48 s) were significantly prolonged. After normalization of time-parameter, it was shown that jejunum and colon have similar pattern of contractions and relaxation (Figure 3). The relaxation takes one half of the process and the first and the second part of the contraction are with almost identical proportion, The other parts of GIT - stomach, duodenum and rectum have almost similar pattern of contractions and relaxations. Only ilium differs from these two groups. The relative part of its relaxation was 0.75 from whole duration of process. Application of the time parameters clearly shows the presence of bilateral symmetry in the responses of the gastrointestinal tract.

The amplitude comparison of the Ang II-induced contractions divides the isolated smooth muscle preparations into two groups. The stomach and the small intestines form one group, and the large intestines form another. It is obvious that the large intestines are more sensitive to Ang II and react with more powerful contractions. There is a gradual increase in

Figure 3.

Normalized time-parameters of contractile activity of different GIT segments, induced by Angiotensin II. 1-Thcn, 2-T(c-hc)n and Thrn.

the muscle response to Ang II along the rat intestine, which confirms previous studies of Ang II - provoked intestinal contractions (Ewert et al., 2006). In the literature there are evidences about the uneven distribution of the Ang II receptors in most tissues of the adult organism (Steckelings et al., 2010). Regarding GIT there has been described an unequal density of AT1 receptors (Fändriks, 2010), which could explain the obtained results. From the other side, the duodenal contraction has the smallest amplitude, which strongly differentiates the reaction of the duodenum from the other GIT segments. This could be due to low density of duodenal Ang II receptors and with a local production of NO by the duodenal mucosa (Aihara et al., 2005).

There had been established several transduction pathways of Ang II- induced SMC (Dinh et al., 2001; Romero et al., 1998). The modulating effect of Ang II on different ion currents also had been reported (Chorvatova et al., 1996; Romero et al., 1998). According to Thc and Tc parameters, there is a marked difference between the stomach from the one side, and the intestines from the other. All of the studied intestinal segments showed similar speed of contraction, while the duration of the stomach reaction was far longer. That data suggest a possible transduction pathway for SMC of the stomach, different than in the others GIT segments.

Some authors consider possible competitive interactions between AT1 and AT2 receptors in smooth musculature of the intestine, which supports some previous statements that the magnitude of the response to Ang II depends on the expression of both receptors (Ewert et al., 2006). It had been demonstrated that only AT1 receptors are relevant for the maximum response in ANG-induced contractions (Hawcock & Barnes, 1993; Fändriks, 2010; Fan et al., 2002; Rattan et al., 2003; Ewert et al., 2006; Fändriks, 2010). Despite the existing assumptions that stimulation of AT2 receptors may have the opposite effect than that of AT1 (Gallinat et al., 2000), the role of AT2 receptors for the relaxation phase of the SMC in GIT is not examined. The importance of AT2 receptors for the relaxation of the rectum has been described only (De Godoy et al., 2006; De Godoy & Rattan, 2005). Regarding the time parameters for relaxation, the stomach again showed the slowest response. In this case the ileum indicated significantly prolonged reaction compared to the other intestinal segments. The reason for that difference may be the complete absence or the low density of AT 2 receptors in the ileum (Fändriks, 2010).

In conclusions the observed differences in the Ang II - induced gastro-intestinal contractions may be due to:

  • Variation in the Ang II receptor subtypes distribution. Regarding GIT there has been described an unequal density of Ang II receptors. This uneven distribution of the receptors could explain the differences in the amplitude and duration of Thc of SMC.

  • Counteraction between Ang II receptor subtypes. Competing actions between Ang II receptors have been discussed in the smooth musculature of rat small intestine. The relative receptor expression is a determinant of the magnitude of response to Ang II. This might be of importance for the duration of muscle contraction after reaching the maximal response - expressed by Thr.

  • Activation of various transduction pathways. There is data that Ang II can modulate ionic conductance in distinct tissues. The different duration of the interval between Thc and Tc, as well as Thr may be due to the involvement of some membrane ion channels.

  • Presence of local rennin - angiotensin system and formation of numerous of active angiotensin derivates. It is proven that most tissues are the source, target and degradation site of Ang II. Furthermore, local rennin - angiotensin system or parts of it had been found in rat rectum and rat small intestine. This is another possibility which could explain the obtained data about the phase of relaxation and force of SMC.

  • The use of time - parameters significantly contributes to the analysis of the contraction process and permits a good comparison of the Ang II – induced responses. Presentation of the time parameters as part of the total contraction normalization) gives an idea for the development of the process in the different time intervals.

  • The obtained results provide a direction for further research work on Ang II-mediated contractions of GIT and for clarifying the exact role of the AT1 and AT2 receptors in the different phases of SMC.

Ang II – provoked rectal response. Comparison with the urinary bladder response

The application of Ang II on the rectal preparation caused a development of expressed tonic contraction, which amplitude and integral muscle force were significantly greater than those of the bladder. The higher amplitude is achieved at the expense of the second half of the contraction. The higher values of the absolute and normalized time – parameters for this interval are the evidence. The difference in the total muscle mass of the preparations significantly contributes for these distinctive force parameters. It is worth noted, that the time-parameters (absolute and normalized) of Ang II – mediated bladder and rectal SMC, with the exception of T(c-hc) parameter, do not indicate significant differences (Figure 4). This proves the suggestion that in the urinary bladder and rectum the Ang II - mediated contractions are developed by similar mechanisms. Moreover, this assumption is an indirect evidence for an approximately equal density of Ang II receptors in these two organs. The uniformity of response to Ang II is supported by the fact that it the rectum a local renin-angiotensin system has also been established (De Godoy & Rattan, 2006). It could be considered again that the locally generated metabolites of Ang II contribute for this pattern of the contraction process.

Figure 4.

Normalized time-parameters of urinary bladder and rectum Ang II – induced contractions. All of the normalized time-intervals were calculated as a relative part from Tchr.

Does AVP have an importance for the motility of the gastro-intestinal tract?

Dose-dependent effects of AVP on gastro-intestinal tract from different species were observed, but regarding the rectal musculature the information is insufficient and controversial (Ohlsson et al., 2006). AVP has been shown to increase the gastric and duodenal motility in humans and rabbits (Ohlsson et al., 2006; Li et al., 2007), as well as colonic peristalsis, but the expression of the AVP receptors in intestine has not been examined yet (Ohlsson et al., 2006). Some authors have demonstrated that AVP increase the gastro-intestinal motility via the oxytocin OT1 receptors, but the experiment is only for stomach and duodenum from rabbits (Li et al., 2007).

In our study, the application of AVP does not significantly alter the characteristics of the spontaneous phasic contractile activity of gastro-intestinal segments except this of stomach. This could be explained with the absence of AVP receptors type V1, which are present in the urinary bladder. In rectal musculature V2 receptors could be presented – in such a case, the rectum as a terminal department of gastro-intestinal tract shows analogy with the distal and the collecting tubules of the kidneys. This is still an assumption that remains to be investigated.


The mechanical activity of the gallbladder of conscious dogs consisted of spontaneous rhythmic contractions with a frequency of 2 to 5 cpm. Fluctuations of the tone were also observed. Bolus injection of cholecystokinin octapeptide i.v. produced a dose-dependent increase in gallbladder pressure (Figure 5A). Atropine decreased gallbladder pressure and reduced or even abolished the cholecystokinin action (Figure 5B). Hexamethonium led to gallbladder relaxation and also greatly reduced the gallbladder response to cholecystokinin octapeptide (Figure 5C).

The mechanisms through which atropine or hexamethonium inhibit cholecystokinin-produced gallbladder contractions under in vivo conditions are not understood. One possible explanation might be that the excitatory effect of cholecystokinin on the gallbladder is mediated by acetylcholine release from cholinergic neurons at pre- and post- ganglionic level. Another possibility is that atropine and/or hexamethonium are able to block the release of endogenous cholecystokinin from the endocrine cells or neurons. This suggestion is supported by the fact that vagotomy abolish gallbladder response to cholecystokinin after acidification (Fried et al., 1983), infusion of fat into the duodenum (Magee et al., 1984) or after drinking water (Sundler et al., 1977). The release of CCK in the circulation in response to fat or other meals is also reduced after vagotomy or atropine. It is also possible that atropine or hexamethonium blockade of cholinergic input to the gallbladder may unmask the release of neuronal inhibitory influence which could then compete with the release of CCK. Such inhibitory agents could be somatostatin and vasoactive intestinal peptide (Lenz et al., 1993; Milenov et al., 1995).


It has been reported that in the uteri of a number of species, local production of Ang II and the enzymes for its synthesis are present. Besides the proven contractile effect of Ang II on the uterine arteries, research in this area showed that myometrium is also sensitive to the effect of this octapeptide (Keskil et al., 1999).

Figure 5.

CCK-8 (2.5; 5 and 10 ng/kg i.v.)-induced gallbladder pressure before (A) and after atropine (B) (20 μg/kg i.v.) or hexamethonium (C) (1 mg/kg i.v.). Means ± S.E.M. of 12 experiments in 6 conscious dogs are presented, P < 0.01.

There is substantial evidence for the involvement of AVP in conditions of uterine hyperactivity. Even more, it has been shown that the human myometrium is more sensitive to AVP than to oxytocin (Bossmar et al., 2007).

Ang II at concentration of 1 µmol induced tonic contraction with maximum amplitude of 6.00 ± 0.22 g and an integral force of muscle contraction of 1150.00 ± 614.70 gs. AVP applied in the same concentration as Ang II induced tonic contractions with amplitude of 6.61 ± 0.39 g (n = 8) and an integral force of muscle contraction of 7245.00 ±901.00 gs. The duration of the AVP-induced responses was several times greater than those of Ang II and the recording of AVP-mediated contractions was stopped on the 30th minute without achievement of Tchr parameter.

Our experiment confirmed the contractile effect of these two peptides on the myometrium, which is in accordance with the results of other authors working on the same issues (Anouar et al., 1996; Chan et al., 1996; Keskil et al., 1999).

The contractions induced by both peptides have similar amplitudes, but they are with different duration and characteristics. The registered AVP - provoked uterine responses were found to have a sustained oscillating character Figure 6). When analyzed by mathematical modeling such contractions were recognized as underdamped process - the system tries to establish a stable level different from the baseline (Yankov, 2009). The differences in the developed contractions may be due to split of the classical or inclusion of additional transduction pathway for each of the studied peptides. Both of them have several main groups of receptors. The receptors for Ang II are AT1 and AT2 (De Gasparo et al., 2000), while the receptors for AVP are V1a, V1b and V2 (Petersen, 2006).

Figure 6.

Original record of vasopressin-induced uterine contraction.

To establish the importance of these receptors for the uterine muscle contraction will be the subject of our next experiments. However, several interesting facts immerge:

First – the constrictor effect of Ang II is associated with AT1 receptors, but the uterus is one of the few organs with a. uterina inferior where AT2 receptors are predominant (Keskil et al., 1999). AT2 receptors are mainly regarded to oppose the effects of AT1 and cause dilation, blood pressure reduction, nitric oxide production (Hannan et al., 2003). Perhaps the significantly shorter phase of contraction and relaxation was due to their activation under the influence of Ang II in the uterus. Second – the constrictor effect of AVP is realized by V1a receptors which are found in uterine arteries. With regard to the contractile response of the myometrium, however, there are statements that the resulting contraction from the AVP influence is due to activation of other receptors, different from the mentioned above (Anouar et al., 1996). Some authors go even further and argue that AVP accomplish its effect on uterine musculature by OT receptors, which have big similarity with V1 receptors (Chan et al., 1996).

Considering that both peptides are released from supraoptic nuclei in the hypothalamus and that they have a powerful contractile effect on the smooth muscle, it is appropriate to search a closer connection between them in preparing the uterus for pregnancy and labor. Probably these two peptides act synchronously which potentiate their own effects (Douglas et al.,2001).

Studies on rats show that AVP is more potent uterotonic agent than OT in non pregnant condition (Bossmar et al., 2007) and during parturition OT predominantly promotes uterine contractions, while AVP is more important for vasoconstriction, thus reducing the bleeding after delivery (Chan et al., 1996; Douglas et al.,2001).

The study of Ang II – and AVP – mediated uterine contractions contributes considerably for the revealing of the mechanisms that generate and modulate uterine activity. This could be beneficial for a better understanding and control of myometrial dysfunction.



This work was supported by Grant DDVU-02-24/2010 from the National Science Fund, Sofia, Bulgaria and Grant MF - 1/2010 from Medical Faculty, Trakia University.


  1. 1. AguileraG.1994Regulation of pituitary ACTH secretion during chronic stress. Front Neuroendocrinol.,1532150
  2. 2. AiharaE.KagawaS.HayashiM.TakeuchiK.2005ACE inhibitor and AT1 antagonist stimulate duodenal HCO3- secretion mediated by a common pathway- involvement of PG, NO and bradykinin. J Physiol Pharmacol, 563391406
  3. 3. Allen AM, MacGregor DP, McKinley MJ, Mendelsohn FA1999Angiotensin II receptors in the human brain. Regul Pept, 7917
  4. 4. AnderssonK. E.ArnerA.2004Urinary bladder contraction and relaxation: physiology and pathophysiology. Physiol Rev, 84935986
  5. 5. AnderssonK. E.HedlundH.StahlM.1992Contractions induced by angiotensin I, angiotensin II and bradykinin in isolated smooth muscle from the human detrusor. Acta Physiol Scand, 1453253259
  6. 6. AnderssonK. E.HustedS.MattiassonA.Maller-MadsenB.1982Atropine resistance of trasmurally stimulated isolated human bladder muscle. Urol Res, 15355358
  7. 7. AnouarA.ClergetM.DurrouxT.BarberisC.GermainG.1996Comparison of vasopressin and oxytocin receptors in the rat uterus and vascular tissue. Eur J Pharmacol, 30818796
  8. 8. ArmsteadW.2001Vasopressin-induced protein kinase C-dependent superoxide generation conributes to ATP- sensitive potassium channel but not calcium- sensitive potassium channel function impairment after brain injury. Stroke, 32614081414
  9. 9. BarassinS.KalsbeekA.SaboureauM.BothorelB.Vivien-RoelsB.MalanA.BuijsR. M.PevetP.2000Potentiation effect of vasopressin on melatonin secretion as determined by trans-pineal microdialysis in the Rat. J Neuroendocrinol., 121618
  10. 10. BeckeC.ThiebotM. H.TouitouY.HamonM.CesselinF.BenolielJ. J.2001Enhanced cortical extracellular levels of cholecystokinin-like material in a model of anticipation of social defeat in the rat. J Neurosci 21262269
  11. 11. BerridgeM.2008Smooth muscle cell calcium activation mechanisms. J Physiol, 58650475061
  12. 12. Bosch OJ, Neumann ID2008Brain vasopressin is an important regulator of maternal behavior independent of dams’ trait anxiety. Proc Natl Acad Sci U S A,105441713944
  13. 13. BossmarT.OsmanN.ZilahiE.HajM.NowotnyN.ConlonJ.2007Expression of the oxytocin gene, but not the vasopressin gene, in the rat uterus during pregnancy: influence of oestradiol and progesterone. J Endocrinol, 193121126
  14. 14. BrileyE. M.LolaitS. J.AxelrodJ.FelderC. C.1994The cloned vasopressin 1areceptor stimulates phospholipase A2, phospholipase C, and phospholipase D through activation of receptor-operated calcium channels. Neuropeptides, 27: 63 EOF74 EOF
  15. 15. BroglioF.ArvatE.BensoA.PapottiM.MiccioliG.DeghenghiR.GhigoE.2002Ghrelin: Endocrine and Non-endocrine Actions J Ped Endocrinol & Metab, 1512191227
  16. 16. BroglioF.GotteroC.ArvatE.GhigoE.2003Endocrine and Non-endocrine of Ghrelin. Horm Res, 59109117
  17. 17. BurnstockG.1990In: Neurobiology of Incontinence: Innervation of bladder and bowel. Ciba Foundation Symposium 151226Chichester, Wiley.
  18. 18. Callahan SM, Creed KE1986Non-cholinergic neurotransmission and the effects of peptides on the urinary bladder of guinea-pigs and rabbits. J Physiol, 374103115
  19. 19. CantorP.1986Evaluation of a radioimmunoassay for cholecystokinin in human plasma. Scand J Clin Lab Invest, 46213221
  20. 20. ChanW.WoN.ManningM.1996The role of oxytocin receptors and vasopressin 1areceptors in uterine contractions in rats: implications for tocolytic therapy with oxytocin antagonists. Am J Obstet Gynecol, 175(5): 1331 EOF5 EOF
  21. 21. Chen TF, Doyle PT & Ferguson DR1994Inhibition in the human urinary bladder by gamma-amino-butyric acid. Br J Urol, 73250255
  22. 22. Chiu AT, Smith RD, Timmermans PB1994Defining Angiotensin Receptor Subtypes. In: J.M. Saavedra & P.B. Timmermans Eds.), Angiotensin Receptors 1st edition, 49-65). New York: Springer-Verlag.
  23. 23. ChorvatovaA.Gallo-PayetN.CasanovaC.MDPayet1996Modulation of membrane potential and ionic currents by the AT1 and AT2 receptors of angiotensin II. Cell Signal, 8852532
  24. 24. Churchill PC1985Second messengers in renin secretion. Am J Physiol Renal Physiol, 249: F17584
  25. 25. CohenS. L.KnightM.CATammingaChase. T. N.1982Cholecystokinin-octapeptide effects on conditioned-avoidance behavior, stereotypy and catalepsy. Eur J Pharmacol 83213222
  26. 26. Compaan JC, Buijs RM, Pool CW, De Ruiter AJ, Koolhaas JM1993Differential lateral septal vasopressin innervation in aggressive and nonaggressive male mice. Brain Res Bull., 301216
  27. 27. Crankshaw DJ1989Arg8) vasopressin-induces contractions of rabbit urinary bladder smooth muscle. Eur J Pharmacol, 173(2-3): 183-8.
  28. 28. Crawley JN, Corwin RL1994Biological actions of cholecystokinin. Peptides, 154731755
  29. 29. Crawley JN1992Subtype-selective cholecystokinin receptor antagonists block cholecystokinin modulation of dopamine-mediated behaviors in the rat mesolimbic pathway. J Neurosci, 1233803391
  30. 30. CrespiF.CorsiM.ReggianiA.RattiE.GaviraghiG.2000Involvement of cholecystokinin within craving for cocaine: role of cholecystokinin receptor ligands. Exp Opin Invest Drugs, 922492258
  31. 31. CroweR.BurnstockG.1989A histochemical and immuno-histochemical study of the autonomic innervation of the lower urinary tract of the female pig. Is the pig a good model for the human bladder and urethra? J Urol, 141414422
  32. 32. DateY.NakazatoM.HashiguchiS.DezakiK.MSMondalHosoda. H.KojimaM.KangawaK.ArimaT.MatsuoH.YadaT.MatsukuraS.2002Ghrelin is present in pancreatic alpha-cells of humans and rats and stimulates insulin secretion. Diabetes, 511124129
  33. 33. DavenportA. P.BonnerT. I.FoordS. M.HarmarA. J.NeubigR. R.PinJ. P.SpeddingM.KojimaM.KangawaK.2005International Union of Pharmacology. LVI. Ghrelin Receptor Nomenclature, Distribution and Function. Pharmacol Rev, 57541546
  34. 34. De GasparoM.CattK.InagamiT.WrightJ.UngerT.2000International union of pharmacology. XXIII. The angiotensin II receptors. Pharmacol Rev, 52341572
  35. 35. MADe GodoyRattan. S.2005Autocrine regulation of internal anal sphincter tone by renin-angiotensin system: comparison with phasic smooth muscle. Am J Physiol Gastrointest Liver Physiol, 289(6): G116475b.
  36. 36. MADe GodoyRattan. S.2006Angiotensin-converting enzyme and angiotensin II receptor subtype 1 inhibitors restitute hypertensive internal anal sphincter in the spontaneously hypertensive rats. J Pharmacol Exp Ther, 318272534a.
  37. 37. MADe GodoyDunn. S.RattanS.2004Evidence for the role of angiotensin II biosynthesis in the rat internal anal sphincter tone. Gastroenterology, 127112738
  38. 38. MADe GodoyRattan. S.2006Translocation of AT1- and AT2-receptors by higher concentrations of angiotensin II in the smooth muscle cells of rat internal anal sphincter. J Pharmacol Exp Ther, 3193108895
  39. 39. De Groat WC, Booth AM1984In: Peripheral Neuropathy: Autonomic systems to the urinary bladder and sexual organs. P.J. Dyck, P.K. Thomas, E.H. Lambert & R. Bunge (eds), Philadelphia, W.B. Saunders, 285299
  40. 40. De Groat WC, Booth AM1993In: Nervous control of the urogenital system: Synaptic transmission in pelvic ganglia. Maggi CA (ed), Harwood Academic Publ, Chur, 291347
  41. 41. De GroatW. C.KawataniM.1985Neural control of the urinary bladder: Possible relationship between peptidergic inhibitory mechanisms and detrusor instability. Neurourol Urodyn, 4285300
  42. 42. DegenL.MatzingerD.DreweJ.BeglingerC.2001The effect of cholecystokinin in controlling appetite and food intake in humans. Peptides, 2212651269
  43. 43. DehpourA. R.KivajG. R. T.DelfanA.ShahrokhiM.1997The effects of lithium, indomethacine and neomycin on vassopresin-inducted contractions in rat urinary bladder. Gen Pharmacol, 285777780
  44. 44. Dinh DT, Frauman AG, Johnston CI, Fabiani ME2001Angiotensin receptors: distribution, signalling and function. Clin Sci (Lond), 100548192
  45. 45. Dixon JS, Jen PY, Gosling JA1997A double-label immunohisto-chemical study of intramural ganglia from the human male urinary bladder neck. J Anat, 190125134
  46. 46. Dornan WA, Malsbury CW1989Peptidergic control of male sexual behavior: the effects of intracerebral injections of substance P and cholecystokinin. Physiol Behav, 4654756
  47. 47. DouglasA.ScullionS.AntonijevicI.BrownD.RussellJ.LengG.2001Uterine contractile activity stimulates supraoptic neurons in term pregnant rats via a noradrenergic pathway. Endocrinology, 142263344
  48. 48. Downie JW1981The autonomic pharmacology of the urinary bladder and urethra: a neglected area. Trends Pharmacol Sci, 2163165
  49. 49. DufresneM.SevaC.FourmyD.2006Cholecystokinin and gastrin receptors. Physiol Rev, 863805847
  50. 50. EvaC.ObertoA.MeleP.SerraM.BiggioG.2006Role of brain neuroactive steroids in the functional interplay between the GABAA and the NPY-Y1 receptor mediated signals in the Amygdala. Pharmacology Biochemistry and Behavior, 844568580
  51. 51. EwertS.LaesserM.JohanssonB.HolmM.AnemanA.FandriksL.2 EOF2003The angiotensin II receptor type 2 agonist CGP 42112A stimulates NO production in the porcine jejunal mucosa. BMC Pharmacol, 3:2.
  52. 52. EwertS.SpakE.OlbersT.JohnssonE.EdeboA.FändriksL.2006Angiotensin II induced contraction of rat and human small intestinal wall musculature in vitro. Acta Physiol (Oxf), 18813340
  53. 53. FanY. P.RNPuriRattan. S.2002Animal model for angiotensin II effects in the internal anal sphincter smooth muscle: mechanism of action. Am J Physiol Gastrointest Liver Physiol, 282(3): G4619
  54. 54. FändriksL.2010The angiotensin II type 2 receptor and the gastrointestinal tract. J Renin Angiotensin Aldosterone Syst., 111438
  55. 55. FeherE.VajdaJ.1981Sympathetic innervation of the urinary bladder. Acta Morphol Acad Sci Hung, 292735
  56. 56. FerensD.YinL.Ohashi-DoiK.HabgoodM.BronR.BrockJ.GaleJ.FurnessJ.2010Evidence for functional ghrelin receptors on parasympathetic preganglionic neurons of micturition control pathways in the rat. Clin Exp Pharmacol Physiol, 379926932
  57. 57. FittsD. A.StarbuckE. M.RuhfA.2000Circumventricular organs and Ang II-induced salt appetite: blood pressure and connectivity. Am J Physiol, Reg Integ Comp Physiol, 279: R2277R2286.
  58. 58. FrankE.LandgrafR.2008The vasopressin system--from antidiuresis to psychopathology. Eur J Pharmacol.,583(2-3):226 EOF42 EOF
  59. 59. Fried GM, Ogden WD, Greely GG1983Correlation of release and action of cholecystokinin in dogs before and after vagotomy. Surgery, 936786792
  60. 60. FujinoK.InuiA.AsakawaA.KiharaN.FujimuraM.FujimiyaM.2003Ghrelin induced fasted motor activity of the gastrointestinal tract in conscious fed rats. J Physiol, 5501227240
  61. 61. GabellaG.UveliusB.1990Urinary bladder of rat: fine structure of normal and hypertrophic musculature. Cell Tissue Res, 2626779
  62. 62. GagnonD. J.SiroisP.1972The rat isolated colon as a specific assay organ for angiotensin. Br J Pharmacol, 4618993
  63. 63. GallinatS.BuscheS.RaizadaM. K.SumnersC.2000The angiotensin II type 2 receptor: an enigma with multiple variations. Am J Physiol Endocrinol Metab, 278(3): E35774
  64. 64. GarcíaM.LópezM.AlvarezC.CasanuevaF.Tena-SempereM.DiéguezC.2007Role of ghrelin in reproduction. Reproduction, 1333531540
  65. 65. GeJ.BarnesN. M.1996Alterations in angiotensin AT1 and AT2 receptor subtype levels in brain regions from patients with neurodegenerative disorders. Eur J Pharmacol, 297299306
  66. 66. GeorgievV.YonkovD.1985Participation of angiotensin II in learning and memory: I. Interaction of angiotensin II with saralasin.Meth Find Exp Clin Pharmacol, 7415418
  67. 67. GhigoE.BroglioF.ArvatE.MaccarioM.PaotiM.MuccioliG.2005Ghrelin: more than a natural GH secretagoue and/or an orexigenic factor. Clin Endocrinol, 62117
  68. 68. Goncharuk VD, Buijs RM, Jhamandas JH, Swaab DF2011Vasopressin (VP) and neuropeptide FF (NPFF) systems in the normal and hypertensive human brainstem. J Comp Neurol, 519193124
  69. 69. Goodson JL, Bass AH2001Social behavior functions and related anatomical characteristics of vasotocin/vasopressin systems in vertebrates. Brain Res Brain Res Rev, 35324665
  70. 70. GulubovaM. V.HadjipetkovP.SivrevD.IlievaG.2012Endocrine cells in the human common bile duct in patients with obstructive jaundice. Hepatogastroenterology, 591132630
  71. 71. HadzhibozhevaP.IlievR.TolekovaA.IlievaG.TrifonovaK.SandevaR.TsokevaZ.KalfinR.2009Effects of some neuropeptide on detrusor strips from rat urinary bladder. Bulg J Vet Med, 126772
  72. 72. HannanR.DavisE.WiddopR.2003Functional role of angiotensin II AT2 receptor in modulation of AT1 receptor-mediated contraction in rat uterine artery: involvement of bradykinin and nitric oxide. Br J Pharmacol, 140598795
  73. 73. Harper AA, Raper HS1943Pancreozymin, a stimulant of the secretion of pancreatic enzymes in extracts of the small intestine. J Physiol, 102115125
  74. 74. HashimotoH.UetaY.2011Central effects of ghrelin, a unique peptide, on appetite and fluid/water drinking behavior. Curr Protein Pept Sci., 1242807
  75. 75. Hawcock AB, Barnes JC1993Pharmacological characterization of the contractile responses to angiotensin analogues in guinea-pig isolated longitudinal muscle of small intestine. Br J Pharmacol, 108411505
  76. 76. HelmG.OwmanC.RosengrenE.SjobergN. O.1982Regional and cyclic variations in catecholamine concentration of the human fallopian tube. Biol Reprod, 26553558
  77. 77. HermesM. L.RuijterJ. M.KlopA.BuijsR. M.RenaudL. P.(2002000Vasopressin increases GABAergic inhibition of rat hypothalamic paraventricular nucleus neurons in vitro. J Neurophysiol, 83270511
  78. 78. HokfeltT.RehfeldJ. F.SkirbollL.IvemarkB.GoldsteinM.MarkeyK.1980Evidence for coexistence of dopamine and CCK in meso-limbic neurones. Nature, 285476478
  79. 79. Holmes CL, Patel BM, Russell JA, Walley KR2001The physiology of vasopresin relevant to the management of septic shock. Chest,1209891002
  80. 80. IlievaG.TolekovaA.SandevaR.TrifonovaK.TsokevaZh.GanevaM.2008Influence of ghrelin on Angiotensin II mediated contraction of smooth muscle strips from urinary bladder. Trakia J Sci, 627781a.
  81. 81. IlievaG.TolekovaA.SandevaR.TrifonovaK.TsokevaZh.GanevaM.MihovaZ.TolevA.ZezovskiS.2008Role of transmembrane calcium current in angiotensin II- mediated contraction of detrusor organ strips from rat urinary bladder. Bulg J Vet Med, 1128994
  82. 82. InuiA.AsakawaA.BowersC. Y.MantovaniG.LavianoA.MeguidM.FujimiyaM.2004Ghrelin, aetite, and gastric motility: the emerging role of the stomach as an endocrine organ. The FASEB Journal,18439456
  83. 83. IvyA. C.OldbergE.1928A hormone mechanism of gall bladder contraction and evacuation. Am J Physiol, 86599613
  84. 84. JanigW.Mc LachlanE. M.1987Organization of lumbar spinal outflow to distal colon and pelvic organs. Physiol Rev, 6713321404
  85. 85. Josselyn SA, Vaccarino FJ1996Acquisition of conditioned reward blocked by intra-accumbens infusion of PD-140548, a CCKA receptor antagonist. Pharmacol Biochem Behav, 55439444
  86. 86. KalraS.DubeM.PuS.XuB.HorvathT. P.KalraS.1999Interacting appetite-regulating pathways in the hypothalamic regulation of body weight. Endocrine Reviews, 20168100
  87. 87. KalsbeekA.BuijsR. M.EngelmannM.WotjakC. T.LandgrafR.1995In vivo measurement of a diurnal variation in vasopressin release in the rat suprachiasmatic nucleus. Brain Res, 682(1-2):75 EOF82 EOF
  88. 88. KalsbeekA.FliersE.MAHofmanSwaab. D. F.BuijsR. M.2010Vasopressin and the output of the hypothalamic biological clock. J Neuroendocrinol.,22536272
  89. 89. KamP.WilliamsS.YoongF.2004Vasopressin and terlipressin: pharmacology and its clinical relevance. Anaesthesia, 599931001
  90. 90. KangK. S.YahashiS.MatsudaK.2011The Effects of Ghrelin on Energy Balance and Psychomotor Activity in a Goldfish International. Journal of Peptides, 19
  91. 91. KeskilZ.BayramM.ErcanZ.TürkerR.1999The contribution of nitric oxide and endothelins to angiotensin: II. Evoked responses in the rat isolated uterus smooth muscle. Gen Pharmacol, 33430712
  92. 92. KimS.AwaoH.2011Molecular and Cellular Mechanisms of Angiotensin II-Mediated Cardiovascular and Renal Diseases. Pharmacological reviews; 521124
  93. 93. KimS.IwaoH.2000Molecular and cellular mechanisms of angiotensin II-mediated cardiovascular and renal diseases. Pharmacol Rev, 521134
  94. 94. KojimaM.KangawaK.2005Ghrelin: Structure and Function. Physiol Rev., 85495522
  95. 95. KolaB.HubinaE.TucciS.KirkhamT. C.GarciaE. A.MitchellS. E.WilliamsL. M.HawleyS. A.HardieD. G.GrossmanA. B.KorbonitsM.2005Cannabinoids and ghrelin have both central and peripheral metabolic and cardiac effects via AMP-activated protein kinase. Journal of Biological Chemistry, 280262519625201
  96. 96. KovácsG. L.BohusB.VersteegD. H. G.KloetE. R.WiedD.1979Effect of oxytocin and vasopressin on memory consolidation: sites of action and catecholaminergic correlates after local microinjection into limbic-midbrain structures. Brain Res, 175303314
  97. 97. LasanenL. T.TammelaT. L.KallioinenM.WarisT.1992Effect of acute distension on cholinergic innervation of the rat urinary bladder. Urol Res, 205962
  98. 98. LeeH.WangG.EnglanderE. W.KojimaM.GreeleyG.2002Ghrelin, a new gastrointestinal endocrine peptide that stimulates insulin secretion: enteric distribution, ontogeny, influence of endocrine, and dietary manipulations. Endocrinology, 1431185190
  99. 99. LenkeiZ.PalkovitsM.CorvolP.Lorens-CortesC.1997Expression of angiotensin type-1 (AT1) and type-2 (AT2) receptor mRNA in the adult rat brain: A functional neuroanatomical review. Front Neuroendocrinol, 18383439
  100. 100. LenzH. J.ZimmermanF. G.MessmerB.1993Regulation of canine gallbladder motility by brain peptides. Gastroenterology, 104616781685
  101. 101. LeungE.RaJ. M.WalshL. K.ZeitungK. D.EglenR. M.1993Characterization of angiotensin II receptors in smooth muscle preparations of the guinea pig in vitro. J Pharmacol Exp Ther, 267315218
  102. 102. LiL.KongX.LiuH.LiuC.2007Systemic oxytocin and vasopressin excite gastrointestinal motility through oxytocin receptor in rabbits. Neurogastroenterol & Motility, 1910839844
  103. 103. Liddle RA1997Cholecystokinin cells. Annu Rev Physiol, 59221242
  104. 104. Lieverse RJ, Masclee AA, Jansen JB, Rovati LC, Lamers CB1995Satiety effects of the type A CCK receptor antagonist loxiglumide in lean and obese women. Biol Psychiatry, 375331335
  105. 105. LimC. T.KolaB.KorbonitsM.GrossmanA. B.2010Ghrelin’s role as a major regulator of appetite and its other functions in neuroendocrinology. Prog. Brain Res., 182189205
  106. 106. LindbergB. F.NilssonL. G.HedlundH.StahlM.AnderssonK. E.1994Angiotensin I is converted to angiotensin II by a serine protease in human detrusor smooth muscle. Am J Physiol, 266 (6): R18611867
  107. 107. LuH.FernR.LuthinD.LindenJ.LiuL.CohenCh.BarrettP.1996Angiotensin II stimulates T-type Ca2+ channel currents via activation of a G protein, Gi. Am J Physiol, 271 (4): C13401349
  108. 108. LuS.GuanJ.WangQ.UeharaK.YamadaS.GotoN.DateY.NakazatoM.KojimaM.KangawaK.ShiodaS.2002Immunocytochemical observation of ghrelin-containing neurons in the rat arcuate nucleus. Neurosci Lett, 3213157160
  109. 109. LuoB.CheuJ. W.SiegelA.1998Cholecystokinin B receptors in the periaqueductal gray potentiate defensive rage behavior elicited from the medial hypothalamus of the cat. Brain Res, 7962737
  110. 110. MageeD. F.NaruseS.PapA.1984Vagal control of gallbladder contraction. J Physiol, 3556570
  111. 111. MelloV.SchwabU.LaaksonenD.RauramaaR.GyllingH.AtalayM.PulkkinenL.UusitupaM.2008Expression of ghrelin gene in peripheral blood mononuclear cells and plasma ghrelin concentrations in patients with metabolic syndrome. Eur J Endocrinol, 1584499510
  112. 112. Maggi AC1991The role of peptides in the regulation of the micturition reflex: an update. Gen Pharmacol, 22124
  113. 113. Maggi AC1995Tachykinins and calcitonin gene-related peptide CGRP) as cotransmitters released from peripheral ending of sensory nerves. Prog Neurobiol, 45198
  114. 114. Markowski, VP, Hull EM1995Cholecystokinin modulates mesulimbic dopaminergic influences on male rat copulatory behavior. Brain Res, 699266274
  115. 115. MatsudaK.KangK.SakashitaA.YahashiS.VaudryH.2011Behavioral effect of neuropeptides related to feeding regulation in fish. Annals of the New York Academy of Sciences, 1220111712
  116. 116. MatsutaY.NagaseK.IshidaH.TanaseK.AkinoH.YokoyamaO.2011Peripheral ghrelin administration increases bladder capacity without affecting the bladder contraction pressure or electroencephalogram in rats. Available:
  117. 117. McKinley MJ, Albiston AL, Allen AM, Mathai ML, May CN, McAllen RM, Oldfield BJ, Mendelsohn FAO, Chai SY2003The brain renin-angiotensin system: location and physiological roles. The International Journal of Biochemistry & Cell Biology, 35901918
  118. 118. MilenovK.RakovskaA.KalfinR.1995Effects of cholecystokinin on the gallbladder motility: Interaction with somatostatin and vasoactive intestinal peptide. Acta Physiol Pharmacol Bulg 216776
  119. 119. MilosevićV. L.StevanovićD. M.NesićD. M.Sosić-JurjevićB. T.AjdzanovićV. Z.StarcevićV. P.SeversW. B.2010Central effects of ghrelin on the adrenal cortex: a morphological and hormonal study. Gen Physiol Biophys, 292194202
  120. 120. MiyazakiM.TakaiS.2006Tissue angiotensin II generating system by angiotensin-converting enzyme ans chimase. J Pharmacol Sci,10053917
  121. 121. MladenovM.HristovK.DuridanovaD.2006Ghrelin Suression of Potassium Currents in Smooth Muscle Cells of Human Mesenteric Artery. Gen Physiol Biophys, 25333338
  122. 122. MuttV.1980Cholecystokinin: Isolation, structure and function. In: Glass GBJ, editor. Gastrointestinal Hormones. New York: Raven Press. 169203
  123. 123. OhlssonB.BjörgellO.EkbergO.DarwicheG.2006The oxytocin/vasopressin receptor antagonist atosiban delays the gastric emptying of a semisolid meal compared to saline in human. BMC Gastroenterol,16611
  124. 124. OtsukaA.BarnesK. L.FerrarioC. M.1986Contribution of area postrema to pressor actions of angiotensin II in dog. Am J Physiol, 251: H538H546.
  125. 125. ParkW. K.RegoliD.RiouxF.1973Characterization of angiotensin receptors in vascular and intestinal smooth muscles. Br J Pharmacol, 482288301
  126. 126. PaulM.PoyanMehr. A.KreutzR.2006Physiology of local renin-angiotensin systems. Physiol Rev, 863747803
  127. 127. PetersenM.2006The effect of vasopressin and related compounds at 1aand V2 receptors in animal models relevant to human disease. Basic Clin Pharmacol Toxicol, 99(2): 96 EOF103 EOF
  128. 128. PetkovG.HenerT.BonevA.HerreraG.NelsonM.2001Low levels of KATP channel activation decrease excitability and contractility of urinary bladder. Am J Physiol Regul Integr Comp Physiol, 280 (5): R1427R1433.
  129. 129. PhullH.SalkiniM.EscobarC.PurvesT.ComiterC. V.2007The role of angiotensin II in stress urinary incontinence: A rat model. Neurourol Urodyn, 2618188
  130. 130. PickarJ.HillJ.KaufmanM. P.1993Stimulation of vagal afferents inhibits locomotion in mesencephalic cats. Journal of Applied Physiology, 741103110
  131. 131. Raikova RT, Aladjov HT2004Simulation of the motor units control during a fast elbow flexion in the sagittal plane. J Electromyogr Kinesiol, 14222738
  132. 132. RasmussenH.RasmussenJ. E.1990Calcium as intracellular messenger: From simplicity to Complexity. Curr Top Cell Regul, 311109
  133. 133. RattanS.RNPuriFan. Y. P.2003Involvement of rho and rho-associated kinase in sphincteric smooth muscle contraction by angiotensin II. Exp Biol Med (Maywood), 228897281
  134. 134. RomeroF.BASilvaNouailhetas. V. L.AboulafiaJ.1998Activation of Ca2+-activated K+ (maxi-K+) channel by angiotensin II in myocytes of the guinea pig ileum. Am J Physiol, 274(4 Pt 1): C98391
  135. 135. Romine MT & Anderson GF1985Evidence for oxytocin receptors in the urinary bladder of the rabbit. Can J Physiol Pharmacol, 634287291
  136. 136. SavaskanE.2005The Role of the Brain Renin-Angiotensin System in neurodegenerative disorders. Current Alzheimer Research, 212935
  137. 137. SchneiderL. H.AlpertJ.IversenS. D.1983CCK-8 modulation of mesolimbic dopamine: antagonism of amphetamine-stimulated behaviors. Peptides, 4749753
  138. 138. SekiT.YokoshikiH.SunagawaM.NakamuraM.SperelakisN.1999Angiotensin II stimulation of Ca2+-channel current in vascular smooth muscle cells is inhibited by lavendustin-A and LY-294002. Pflugers Arch- Eur J Physiol, 437317323
  139. 139. Shimuta SI, Borges AC, Prioste RN, Paiva TB1999Different pathways for Ca2+ mobilization by angiotensin II and carbachol in the circular muscle of the guinea-pig ileum. Eur J Pharmacol, 36715966
  140. 140. ShokeiK.HiroshiI.2011Molecular and Cellular Mechanisms of Angiotensin II-Mediated Cardiovascularand Renal Diseases. Pharmacol Rev, 5211134
  141. 141. SibiliaV.PaganiF.RindiG.LattuadaN.RapettiD.De LucaV.CampaniniN.BulgarelliI.LocatelliV.GuidobonoF.NettiC.2008Central ghrelin gastroprotection involves nitric oxide/prostaglandin cross-talk. Br J Pharmacol.,1543688697
  142. 142. Sibley GNA1984A comparison of spontaneous and nerve-mediated activity in bladder muscle from man, pig and rabbit. J Physiol (Lond), 354431443
  143. 143. Siegel GJ2006Basic Neurochemistry, molecular, cellular and medical aspects. Burlington: Elsevier. 974 p.
  144. 144. SteckelingsU. M.RompeF.KaschinaE.NamsolleckP.GrzesiakA.Funke-KaiserH.BaderM.UngerT.2010The past, present and future of angiotensin II type 2 receptor stimulation. J Renin Angiotensin Aldosterone Syst, 1116773
  145. 145. SunY.AsnicarM.SmithR. G.2007Central and peripheral roles of ghrelin on glucose homeostasis. Neuroendocrinology, 86321528
  146. 146. SundlerF.AlumentsJ.HakansonR.IngemanssonS.FahrenkrugJ.Schaffalitzky deMuckadell. O. B.1977VIP innervation of the gallbladder. Gastroenterology, 7213751377
  147. 147. SwaabD. F.NijveldtF.PoolC. W.1975Distribution of oxytocin and vasopressin in the rat supraoptic and paraventricular nucleus. J Endocrinol, 67461462
  148. 148. SzigetiG. P.SomogyiG. T.CsernochL.SzéllE. A.2005Age-dependence of the spontaneous activity of the rat urinary bladder. J Muscle Res Cell Motil, 2612329
  149. 149. TackJ.DepoortereI.BisschopsR.DelporteC.CoulieB.MeulemansA.JanssensJ.PeetersT.2006Infulence of ghrelin on interdigestive gastrointestinal motility in humans. Gut, 5532733
  150. 150. TanabeN.UenoA.TsujimotoG.1993Angiotensin II receptors in the rat urinary bladder smooth muscle: type 1 subtype receptors mediate contractile responses. J Urol, 150310561059
  151. 151. TanakaH.HommaK.WhiteH.YanagidaT.IkebeM.2008Smooth Muscle Myosin Phosphorylated at Single Head. J Biol Chem, 283231561115618
  152. 152. Tena-SempereM.2008Ghrelin and reproduction: ghrelin as novel regulator of the gonadotropic axis. Vitam. Horm, 77285300
  153. 153. ThibonnierM.PrestonJ. A.DulinN.WilkinsP. L.Berti-MatteraL. N.MatteraR.1997The human 3pituitary vasopressin receptor: ligand binding profile and density-dependent signaling pathways. Endocrinology, 138: 4109 EOF22 EOF
  154. 154. ThibonnierM.1 EOF11 EOF1992Signal transduction of 1-vascularvasopressin receptors. Regul Pept, 38: 1-11
  155. 155. TobinV. A.HashimotoH.WackerD. W.TakayanagiY.LangnaeseK.CaquineauC.NoackJ.LandgrafR.OnakaT.LengG.MeddleS. L.EngelmannM.LudwigM.2010An intrinsic vasopressin system in the olfactory bulb is involved in social recognition. Nature, 464413417
  156. 156. Tolekova AN, Hadzhibozheva PV, Iliev RN, Georgiev TsK, Trifonova KY, Sandeva RV, Kalfin RE, Ilieva GS2010Participation of extracellular Ca2+) or ghrelin in peptide-mediated contraction of strips from rat urinary bladder. Regul Pept,162(1-3): 79 EOF83 EOF
  157. 157. TouyzR. M.BerryC.2002Recent advances in angiotensin II signaling. Brazilian J Med Biol Res, 35: 1001−1015.
  158. 158. UrataH.KinoshitaA.MisonoK. S.BumpusF. M.HusainA.1990Identification of a highly specific chymase as the major angiotensin II-forming enzyme in the human heart. J Biol Chem, 2652234822357
  159. 159. UveliusB.GabellaG.1998The distribution of intramural nerves in urinary bladder after partial denervation in the female rat. Urol Res, 26291297
  160. 160. UveliusB.LundinS.AnderssonK. E.1990Content and contractile effect of arginine vasopressin in rat urinary bladder. Eur J Pharmacol, 1823549554
  161. 161. VaccarinoF. J.RankinJ.1989Nucleus accumbens cholecystokinin CCK) can either attenuate or potentiate amphetamine-induced locomotor activity: evidence for rostral-caudal differences in accumbens CCK function. Behav Neurosci, 103831836
  162. 162. Van Der LelyA. J.TschopM.HeimanM. L.GhigoE.2004Biological, Physiological, Pathophysiological, and Pharmacological Aspects of Ghrelin. Endocrine Rev, 253426457
  163. 163. Van Der LelyA. J.TschopM.HeimanM. L.GhigoE.2004Biological, Physiological, Pathophysiological, and Pharmacological Aspects of Ghrelin. Endocrine Rev,253426457
  164. 164. VaragicJ.TraskA. J.JessupJ. A.ChaellM. C.FerrarioC. M.2008New angiotensins. J Mol Med, 866663671
  165. 165. VargiuR.UsaiP.De LisaA.ArgiolasA.ScarpaR. M.GessaG. L.UsaiE.FraschiniM.MancinelliR.2004Vasopressin excitatory action on smooth muscle from human renal calyx and pelvis. Pharmacol Res, 506617622
  166. 166. VartiainenJ.2009Ghrelin, obesity and type 2 diabetes. Genetic, metabolic and epidemiological studies. Acta Univ Oul D, Oulin yliopisto, Oulu university press, Oulu, Finland, 1114
  167. 167. VonBohlen.HalbachO.AlbrechtD.2006The CNS renin-angiotensin system. Cell Tissue Res.,326599616
  168. 168. WaldeckK.LindbergB. F.PerssonK.AnderssonK. E.1997Characterization of angiotensin II formation in human isolated bladder by selective inhibitors of ACE and human chymase: a functional and biochemical study. Br J Pharmacol, 121610811086
  169. 169. WangG. D.WangX. Y.HuH. Z.FangX. C.LiuS.GaoN.XiaY.JDWood2005Angiotensin receptors and actions in guinea pig enteric nervous system. Am J Physiol Gastrointest Liver Physiol, 289(3): G61426
  170. 170. WatanabeT.BarkerT.BerkB.2005Angiotensin II and the Endothelium: Diverse Signals and Effects. Hypertension, 45163169
  171. 171. Weaver-OsterholtzD.ReamsG.WuZ.KnausJ.CampbellF.BauerJ. H.1996The urinary bladder angiotensin system: response to infusions of angiotensin I and angiotensin-converting enzyme inhibitors. Am J Kidney Dis, 284603609
  172. 172. Wiley KE, Davenport AP2002Comparioson of vasodilators in human internal mammary artery: ghrelin is a potent physiological antagonist of endothelin-1. Br J Pharmacol, 136811461152
  173. 173. XuD.YuB. P.LuoH. S.ChenL. D.2008Control of gallbladder contractions by cholecystokinin through cholecystokinin-A receptors on gallbladder interstitial cells of Cajal. World J Gastroenterol 141828822887
  174. 174. YamadaS.TakeuchiC.OyunzulL.ItoY.2009Bladder angiotensin-II receptors: characterization and alteration in bladder outlet obstruction. Eur Urol, 552482489
  175. 175. YankovK.System Identification оf Biological Processes. Proc. 20th Int.Conf. "Systems for Automation of Engineering and Research SAER-2006Varna, Bulgaria, 144-149.
  176. 176. YankovK.2009Recognition and function association of experimental data. Proc. of the Int. Conference on Information Technologies InfoTech-2009, Varna, Bulgaria, 131141
  177. 177. YankovK.2010Preprocessing of Experimental Data in Korelia Software. Trakia Journal of Sciences, 83): 41-48.
  178. 178. YankovK.2011Evaluation of characteristic parameters of dynamic models. Proceedings of the International Conference on Information Technologies InfoTech-2011,15th- 17 September 2011, Bulgaria,
  179. 179. YannielliP.MolyneuxP.HarringtonM.GolombekD.2007Ghrelin Effects on the Circadian System of Mice. The Journal of Neuroscience, 271128902895
  180. 180. ZelenaD.MerglZ.MakaraG. B.2006The role of vasopressin in diabetes mellitus-induced hypothalamo-pituitary-adrenal axis activation: studies in Brattleboro rats.Brain Res Bull.,6914856
  181. 181. ZetlerG.1983Neuroleptic-like effects of ceruletide and cholecystokinin octapeptide: interactions with apomorphine, methyphenidate and picrotoxin. Eur J Pharmacol 94261270
  182. 182. ZhangJ.RitterR. C.2012Circulating GLP-1 and CCK-8 reduce food intake by capsaicin-insensitive, nonvagal mechanisms. Am J Physiol Regul Integr Comp Physiol 302(2): R264R273.

Written By

Anna Tolekova, Petya Hadzhibozheva, Tsvetelin Georgiev, Stanislava Mihailova, Galina Ilieva, Maya Gulubova, Eleonora Leventieva-Necheva, Kiril Milenov and Reni Kalfin

Published: 19 September 2012