The effect of duodenal distension (DD40) on the ruminal motility (inhibition in % 5 min−1 in comparison to the control values) [10] and behavioral symptoms (number·5 min−1) in sheep before and after voltage-gated calcium channels inhibitor pretreatment at a dose of 1 or 2 mg
Abstract
The significant role of voltage-gated calcium channel (VGCC) L-type antagonists used concomitantly with opioids in attenuation of clinical pain has been confirmed. The aim of this study is to evaluate the comparable effect of intracerebroventricularly (i.c.v.) administered diltiazem, nifedipine and/or verapamil – specific antagonists of VGCCs – in the dose of 1.0 and 2.0 mg in toto on behavioral signs, clinical symptoms, rumen motor activity and biochemical (plasma cortisol and catecholamine—CA) parameters in sheep that have undergone experimental duodenal distension (DD) and to determine whether voltage-gated calcium channel inhibitors (VGCCIs) exert any anti-nociceptive effects under these conditions. The study was carried out using 24 mature, behind reproductive season crossbred ewes, each weighing 32–42 kg. DD was managed by inclusion and the distension of stretching balloon (having 40 mL of water 39°C temperature—DD40). After 5 min of DD40, the signs were observed: an important augmentation of behavioral nociceptive signs, particularly looking around, defecation, head movement, stretching, grinding, lying down, tachycardia, hyperventilation, inhibition of ruminal contractions (70% approximately, during 15 min) and an increase in plasma catecholamine concentration (over sevenfold increase of epinephrine (E): from 0.24 ± 0.12 in control to 2.98 ± 0.21 mM L−1 during 2 h following DD, 2-times norepinephrine (NE): from 1.29 ± 0.23 in control to 2.51 ± 0.30 mM L−1 and 124% increase of dopamine (DA): from 0.94 ± 0.02 in control to 2.10 ± 0.35 mM L−1). VGCCI infusion administered 10 min before duodenal distension diminished severity of jejunal nociceptive reactions, for instance, behavioral symptoms, cardiac acceleration, increase in the number of respiration, inhibition of the reticulum and rumen hypomotility, and effortlessly abolished the increasing presence of plasma cortisol and biogenic amines (CA) release. We suggest that the increase and insistence of visceral hyperalgesia stimulate the flow of Ca2+ ion flow, provoking neurohormones/neuromediators liberatione and cytoplasmic membrane responsiveness modulation. This result confirmed analgesic effects of VGCCIs L- and/or R-type (nimodipine, lercanidipine, SNX-482) obtained by other authors and also suggests that these channels play a crucial role in the modulation of acute visceral hyperalgesia in sheep and may be a therapeutic target for new drugs.
Keywords
- duodenal distension
- diltiazem
- nifedipine
- verapamil
- behavioral signs
- clinical symptoms
- rumen motility
- blood plasma cortisol
- catecholamine concentration
- sheep
1. Introduction
A calcium channel is an ion channel which displays selective permeability to calcium ion (Ca2+). It is sometimes synonymous as voltage-dependent calcium channel (VDCC) [1], although there are also ligand-gated calcium channels (LGCCs) [2]. Voltage-gated calcium channels (VGCCs) are found in excitable cells (e.g., glial cells, muscle, neurons, etc.) [3–6]. There are at least six classes of VGCCs (L-, N-, P/Q-, R- and the T-type channels) that are distributed according to cell type and location, and that may be distinguished by electrophysiological, pharmacological, and structural characteristics. No small organic ligands are clinically available for other than the L-type channels, although there are a number of experimental compounds for the T- and N-type channels [7].
It is known that VGCCs exert a regulatory control of CNS, cardiac, and muscularly activities and that their activity disorders can provide raise to physiopathological cases extending from cardiac and vascular disorders to central nervous system pathologies. Voltage-gated calcium channels inhibitors (VGCCIs) have been applied profitably to treat epilepsy and are arising as probable curative pathways as long as pathology, such as algesia, Parkinson’s disease, anxiety, and addiction [8]. Therefore, calcium channels can be drug targets for nervous system diseases, and potential challenges and opportunities for the development of new clinically effective calcium channel inhibitors [8].
L-type VGCCs are located in neuronal cells, dendrites, spinal cord, adrenal gland, skeletal cardiac and smooth muscles, and many other locations [9–14]. L-type calcium currents typically require strong depolarization for their activation and are blocked by different antagonists (VGCCIs) including dihydropyridines (nifedipine), benzothiazepines (diltiazem), and phenylalkylamines (e.g., verapamil). VGCCIs are a class of drugs that disrupts the movement of calcium ions through calcium channels. These substances, by relaxing the smooth muscle tone, are commonly used to treat high blood pressure (hypertension), migraines,
The mode of action of verapamil similarly to diltiazem and nifedipine, is based on binding with the largest subunit α1 of Ca2+ channels. This subunit incorporates the conduction pore, voltage sensor, gating apparatus, and several regulation sites, e.g., by second messengers, drugs, and toxins. VGCCIs inhibit Ca2+ ions influx to the cells, which are the main Ca2+ currents in muscle and endocrine cells initiating many activities, such as gene expression, muscle contraction (excitation-contraction coupling), hormone secretion, neurotransmitter release, cell growth and regulation, neurons migration, cell damage, and death or finally cell survival [17].
Acute intestinal distension (“colic”), similarly as functional gastrointestinal disorders, inflammatory bowel disease or irritable bowel syndrome causes visceral hypersensitivity and may produce persistent pain [17, 18]. Visceral pain is described as pressure-like, intermittently squeezing or cramp, not well localized, vague in character, and difficult for patients to describe [19]. Visceral pain is frequently accompanied by nausea, sweating, defecation, vocalization, grinding, head movement, hyperventilation, hypertension, tachycardia, hypercortisolemia, and hypercatecholaminemia (Table 1).
Accompanying symptoms | 0–5 | 5–10 | 10–15 | 25–30 | 55–60 | 120 min | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
DD | 1 | 2 | 3 | DD | 1 | 2 | 3 | DD | 1 | 2 | 3 | DD | 1 | 2 | 3 | DD | 1 | 2 | 3 | DD | 1 | 2 | 3 | |
Inhibition ruminal activity | 4+ | − | + | − | 4+ | − | ± | − | 3+ | 2 | + | + | − | − | − | − | − | − | ± | − | − | − | − | − |
Looking around | 3+ | ± | ± | ± | 2+ | ± | ± | ± | + | + | + | + | − | − | − | + | − | − | − | − | − | − | − | − |
Defecation | 3+ | − | − | − | + | − | ± | − | − | ± | − | ± | − | − | ± | + | − | − | − | − | − | − | − | − |
Head movements | 3+ | − | − | − | 2+ | ± | ± | ± | − | − | − | − | − | − | ± | + | − | − | − | − | − | − | ± | − |
Stretching | 2+ | − | − | − | − | + | − | − | − | − | + | ± | − | − | − | − | − | − | − | − | − | − | − | − |
Grinding | 2+ | ± | ± | ± | ± | − | + | + | − | ± | ± | ± | − | − | − | − | − | − | − | − | − | − | − | − |
Lying down | 2+ | − | − | − | − | + | − | − | − | ± | ± | − | − | − | − | − | − | − | − | − | − | − | − | − |
Bleating | + | − | − | − | − | + | − | − | − | − | − | − | − | + | + | + | + | − | − | − | − | − | − | − |
Tachycardia | 4+ | ± | 3+ | 3+ | ± | 4+ | − | ± | 4+ | − | 3+ | ± | 3+ | − | ± | ± | 3+ | − | ± | ± | 3+ | − | − | − |
Hyperventilation | 4+ | ± | − | ± | 3+ | − | − | ± | 4+ | − | − | ± | 3+ | − | − | − | 3+ | − | − | − | 3+ | − | − | − |
Gastrointestinal sensory system consist intrinsic (enteric) sensory afferents and extrinsic (vagus, spinal cord, pelvic) afferents. Intrinsic sensory system functions independently of the CNS. Enterochromaffin cells within mucosa and enteroendocrine cells release 5-HT, CCK, orexin, and leptin which modulates and regulates motor activity of intestine [20, 21]. The submucosal enteric plexus and myenteric plexus have a high degree of synaptic interactions (enteric nervous system or a “gut brain”), which can be either inhibitory or stimulatory for the purpose of regulating gastrointestinal motility and peristalsis [22, 23].
Mechanisms of the reception, transduction, transformation and modulation of nociceptive stimulus, and reaction diminishing response on nociception are regulated by afferent systems to CNS and efferent systems from CNS “stimulating” reaction, but quenching (pain-gated).
Several data show antinociceptive/antistressoric effects of organic Ca2+ inhibitors of L-VGCCs in acute duodenal pain of sheep [16, 20]. These inhibitors potentiate the analgesic action of κ-opioidergic receptor agonists [15], as well as morphine by decreasing opioids’ tolerance [24]. It was also shown by Bongianni et al. [25] that VGCCIs suppress not only metabolic but also behavioral expression of the morphine withdrawal syndrome. In experiments performed on mice, it was shown that verapamil blocked amphetamine and also physostigmine induced footshock-induced aggression [26]. It was postulated by Michaluk et al. [27] that VGCCIs show antinociceptive properties; but they also change the territorial behavior of animals [28] and conspecific aggression in fish [29]. Such effects were probably caused by the inhibition of Ca2+ entry into neurons, preventing the appearance of synaptic vesicles in axon terminal, and release of neurotransmitter into the synaptic cleft. Davis and Bauer [14] have shown in experiments performed on rats, that activation of L-VGCCs are necessary for the long-term retention of fear excitation.
A duodenal and/or colonic distension method, provoking jejunal pain, stimulates hypothalamic-pituitary-adrenal-cortical (HPA) and sympatico-adrenal system (SAS), pathways that revealed as an increase in cortisol and CA in blood plasma [18, 20]. A different role of L-type antagonists for VGCC has been previously identified in different types of experimental and clinical pain in man and animals. Present study examined comparative role of VGCC blockers from different chemical groups—diltiazem, nifedipine, and verapamil administered
2. Material and methods
2.1. Preparation of animals
Experiment was carried out on 24 mature crossbred ewes, Polish merino sheep weighing 32–42 kg B.W., being
Investigations were performed in four steps (groups, each of six animals for every drug). Every exercise was carried together on two unfed animals, placed in separate boxes at seven days interruption. Blood collection was performed 30 min prior to investigation, in 0 time and 5, 10, 15, 30, 60, and 120 min (Figure 1).
In the first experimental group, a 60 min recording of the ruminal motility was performed in each animals (n = 6) receiving 100 μL of 20% DMSO (control for nifedipine) or 0.9% NaCl (control for diltiazem and/or verapamil), during 1 min infusion (20 min after the 1st venous blood collection) into the lateral ventricle of the brain (
The second group of sheep (n = 6) were subjected to VGCCIs treatment alone, after 60 min control recording of rumen motility. Every animal received each dose of the substance (with 7 days interval). After the second collection of the venous blood, the sheep were
In the third group of sheep (n = 6), after 30 min of control registration of the rumen motility, a rubber balloon (10 cm long) was inserted into the duodenum
In the fourth group of sheep (n = 6), after 30 min of control registration of the rumen motility, a rubber balloon (10 cm long) was inserted into the duodenum and 30 min after the animals received the 100 μL
Experimental procedure lasted for 10 months. The doses of 1.0 and 2.0 mg diltiazem, nifedipine or verapamil
2.2. Mechanography
The ruminal contractions were analyzed using the electronic tensometric recorder PIT 212 (COMT, Bialystok, Poland). The analysis of mechanograms and calculations of results were performed similarly as in a case of electromyographic recording [32]. The number of the rumen motor activity was determined by the frequency on mechanograms, with 5 min intervals before and after the DD40.
2.3. The estimation of blood cortisol and catecholamine (CA) levels
Blood samples for the analysis of CA estimation were collected from the jugular external vein (according to a scheme described above—Figure 1). Blood samples were placed in 10 mL test tubes containing reduced glutathione (0.05 mM). The plastic tubes were maintained on ice, and after the centrifugation, plasma was stored at −80°C, until the beginning of the analytical process. The detection of CA levels was performed by radioimmunoassay using REA kits (CATECHOLA, Czech Republic). The sensitivity of this method was for E, 0.37, for NE, 0.53, and for DA, 0.85 nM L−1. The intra serial error for E was of 3%, for NE 4.2%, and for DA 6.1%, whereas the error among the series was of 4.2, 7.4, and 6.6%, respectively.
Cortisol levels were detected by radioimmunoassay (RIA), according to previous experiments [18]. The mean intra and inter assay of the method was of 9.5 pg, for a sample of 10 μL (ORION DIAGNOSTICA, Espoo). Δmax concentration for each hormone was the difference between the basal concentration and the highest concentration measured.
2.4. The determination of cardiac and ventilation rates
The heart and respiratory rates were measured by determining the number of heart frequencies, as well as by observing the respiratory thoracic movements, using the stethoscope for 1 min. These estimations were detected out by the same person prior to blood test for analysis, according to earlier article [20].
The lack of effect of solvents was determined in preliminary experiments [29, 32].
2.5. Statistical analysis
Statistical significance of the results was carried out through the comparison of control values with those obtained after mechanical distension (duodenal distension—DD40), as well as after VGCCIs premedication and concurrent DD40, using a multifactorial analysis of variance (ANOVA). The statistical significance of the results was detected with a post hoc Tukey-Kramer test; the results are shown as a mean ± SEM. A p value, less than 0.05 was considered statistically significant in all tests.
The researches were performed according to the rules of the Principles of Laboratory Animal Care (NIH publication no. 86-23, revised 1985), as well as the specific national laws on protection of animal (National Law for Animals Protection – 1997, Dz. U.23 XI; Permission of 3rd Local Ethical Commission No. 9/2001 issued 11.01.2001).
3. Results
The influence of DD on behavioral signs, clinical symptoms, reticulo-ruminal contraction and blood plasma cortisol, and CA level was investigated. Before the physiological experimentation, no alteration was observed neither in the physiological behavior of two animals, simultaneously tested in individual cages, nor in the motoric and behavioral response to environmental factors. The mean cardiac frequency was 75.2 (±5.11) and the number of breathing was 35.6·min−1 (±4.21), and the reticulo-ruminal frequency was 6.45 ± 0.75 c × 5 min−1 in 30 min, before DD. After the implantation of an empty rubber balloon into the duodenum, the observed changes were NS in animal behavior or in the heart beat (70.5 beats·min−1 (±8.2)), respiration frequency (42.1 ± 6.35·min−1, Table 1) and reticulo-ruminal contractions (6.12 ± 0.28 c·5 min−1). Five-minute duodenal distension induced highly statistically significant alterations in the behavioral signs of animals [10].
3.1. The effect of DD on the behavioral and clinical symptoms, blood plasma cortisol,
and/or catecholamine level
Duodenal distension by 40 mL of warm water resulted in a significant increase in the behavioral pain responses: motility, bleating, teeth grinding, prostration, wetting, defecation, tachycardia (from 60 ± 3 beats·min−1 to 86 ± 6.2 beats·min−1), hyperventilation (from 36.3 ± 3.6 number·min−1 to 50.3 ± 4.5 number·min−1), inhibition of reticulo-rumen contractions rate (from 6.15 ± 0.54 c × 5 min−1 in control to 1.09 ± 0.33 c × 5 min−1 during DD and to 1.35 ± 0.52 c × 5 min−1 10 min after DD (Figure 2; p = 0.001), from −82.2% to −78.0% during 15–20 min; a significant increase in plasma cortisol concentration from 10.51 ± 2.66 ng·mL−1 in control to 24.72 ± 8.25 ng·mL−1 during DD and to 34.44 ± 5.46 ng·mL−1 (p ≤ 0.01) 10 min after DD (Figure 3); a statistically significant increase of plasma catecholamine concentration (over seven-fold increase of E from 0.34 ± 0.12 nM·L−1 in control to 2.87 ± 0.65 nM L−1, during 2 hours following the DD (Figure 4); 100% NE—from 1.29 ± 0.23 nM·L−1 in control to 2.32 ± 0.24 nM·L−1—120 min after DD (Figure 4) and 126% increase of DA from 0.93 ± 0.02 nM L−1 in the control to 2.33 ± 1.16 nM L−1, 120 min after DD) (Figure 4).
3.2. The influence of VGCCIs premedication on the behavioral changes, clinical symptoms, rumen motility, plasma cortisol, and catecholamine level in animals with/without DD
VGCCIs premedication caused that inhibition of rumen frequency after 5 min DD, decreasing from average 6.12 ± 0.40 to 5.00 ± 0.61, in 5 min, and 4.00 ± 0.38 c × 5min−1, in 10 min, after DD, but not from 6.15 ± 0.54 in control to 1.09 ± 0.33 c × 5 min−1 after DD (Table 2, Figure 2). Plasma cortisol concentration changed from 10.83 ± 1.19 in control to 11.95 ± 1.25, during (NS), and 9.53 ± 1.36 (NS) 30 min, after DD, but not increased from 10.51 ± 2.66 in control to 24.72 ± 8.25, during DD, and 34.44 ± 5.46 (+227.7%) 10 min, after DD (p˂0.001, Figure 3). Diltiazem premedication caused that increase of plasma CA concentration after 5 min DD, decreased E from average +606.41% in control to +23.02%, during 120 min after DD (Figure 4); NE from +120.95% in control to −21%, during 120 min after DD (Figure 5) and DA from +124.2% in control to −24,8%, during 120 min after diltiazem premedication (Figure 6).
Drugs | Control | 5 min | 10 min | 15 min | 20 min | 25 min | 30 min |
---|---|---|---|---|---|---|---|
0.9% NaCl | 6.45 ± 0.75 | 6.12 ± 0.28 | 6.00 ± 0.25 | 6.80 ± 0.33 | 6.10 ± 0.60 | 6.35 ± 0.15 | 6.11 ± 0.43 |
DD40 | 6.15 ± 0.54 | 1.09 ± 0.33* | 1.78 ± 0.49* | 1.35 ± 0.52* | 2.20 ± 0.31* | 0.61 ± 0.12* | 4.91 ± 0.75 |
Diltiazem + DD40 | 5.00 ± 0.61* | 4.00 ± 0.38* | 3.80 ± 0.60* | 4.23 ± 0.36* | 5.14 ± 0.42 | 4.82 ± 0.64 | 6.12 ± 0.40 |
Nifedipine + DD40 | 5.82 ± 0.45 | 1.89 ± 0.81* | 5.54 ± 0.23 | 4.88 ± 0.62 | 5.12 ± 0.74 | 6.11 ± 1.11 | 5.59 ± 1.22 |
Verapamil + DD40 | 6.12 ± 0.89 | 5.33 ± 0.51 | 5.75 ± 0.11 | 5.05 ± 0.80 | 4.97 ± 0.65 | 5.55 ± 1.02 | 5.85 ± 0.61 |
Nifedipine
Verapamil
Control | 5 min | 10 min | 20 min | 30 min | 60 min | 120 min | |
---|---|---|---|---|---|---|---|
0.9% NaCl | 11.35 ± 2.40 | 11.50 ± 2.61 | 11.05 ± 2.58 | 10.17 ± 6.71 | 12.01 ± 1.86 | 9.87 ± 0.25 | 10.02 ± 2.02 |
DD40 | 10.51 ± 2.66 | 24.72 ± 8.25* | 34.44 ± 5.46* | 31.52 ± 2.91* | 29.65 ± 4.61* | 23.10 ± 1.61* | 16.16 ± 2.56* |
Diltiazem + DD40 | 10.83 ± 1.19 | 11.95 ± 1.25 | 9.58 ± 1.81 | 8.52 ± 1.13 | 9.53 ± 1.36 | 10.99 ± 1.68 | 9.8 ± 2.31 |
Nifedipine + DD40 | 11.81 ± 1.13 | 10.25 ± 1.51 | 10.25 ± 1.17 | 11.94 ± 1.65 | 12.25 ± 1.39 | 15.75 ± 1.69 | 11.85 ± 1.35 |
Verapamil + DD40 | 11.53 ± 0.98 | 7.91 ± 1.58* | 10.83 ± 1.17 | 14.63 ± 1.53 | 13.53 ± 1.58 | 10.49 ± 1.69 | 10.96 ± 1.36 |
Verapamil
Verapamil
Catecholamine | Time (in min) | ||||||
---|---|---|---|---|---|---|---|
0 | 5 | 10 | 15 | 30 | 60 | 120 | |
0.9% NaCl (100 μL) | 0.98 ± 0.00 | 0.75 ± 0.00 | 0.82 ± 0.00 | 0.71 ± 0.00 | 0.85 ± 0.11 | 0.85 ± 0.00 | 0.99 ± 0.12 |
DD40 | 0.34 ± 0.12 | 2.42 ± 0.09 | 3.15 ± 0.68 | 3.45 ± 0.53 | 3.38 ± 1.82 | 2.58 ± 1.13 | 2.87 ± 0.65 |
Diltiazem + DD40 | 0.70 ± 0.12 | 0.98 ± 0.42 | 0.99 ± 0.25 | 0.88 ± 0.10 | 1.01 ± 0.20 | 0.88 ± 0.12 | 0.56 ± 0.23 |
Nifedipine + DD40 | 0.90 ± 0.12 | 0.97 ± 0.14 | 0.89 ± 0.25 | 1.31 ± 0.58 | 1.41 ± 0.38 | 0.99 ± 0.18 | 0.90 ± 0.41 |
Verapamil + DD40 | 1.19 ± 0.29 | 1.34 ± 0.31 | 1.30 ± 0.28 | 1.34 ± 0.26 | 1.24 ± 0.59 | 1.39 ± 0.21 | 1.58 ± 0.35 |
0.9% NaCl (100 μL) | 1.30 ± 0.16 | 1.32 ± 0.15 | 1.37 ± 0.48 | 1.36 ± 0.19 | 1.33 ± 0.58 | 1.33 ± 0.44 | 1.28 ± 0.17 |
DD40 | 1.29 ± 0.23 | 2.85 ± 0.48 | 2.93 ± 0.51 | 2.94 ± 0.76 | 2.31 ± 0.30 | 2.11 ± 0.32 | 2.32 ± 0.24 |
Diltiazem + DD40 | 0.82 ± 0.20 | 0.61 ± 0.31 | 0.83 ± 0.13 | 0.83 ± 0.33 | 1.12 ± 0.33 | 0.89 ± 0.12 | 0.69 ± 0.04 |
Nifedipine + DD40 | 0.95 ± 0.06 | 1.01 ± 0.14 | 0.99 ± 0.28 | 1.12 ± 0.38 | 1.41 ± 1.22 | 1.12 ± 0.72 | 1.43 ± 1.23 |
Verapamil + DD40 | 1.29 ± 0.22 | 1.94 ± 0.66 | 1.52 ± 0.42 | 1.63 ± 1.12 | 1.68 ± 1.10 | 1.42 ± 0.48 | 1.32 ± 0.24 |
0.9% NaCl (100 μL) | 1.23 ± 0.08 | 1.24 ± 0.06 | 1.26 ± 0.10 | 1.24 ± 0.09 | 1.25 ± 0.12 | 1.31 ± 0.01 | 1.15 ± 0.07 |
DD40 | 0.93 ± 0.02 | 1.26 ± 0.01 | 2.18 ± 0.30 | 2.51 ± 0.52 | 2.25 ± 0.52 | 2.10 ± 0.35 | 2.33 ± 1.16 |
Diltiazem + DD40 | 0.99 ± 0.09 | 0.75 ± 0.51 | 0.53 ± 0.18 | 1.05 ± 0.26 | 0.98 ± 0.25 | 0.86 ± 0.53 | 0.74 ± 0.19 |
Nifedipine + DD40 | 0.96 ± 0.02 | 1.29 ± 0.12 | 1.53 ± 0.42 | 1.62 ± 0.28 | 2.52 ± 1.41 | 1.32 ± 0.19 | 1.02 ± 0.32 |
Verapamil + DD40 | 0.92 ± 0.04 | 1.51 ± 0.12 | 1.63 ± 0.09 | 1.51 ± 0.08 | 1.50 ± 0.12 | 1.53 ± 0.13 | 1.48 ± 0.25 |
4. Discussion
The results of this experiment showed that 1 min diltiazem, nifedipine, and/or verapamil (VGCCIs)
In our study, saline and 20% DMSO
It is known that DD40 provoked stimulation of behavioral signs, clinical symptoms, and statistically significant increase in plasma cortisol and catecholamine concentrations (Table 1, Figures 3–6).
Five-minute DD episode increased the plasma cortisol concentration average for 153% during 120 min after DD, in comparison to the control values. Ten-minute VGCCIs premedication diminished the plasma cortisol release by an average of 139.5 % (diltiazem), and 141% (nifedipine and verapamil) (p ≤ 0.001; Table 3, Figure 3) respectively.
Five-minute DD episode increased the plasma catecholamine concentration average: E 768%, NE 98.5%, and DA 124% during 120 min after DD. Diltiazem, nifedipine, and verapamil minimized the increase of plasma catecholamine concentration, which was caused by visceral pain, provoked by duodenal distension. Average of catecholamine release inhibition by VGCCIs were for E—773.3%, NA—90%, and DA—90.2%, during 120 after 5 min DD episode (p ≤ 0.001; Table 4, Figures 4–6). The most anticatecholaminergic activity was detected for diltiazem. In our study, we found that all the VGCCIs—whatever their chemical origin—in premedication attenuated vegetative signs and clinical symptoms, HPA and SAS stimulation axes caused by acute 5 min duration nocifensive factor (duodenal distension) in sheep.
This confirms the results obtained by Qian et al. [17] that Cav1.2 and Cav2.3 channels in colonic primary sensory neurons play an important role in visceral inflammatory hyperalgesia, which may be a potential therapeutic target, because L-type and R-type selective colonic channel blockers may block calcium currents which are importantly increased in colonic dorsal root ganglion (DRG) neurons of 2,4,6-trinitrobenzenesulfonic acid-treated rats in comparison with control animals. The author cited above concluded that L-type channel antagonist (nimodipine) and R-type channel antagonist (SNX-482) attenuates visceral pain in 2,4,6-trinitrobenzenesulfonic acid intrathecal injected. The results obtained confirm the hypothesis that L-type and/or R-type calcium channels play a more crucial role in pathology of visceral pain in animals.
A moderate degree of mechanical duodenal distension (DD20 and DD30) in sheep reduced the frequency of forestomach and abomasum motor activity by 45 and 52%, respectively [30], whereas, strong distension (DD40 and DD80) provoked the total contraction inhibition in conscious animals accompanied by the acute visceral pain [21, 33]. There is a direct relationship between the viscero-visceral reflex and visceral pain [34]. Visceral pain is a general sign involved in many gastro-duodenal and gastro-colonic disorders, such as colic, inflammatory processes, and other diseases. These symptoms are accompanied by stimulation of the HPA (neuropeptides, hormones, e.g., cortisol) and SAS (catecholamine, 5-HT, neuropeptides) axes and the exacerbation of motivational and motor CNS structures (limbic system) involved in many quinine, neuropeptides, and necrohormones release useful in alarm reactions and defense of animals.
4.1. Other types of calcium channel blockers used in the treatment of pain
Voltage-gated calcium channels are made with subunit α1 which forms a channel pore and subunit α2δ, which facilitates movement to the membrane surface [35]. There are ten different α1δ subtypes and four α2δ. α2δ1 and α2δ2 subtypes bind gabapentin and pregabalin. Subtype 1 exists principally in the intermediate matrix (dentate gyrus, insula, cortex, and amygdala) [36].
Subtypes α2δ1 exhibit expression also in dorsal root ganglia, spinal cord and in the small intestine smooth muscle, together with N-type calcium channels [36]. Subtype 2 is found in the periaqueductal gray matter, spinal cord and as diffused all over CNS, but not in the colon or duodenal smooth muscle [37]. Pregabalin and gabapentin bind with subtypes α2δ in the cytoplasm and prevent calcium channels expression on the plasmatic membranes [38]. Preventing the binding and expression blocks calcium conductance and in consequence substance P (SP), calcitonin gene related peptide (CGRP) and glutamate cannot be released from primary afferent neurons [35, 39]. Prevention of nocifensive neurotrasmitters release by gabapentine and pregabaline occurs only during pathological processes, in which calcium channels are up-regulated and activated [40]. Both pregabaline and gabapentine are central analgesics [39]. Gabapentinoids inhibited visceral hypersensitivity in the experimental animals, as well as irritable bowel syndrome in humans [41]. Smalls doses of gabapentine administered with morphine inhibit
Gabapentenoids not only inhibit central nociceptive transmission, but also enhance the intestine susceptibility to distension, possibly by blockage of α2δ subtypes in the smooth muscle [42, 43].
Other calcium channels can be also involved in the development of visceral hypersensitivity. Stimulation of T-type calcium channels, subtype Cav3.2 on the primary signaling visceral afferents was associated with symptoms similar to the irritable bowel syndrome in the animal model. Behavioral symptoms resolved after the application of T-type calcium channels inhibitor [44]. Afferent transduction from mesentery in the experimental intestinal ischaemia was blocked by nifedipine, an L-type calcium channels inhibitor [45].
5. Conclusion
The results of this investigation indicates, that VGCCIs can be applied effectively in visceral pain modulation of animals and could be paid to the use of this kind of medicine, perhaps in human pain treatment as well.
References
- 1.
Dorland’s M Dictionary. Calcium Channels. 32nd Edition, Elsevier, USA, 2016. - 2.
Striggow F, Ehrlich BE. Ligand gated calcium channels inside an aut. Curr. Opin. Cell. Biol. 1996; 8 : 490–495. - 3.
Catteral WA, Perez-Reyes E, Snutch TP, Striessing J. International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels. Pharmacol. Rev. 2005; 57 : 411–425. - 4.
Yamagake M, Namiki A. Calcium channels – basic aspects of their structure, function and gene encoding; anesthetic action on the channels – a review. Can. J. Anaesth. 2002; 49 : 151–164. - 5.
Rang H, Ritter JM, Flower RJ, Henderson G. How drugs act: cellular aspects – excitation, contraction and secretion. In: Rang & Dale’s Pharmacology. 8th Edition, Elsevier Churchill Livingstone, 2016; pp. 50–65. - 6.
Morgan AJ, Platt FM, Lloyd-Evans E, Galione A. Molecular mechanisms of endolysosomal Ca2+ signaling in health and disease. Biochem. J. 2011; 439 : 349–374. - 7.
McDonough SI. Calcium Channel Pharmacology. Kluwer Academic/Plenum, New York, 2004. - 8.
Zamponi GW. Targeting voltage-gated calcium channels in neurological and psychiatric diseases. Nat. Rev. Drug Discov. 2016; 15 : 19–34. - 9.
Leone M, Franzini A, Proietti Cecchini A, Mea E, Brogi G, Bussone G. Management of chronic cluster headache. Curr. Treat. Options Neurol. 2011; 13 : 56–70. - 10.
Guttierez-Martin Y, Martin-Romero FJ, Henao F. Store-operated calcium entry in differentiated C2C12 skeletal muscle cells. Biochem. Biophys. Acta. 2005; 1711 : 33–40 - 11.
Sicca D. Calcium channel blockers and the kidney. Clin. Cornerstone. 2004; 6 : 39–52. - 12.
Long W, Zhao Y, Zhang L, Longo LD. Role of Ca2+ channels in NE induced increase in [Ca2+](i) and tension in fetal and adult cerebral arteries. Am. J. Physiol. 1999; 277 : R286–R294. - 13.
Yamagishi S, Takeuchi M. Nifedipine inhibits tumor necrosis factor-alpha-induced upregulation of monocyte chemoattractant protein-1 mRNA levels by suppressing CD40 expression in endothelial cells. Drug. Exp. Clin. Res. 2005; 31 : 13–17. - 14.
Davis SE, Bauer EP. L-type voltage-gated calcium channels in basolateral amygdala are necessary for fear extinction. J. Neurosci. 2012; 32 : 13582–13586. - 15.
Leblondel G, Allain P. Ca2+ uptake and energy supply of sheep heart mitochondria in presence of some calcium antagonists. Res. Commun. Chem. Pathol. Pharmacol. 1984; 44 : 499–502. - 16.
Kania BF, Ŝutiak V. Influence of centrally administered diltiazem on behavioral response, clinical symptoms, reticulo-ruminal contraction and plasma catecholamine level after experimentally induced duodenal distension in sheep. Res. Vet. Sci. 2011; 90 : 291–297. - 17.
Qian A, Song D, Li Y, Liu X, Tang D, Yao W, Yuan Y. Role of voltage gated Ca2+ channels in rat visceral hypersensitivity change induced by 2,4,6-trinitrobenzene sulfonic acid. Mol. Pain. 2013; 9 : 15 DOI: 10.1186/1744-8069-9-15 - 18.
Kania BF, Wrońska D. Supraspinal basis of analgesic and clinical effects of the metabotropic glutamate mGluR1 antagonist during colonic distension in sheep. Small Rum. Res. 2014; 117 : 84–93. - 19.
Bielefeldt K, Christianson JA, Davis RM. Basic and clinical aspects of visceral sensation: transmission in the CNS. Neurogastroenterol. Motil. 2005; 17 : 488–499. - 20.
Kania BF, Brytan M, Tomaszewska D. Centrally administered verapamil prevents the autonomic reaction to visceral pain in sheep. Res. Vet. Sci. 2009; 86 : 121–128. - 21.
Brikas P, Kania BF, Fioramonti J, Buéno L. Central and peripheral serotonergic influences on viscerovisceral inhibitory reflex during duodenal distension in sheep. Dig. Dis. Sci. 1993; 38 : 1079–1086. - 22.
Blackshaw LA, Brookes SJ, Grundy D, Scheman M. Sensory transmission in the gastrointestinal tract. Neurogastroenterol. Motil. 2007; 19 : 1–3. - 23.
Ossipov MH, Morimura K, Porreca F. Descending pain modulation and chronification of pain. Curr. Opin. 2014; 8 : 143–151. - 24.
Shimizu N, Kishioka S, Maeda T, Fukazawa Y, Yamamoto C, Ozaki M, Yamamoto H. Role of pharmacokinetic effects in the potentiation of morphine analgesia by L-type calcium channel blockers in mice. J. Pharmacol. Sci. 2004; 94 : 240–245. - 25.
Bongianni F, Carla V, Moroni F, Pellegrini-Giampietro DE. Calcium channel inhibitors suppress the morphine-withdrawal syndrome in rats. Br. J. Pharmacol. 1986; 88 : 561–567. - 26.
Srivastava SK, Nath C. The differential effects of calcium channel blockers in the behavioral despair test in mice. Pharmacol. Res. 2000; 42 : 293–297. - 27.
Michaluk J, Karolewicz B, Antkiewicz-Michaluk L, Vetulani J. Effects of various Ca2+ channel antagonists on blond pressure in the rat. Eur. J. Pharmacol. 1998; 352 : 189–197. - 28.
Kavaliers M. Aggression and defeat-induced opioid analgesia displayed by mice are modified by calcium channel antagonists and agonists. Neurosci. Lett. 1987; 74 : 107–111. - 29.
Kania BF, Dębski B, Wrońska D, Zawadzka E. Verapamil – L-type voltage-gated calcium channel inhibitor diminishes aggressive behavior in male Siamese fighting fish. Pol. J. Vet. Sci. 2015; 18 : 401–406. - 30.
Kania BF, Zaremba-Rutkowska M, Romanowicz K. Experimental intestinal stress induced by duodenal distension in sheep. J. Anim. Feed Sci. 1999; 8 : 233–245. - 31.
Sorraing JM, Fioramonti J, Buéno L. Central and peripheral serotonergic control of forestomach motility in sheep. J. Vet. Pharmacol. Ther. 1985; 8 : 312–319. - 32.
Kania BF, Brikas P, Buéno L, Fioramonti J, Zaremba–Rutkowska M. The evaluation of the role of CCK in the opioid modulation of the motility of the gastrointestinal tract in sheep. J. Vet. Pharmacol. Ther. 1999; 22 : 153–160. - 33.
Gullapalli S, Ramarao P. L-type Ca2+ channel modulation by dihydropyridines potentiates kappa-opioid receptor agonist induced acute analgesia and inhibits development of tolerance in rats. Neuropharmacology. 2002; 42 : 467–475. - 34.
De Ponti F, Azpiroz F, Malagelada JR. Reflex gastric relaxation in response to distension of the duodenum. Am. J. Physiol. 1987; 252 : G595–G601. - 35.
Gale JD, Houghton LA. Alpha 2 delta (α(2)δ) ligands, gabapentin and pregabalin: what is the evidence for potential use of these ligands in irritable bowel syndrome. Front. Pharmacol. 2011; 2 : 28. - 36.
Taylor CP, Garrido R. Immunostaining of rat brain, spinal cord, sensory neurons and skeletal muscle for calcium channel alpha2-delta (α2δ) type 1 protein. Neuroscience. 2008; 155 : 510–521. - 37.
Cole RI., Lechnaer SM, Williams LE. Differential distribution of voltage-gated calcium channel alpha-2 delta (α2δ) subunit mRNA-containing cells in the rat central nervous system and the dorsal root ganglia. J. Comp. Neurol. 2005; 491 : 246–269. - 38.
Mich PM, Horne WA. Alternative splicing of the Ca2+ channel β4 subunit confers specificity for gabapentin inhibition of Cav2.1 trafficking. Mol. Pharmacol. 2008; 74 : 904–912. - 39.
Field MJ, Cox PJ, Stott E. Identification of the α2-δ-1 subunit of voltage-calcium calcium channels as a molecular target for pain mediating the analgesic actions of pregabalin. Proc. Nat. Acad. Sci. USA. 2006; 103 : 17537–17542. - 40.
Dooley DJ, Donovan CM, Pugsley TA. Stimulus-dependent modulation of 3H norepinephrine release from rat neocortical slices by gabapentin and pregabalin. J. Pharm. Exp. Ther. 2000; 295 : 1086–1093. - 41.
Stepanovic-Petrovic RM, Tomic MA, Vuckovic SM. The antinociceptive effects of anticonvulsants in a mouse visceral pain model. Anesth. Analg. 2008; 106 : 1897–1903. - 42.
Lee KJ, Kim JH, Cho SW. Gabapentin reduces rectal mechanosensitivity and increases rectal compliance in patients with diarrhoea-predominant irritable bowel syndrome. Aliment. Pharmacol. Ther. 2005; 22 : 981–988. - 43.
Ravnefjord A, Brusberg M, Larsson H, Lindström E, Martinez V. Effects of pregabalin on visceral pain responses and colonic compliance in rats. Brit. J. Pharmacol. 2008; 155 : 407–416. - 44.
Marger F, Gelot A, Alloui A. T-type calcium channels contribute to colonic hypersensitivity in a rat model of irritable bowel syndrome. Proc. Natl. Acad. Sci. USA. 2011; 108 : 11268–11273. - 45.
Jiang W, Kirkup AJ, Grundy D. Mast cells drive mesenteric afferent signaling during acute intestinal ischemia. J. Physiol. 2011; 589 : 3867–3882.