The gastric mucosa is maintained in an intact state by multiple protective mechanisms including humoral and neuronal factors, in spite of its exposure to acid and other chemical hazards . Capsaicin-sensitive afferent neurons play a central role in neuronal mechanisms taking place in the stomach . These afferent neurons have been shown to regulate various gastric functions such as secretion, mucosal blood flow (GMBF), and motility, and modulate the mucosal integrity of the stomach [2-5]. Vanilloid type 1 receptor (VR1), a nonselective cationic channel, has recently been cloned as the binding site of capsaicin , and more recently, has been identified as a member of the transient receptor potential (TRP) family of ion channels . Although the TRP family is activated by a diverse range of stimuli, including the depletion of intracellular Ca2+stores , the VR1 receptor remains the only channel activated by vanilloids such as capsaicin and is now known as TRPV1 . Capsaicin stimulates these afferent neurons via TRPV1, resulting in the release of calcitonin gene-related peptide (CGRP), the predominant neurotransmitter of spinal afferents in the rat stomach, and thus, exerts a gastroprotective action . CGRP has been shown to induce endothelial cells to release nitric oxide (NO), and this molecule is known to strongly mediate the action of CGRP . Other studies have also demonstrated that activation of the bradykinin B2 receptor caused the opening of TRPV1 and modified the action of capsaicin [10, 11].
The secretion of HCO3- from surface epithelial cells is a protective mechanism in the stomach, with HCO3- working in collaboration with mucus gel, which adheres to the surface of mucosa . We previously reported that capsaicin increased duodenal HCO3- secretion mediated by endogenous prostaglandins (PGs) and NO as well as capsaicin-sensitive afferent neurons [12, 13]. We also demonstrated that PGE2 stimulated HCO3- secretion through EP1 receptors in the stomach and EP3/EP4 receptors in the duodenum [14, 15], while the action of capsaicin in the duodenum required the presence of prostacyclin (PGI2) IP receptors . However, few studies have examined the mechanisms involved in gastric HCO3- secretion in response to capsaicin.
We here described the regulatory mechanism underlying capsaicin-induced gastric HCO3- secretion, in relation to sensory neurons, TRPV1, PGs, NO, and bradykinin B2 receptors, and compared it to that of the acid-induced response. In addition, because we found that responses to capsaicin and acid in the duodenum differed concerning PGI2/IP dependency , we also examined these responses in the stomach using mice lacking EP1, EP3 or IP receptors.
3.1. Stimulation by capsaicin and mucosal acidification of HCO3- secretion in the rat stomach
Capsaicin (0.03~0.3 mg/ml) applied to the chamber for 10 min increased the secretion of HCO3- in a dose-dependent manner, and this effect was significant at a dose of 0.1 mg/ml or greater (Figure 1). The stimulatory effect of capsaicin (0.3 mg/ml) on HCO3- was significantly attenuated by the chemical ablation of capsaicin-sensitive afferent neurons as well as the prior administration of indomethacin (5 mg/kg, s.c.) or L-NAME (20 mg/kg, s.c.) (Figure 2). The action of capsaicin was also potently inhibited by the co-application of capsazepine, the TRPV1 antagonist. However, neither the EP1 antagonist, ONO-8711 (10 m/kg, s.c.) nor the bradykinin B2 antagonist, FR172357 (1 mg/kg, i.v.) had any effect on HCO3- secretion in response to capsaicin.
The secretion of HCO3- was also increased in a concentration-dependent manner when the mucosa was acidified following its exposure to 50~200 mM HCl for 10 min (Figure 3). The response to 200 mM HCl was significantly prevented by indomethacin, L-NAME, ONO-8711, and capsaicin pretreatments (Figure 4). However, acid-induced HCO3- secretion in the stomach was not affected by either capsazepine or FR172357.
3.2. Effect of capsaicin and mucosal acidification on PGE2 and 6-keto PGF1 α levels in the rat stomach
The intragastric application of capsaicin (0.3 mg/ml) for 10 min did not affect the amount of PGE2, but significantly increased that of 6-keto PGF1 α to approximately 2.8-fold that of the control level (data not shown). In contrast, the acidification of the gastric mucosa significantly stimulated the production of PGs and increased PGE2 or 6-keto PGF1 α levels to approximately 2 or 3-fold that of basal levels, respectively.
3.3. Stimulation by PGE2, NOR-3, and bradykinin of HCO3-secretion in the rat stomach
The intravenous administration of PGE2 (1 mg/kg) increased the secretion of HCO3- in the stomach, and this response was equivalent to that induced by capsaicin at 0.3 mg/ml (Figure 5). The NO donor, NOR-3 (3 mg/ml), which was applied topically to the mucosa for 10 min, also increased HCO3- secretion. Neither indomethacin, L-NAME, nor FR172357 significantly affected the increase in HCO3- secretion in response to PGE2 (data not shown). Gastric HCO3- secretion was also stimulated by the i.v. administration of bradykinin (30 µg/kg), reached a maximal value of 160% that of the basal level; however, this effect was less potent than that of capsaicin or acidification and completely disappeared after 1 hr (Figure 6). The stimulatory effect of bradykinin on HCO3- was significantly antagonized by FR172357 and attenuated by the prior administration of indomethacin or L-NAME. In addition, the stimulatory effect of bradykinin was almost completely blocked by the chemical ablation of capsaicin-sensitive afferent neurons, but was not significantly affected by pretreatment with capsazepine.
3.4. Effect of capsaicin on HCO3- secretion in wild-type and IP-receptor knockout mice
We previously demonstrated the importance of PGI2/IP receptors in the HCO3- stimulatory action of capsaicin in the duodenum . Since capsaicin also stimulated HCO3- secretion in the stomach, in an indomethacin-inhibitable manner, we attempted to identify the type of prostanoid receptor involved in capsaicin-induced responses in the stomach using EP1-, EP3-, and IP-receptor knockout mice, in comparison with those induced by mucosal acidification.
The mouse stomach spontaneously secreted HCO3- at a rate of 0.1-0.3 µEq/10 min. Capsaicin (0.3 mg/ml), which was applied to the chamber for 10 min, increased the gastric secretion of HCO3- in wild-type mice, and the same effect was also observed in EP1-or EP3-receptor knockout mice, but was absent in mice lacking IP receptors (Figure 7). HCO3- secretion was also increased in wild-type mice following the exposure of the mucosa to 50 mM HCl for 10 min, and the same response was also observed in EP3 and IP, but not EP1 receptor knockout animals (Figure 8). The response induced by either capsaicin or acidification in wild-type animals was significantly attenuated by the pretreatment with indomethacin.
The gastroduodenal mucosa responds to acidification by significantly increasing the secretion of HCO3-, which, in collaboration with mucus, contributes to the mucosal tolerance of luminal acid . We previously reported that the intraluminal application of capsaicin stimulated the secretion of HCO3- in these tissues by activating capsaicin-sensitive afferent neurons [4, 5, 15, 16]. The present study confirmed that both acid and capsaicin increased HCO3- secretion in the stomach, which was mediated by these afferent neurons, and clearly showed the difference in their modes of action in terms of sensitivity to TRPV1 and prostanoid receptors. Furthermore, we observed the involvement of endogenous PGs and NO in the stimulatory action of capsaicin in the stomach, which was consistent with previous findings in the duodenum .
TRPV1 is a nonselective cation channel that responds to protons as well as capsaicin . The binding sites of capsaicin are located on the intracellular site of the receptor protein , whereas the target of protons is thought to be located on the extracellular surface of the receptor protein . When the TRPV1 antagonist, capsazepine was applied to the mucosa together with capsaicin or acid in the present study, it completely blocked the increase in gastric HCO3- secretion induced by capsaicin, but not acid, in spite of both responses being mediated by capsaicin-sensitive afferent neurons. These results are consistent with our previous findings in the duodenum, in which capsazepine significantly mitigated the response induced by capsaicin, but not mucosal acidification . Akiba et al  reported that acid in the lumen induced a mucosal hyperemic response in the rat duodenum in a capsazepine-sensitive manner, and suggested that luminal acid may be an endogenous ligand for duodenal TRPV1. McIntyre et al  described pharmacological differences between the human and rat TRPV1 and demonstrated that capsazepine blocked the response of human, but not rat TRPV1 to low pH. The reason for these different results between studies currently remains unclear. The results of the present study do not exclude the involvement of TRPV1 in the acid-induced secretion of HCO3-; however, the target site of acid may differ from that of capsaicin, ie., the binding site inhibitable by capsazepine. Alternatively, acid may activate these afferent neurons through acid-sensing ionic channels (ASICs). This proposal has been supported by the recent findings in which the acid-induced duodenal HCO3- response was greater in female than male rats, with the different responses being parallel with the intensity of the expression of ASIC3, and ovariectomy suppressed the expression of ASIC3 in the duodenum and abolished such a gender difference in the HCO3- response .
Endogenous PGs are known to be particularly important in the local regulation of HCO3- secretion in the gastroduodenal mucosa. We previously demonstrated, using subtype-specific EP agonists and antagonists, that PGE2 stimulated the secretion of HCO3- in the duodenum through EP3/EP4 receptors and in the stomach through EP1 receptors [15, 16, 29]. Many previous studies reported that mucosal acidification increased HCO3-secretion in these tissues, with a concomitant rise in mucosal PGE2 levels [12, 13, 16]. Capsaicin also stimulated the secretion of HCO3- in the stomach in an indomethacin-inhibitable manner, which suggested the involvement of endogenous PGs. However, capsaicin was shown to increase PGE2 production in the duodenum, but not in the stomach [13, 30]. Notwithstanding, this agent exhibited various effects in the stomach, such as mucosal protection and hyperemia, mediated by capsaicin-sensitive afferent neurons that also depended on endogenous PGs [4, 5, 31]. We confirmed that the intragastric application of capsaicin significantly enhanced the levels of 6-keto PGF1α, the PGI2 metabolite, which was consistent with the findings reported in the mouse stomach [21, 31]. We previously demonstrated that the gastroprotective effects of capsaicin against HCl/ethanol were significantly attenuated by indomethacin in wild-type mice, but were completely absent in animals lacking IP receptors . In the present study, capsaicin increased gastric HCO3- secretion in EP1-and EP3-receptor knockout mice, similar to wild-type mice, but did not in animals lacking IP receptors. These results strongly suggest that endogenous PGI2 plays a supportive role in the action of capsaicin in the stomach, possibly by sensitizing sensory neurons through IP receptors.
However, HCO3- secretion induced by acidification remained unchanged in IP receptor knockout mice and was absent in animals lacking EP1 receptors. These results further support the response of HCO3- induced in the stomach by acidification and capsaicin, but depending on sensory neurons, being mediated by different mechanisms related to PG dependency; the former is mainly mediated by PGE2 through EP1 receptors, while the latter depends on PGI2/IP receptors. Similar results were obtained for the gastric hyperemic response induced by acid or capsaicin . Although gastric hyperemic responses to these treatments were mitigated by the capsaicin pretreatment [2, 32], the response induced by acid required the presence of EP1 receptors , while that evoked by capsaicin required the presence of IP receptors . Thus, it is not unreasonable to assume that the presence of different prostanoid receptors may be required for gastric HCO3-secretion in response to acid or capsaicin.
We found that capsaicin had no effect on the production of PGE2, but significantly increased that of PGI2 in the stomach. Capsaicin-sensitive afferent neurons are known to be abundantly at peri-vascular sites, and the stimulation by capsaicin releases CGRP/NO, resulting in an increase in mucosal blood flow . Harada et al.  reported that the activation of these afferent neurons ameliorated ischemia/reperfusion-induced liver injury by limiting the inflammatory response through an enhancement in endothelial PGI2 production, and suggested that the CGRP-induced activation of both endothelial NO synthase and cyclooxygenase-1 may be involved in this mechanism. Thus, it is possible that capsaicin increases endothelial PGI2 production locally in the stomach when applied topically to the mucosa. The reason why capsaicin had different effects on the production of PGE2 and PGI2 in the stomach currently remains unknown.
The present study also showed that capsaicin-induced HCO3- secretion in the stomach was significantly attenuated by L-NAME, which suggesed the involvement of endogenous NO in this process, in addition to PGs. Several studies showed that CGRP, the dominant neurotransmitter of spinal afferents, had various pharmacological actions, such as vasodilation, that were mediated by endogenous NO [2, 3, 35]. We demonstrated that the NO donor, NOR-3 stimulated gastric HCO3- secretion in the present study, and this was consistent with our previous findings in the duodenum . Nishihara et al  reported that capsaicin increased the release of CGRP and NO in the rat stomach. Although we did not measure NO release in the stomach following the capsaicin treatment, it is assumed that capsaicin activated primary afferent neurons, with the assistance of PGI2, to liberate CGRP, which in turn stimulated NO release, resulting in an increase in gastric HCO3- secretion.
Bradykinin is also known to activate nociceptive-like afferent neurons through metabotropic G protein-coupled bradykinin B2 receptors [37, 38]. A previous study showed that binding to B2 receptors activated an intracellular signaling cascade, which led to the opening of TRPV1 channels . We found that bradykinin itself stimulated the secretion of HCO3- in the stomach in the present study. Furthermore, this response was attenuated not only by FR172357, the B2 antagonist, but also by indomethacin and L-NAME, which suggested the involvement of both PGs and NO in the response of HCO3- to bradykinin. The stimulatory effect of bradykinin was also significantly mitigated by the chemical ablation of capsaicin-sensitive afferent neurons, but was not affected by capsazepine, a TRPV1 antagonist. The stimulatory effect of bradykinin on HCO3- secretion is assumed to be partly mediated by sensory neurons via B2 receptors, but not through the interaction with TRPV1, in addition to endogenous PGs. Since bradykinin also potentiates the activation of TRPV1 by capsaicin through the hydrolysis of endogenous posphatidylinositol-4, 5-bisphosphate in a phospholipase C-dependent manner [39, 40], it is possible that capsaicin-induced gastric HCO3- secretion may be affected by the B2 receptor antagonist. However, the present study showed that the responses induced by capsaicin and acidification were not significantly affected by FR172357, which suggests that endogenous bradykinin has no role in these responses. The reason for these results has yet to be elucidated and is currently under investigation in our laboratory.
Capsaicin is assumed to stimulate the secretion of HCO3- in the stomach mediated by endogenous PGs and NO, as well as capsaicin-sensitive afferent neurons, but not bradykinin B2 receptors. Mucosal acidification also increased gastric HCO3- secretion through sensory neurons mediated by both PGs and NO, similar to capsaicin; however, their modes of action differed in terms of capsazepine-sensitivity and prostanoid receptor-dependency (Figure 9). Although luminal H+ played a modulator-type role in the physiological response mediated by capsaicin-sensitive afferent neurons in the stomach, it is likely that this action was not due to the interaction of H+ with the capsazepine-sensitive site of TRPV1, but resulted from the activation of ASIC3.
The authors are greatly indebted to Professor Shu Narumiya, Kyoto University Faculty of Medicine, for kindly supplying EP1, EP3, and IP receptor-knockout mice and Ono Pharmaceutical for supplying various EP agonists and antagonists. We also thank the undergraduate students at the Department of Pharmacology and Experimental Therapeutics, Kyoto Pharmaceutical University, Kyoto, Japan, for their technical collaboration.
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