Muto N, Eguchi R, Akagi Y, Itoh N, Tanaka K
Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Japan.
Res Commun Mol Pathol Pharmacol. 1998 Aug;101(2):127-36.
We have previously demonstrated that endogenous ascorbic acid is secreted into the gastric lumen by cholinergic stimulation in both conscious pylorus-ligated rats and the perfused stomach of unconscious rats, and that gastrin, a potent gastric stimulatory peptide hormone, has no effect. In the present study, the effects of some gastrointestinal peptide hormones on gastric ascorbic acid secretion were further examined in the perfused stomach of rats. An intravenous administration of cholecystokinin octapeptide (CCK-8) significantly increased gastric ascorbic acid secretion at a dose of 1.0 and 4.0 micrograms/kg, whereas the other three peptides examined, bombesin, neurotensin and substance P, showed no or little effect at the doses which were quite commonly employed for evaluation of various gastric functions. CCK-8-induced ascorbic acid secretion was reduced by pretreatment with proglumide, which is a CCK receptor antagonist, but not by pretreatment with atropine. These results indicate that gastric ascorbic acid secretion is physiologically regulated not only by muscarinic receptor-associated cholinergic stimulation but also by CCK receptor-associated humoral stimulation.
我们之前已经证明,在清醒的幽门结扎大鼠和麻醉大鼠的灌流胃中,内源性抗坏血酸可通过胆碱能刺激分泌到胃腔中,而胃泌素(一种强效的胃刺激肽激素)则无此作用。在本研究中,我们在大鼠的灌流胃中进一步研究了一些胃肠肽激素对胃抗坏血酸分泌的影响。静脉注射八肽胆囊收缩素(CCK-8),剂量为1.0和4.0微克/千克时,可显著增加胃抗坏血酸的分泌,而所检测的其他三种肽,即蛙皮素、神经降压素和P物质,在用于评估各种胃功能的常用剂量下均无作用或作用很小。CCK-8诱导的抗坏血酸分泌可被CCK受体拮抗剂丙谷胺预处理所抑制,但不受阿托品预处理的影响。这些结果表明,胃抗坏血酸的分泌不仅受到与毒蕈碱受体相关的胆碱能刺激的生理调节,还受到与CCK受体相关的体液刺激的调节。