Improta G, Broccardo M
Institute of Pharmacology III, University La Sapienza, Rome, Italy.
Peptides. 1988 Jul-Aug;9(4):843-6. doi: 10.1016/0196-9781(88)90131-3.
Intracerebroventricular (ICV) and subcutaneous (SC) injections of sauvagine powerfully inhibited gastric acid secretion stimulated by gastric distension and by 2-deoxy-D-glucose, but not by histamine in pylorus-ligated rats. Naloxone failed to antagonize the antisecretory effects of SC and ICV sauvagine. Intravenous infusion of sauvagine completely suppressed bethanechol-stimulated gastric secretion, significantly decreased pentagastrin-stimulated gastric secretion and did not modify histamine-stimulated gastric secretion in gastric-perfused rats. The inhibitory effect of sauvagine on gastric secretory response is not mediated through opioid or histamine receptors. It appears to be dependent on a vagal mechanism as well as other mechanisms that await further elucidation.
在幽门结扎的大鼠中,脑室内(ICV)和皮下(SC)注射蛙皮素可强烈抑制胃扩张和2-脱氧-D-葡萄糖刺激的胃酸分泌,但对组胺刺激的胃酸分泌无抑制作用。纳洛酮未能拮抗皮下和脑室内注射蛙皮素的抗分泌作用。在胃灌注的大鼠中,静脉输注蛙皮素可完全抑制氨甲酰甲胆碱刺激的胃液分泌,显著降低五肽胃泌素刺激的胃液分泌,而对组胺刺激的胃液分泌无影响。蛙皮素对胃分泌反应的抑制作用不是通过阿片类或组胺受体介导的。它似乎依赖于迷走神经机制以及其他有待进一步阐明的机制。