Champion M C, Sullivan S N, Bloom S R, Adrian T E, Christofides N D
Am J Gastroenterol. 1982 Sep;77(9):617-20.
Postprandial gastrointestinal hormone secretion was not affected by the intravenous administration of naloxone. However, after the administration of morphine, multiple effects were observed. Postprandial pancreatic polypeptide, motilin, and enteroglucagon secretion were abolished and there was a reduction in the secretion of insulin, gastric inhibitory polypeptide, and neurotensin. There was prolonged secretion of gastrin. Levels of vasoactive intestinal polypeptide, somatostatin, and pancreatic glucagon were not affected. Many of these changes can be accounted for by the ability of morphine to delay gastric emptying. The prolonged secretion of gastrin could result from a combination of impaired gastric emptying and reduced postprandial gastric acid secretion. Inhibition of vagal acetylcholine release is the most likely explanation for the abolition of pancreatic polypeptide secretion. With the exception of the effects on motilin, pancreatic polypeptide, and enteroglucagon secretion this study provides no evidence that opiate substances directly affect the secretion of gastrointestinal hormones.
静脉注射纳洛酮对餐后胃肠激素分泌没有影响。然而,注射吗啡后,观察到多种效应。餐后胰多肽、胃动素和肠高血糖素分泌被抑制,胰岛素、胃抑肽和神经降压素分泌减少。胃泌素分泌延长。血管活性肠肽、生长抑素和胰高血糖素水平未受影响。这些变化中的许多可以用吗啡延迟胃排空的能力来解释。胃泌素分泌延长可能是胃排空受损和餐后胃酸分泌减少共同作用的结果。迷走神经乙酰胆碱释放受抑制最有可能是胰多肽分泌受抑制的原因。除了对胃动素、胰多肽和肠高血糖素分泌的影响外,本研究没有证据表明阿片类物质直接影响胃肠激素的分泌。