Konturek S J, Tasler J, Cieszkowski M, Jaworek J, Coy D H, Schally A V
Gastroenterology. 1978 May;74(5 Pt 1):851-5.
The nature and extent of enkephalin- and morphine-induced inhibition of pancreatic bicarbonate and protein secretion were studied in dogs with chronic pancreatic fistulae after administering exogenous secretin or octapeptide of cholecystokinin and stimulants for the endogenous release of these hormones. Enkephalin and morphine competitively inhibited the pancreatic bicarbonate secretion induced either by exogenous secretin or duodenal acidification. This inhibition was partially reversed by naloxone, an opiate antagonist. Opiate substance also profoundly inhibited pancreatic protein response to octapeptide of cholecystokinin and to various stimulants of endogenous cholecystokinin release. We conclude that enkephalin and morphine strongly inhibit the pancreatic responses to exogenous and endogenous stimulants by a mechanism involving separate opiate receptors.
在给患有慢性胰瘘的犬类注射外源性促胰液素或胆囊收缩素八肽以及这些激素内源性释放的刺激剂后,研究了脑啡肽和吗啡对胰腺碳酸氢盐和蛋白质分泌的抑制性质及程度。脑啡肽和吗啡竞争性抑制外源性促胰液素或十二指肠酸化诱导的胰腺碳酸氢盐分泌。这种抑制作用被阿片拮抗剂纳洛酮部分逆转。阿片类物质也显著抑制胰腺对胆囊收缩素八肽以及内源性胆囊收缩素释放的各种刺激剂的蛋白质反应。我们得出结论,脑啡肽和吗啡通过涉及不同阿片受体的机制强烈抑制胰腺对外源性和内源性刺激剂的反应。