Schafmayer A, Nustede R, Köhler H
Department of Surgery, Hospital Luneberg, Georg-August University, Göttingen, Germany.
Pancreas. 1993 Sep;8(5):627-31. doi: 10.1097/00006676-199309000-00016.
Important basic physiological mechanisms of exocrine pancreas secretion were delineated in a canine model. However, dogs have been considered unsuitable for the study of the controversial feedback regulation of exocrine pancreas secretion. The present study reveals a marked modification of pancreas secretion following the intraduodenal instillation of lipase: The postprandial lipase secretion decreases from 2,421 U x 180 min-1 to 1,490 U x 180 min-1, but simultaneously determined cholecystokinin (CCK) concentrations in plasma do not increase under these circumstances. The intraduodenal application of a protease inhibitor (800 mg camostate) significantly stimulates the secretion of the exocrine pancreas in the fasting dog: After 15 min the protein release increased to 133 +/- 30 mg. Intravenous atropine blocks this increase. The plasma concentrations of CCK are not significantly influenced. These results in our canine model show that the secretory activity of the exocrine pancreas depends on the intraduodenal enzyme content. CCK is irrelevant in this context.
外分泌胰腺分泌的重要基本生理机制在犬类模型中得到了阐明。然而,犬类一直被认为不适用于研究外分泌胰腺分泌存在争议的反馈调节。本研究揭示了十二指肠内注入脂肪酶后胰腺分泌的显著变化:餐后脂肪酶分泌从2421 U×180分钟-1降至1490 U×180分钟-1,但在这些情况下同时测定的血浆中胆囊收缩素(CCK)浓度并未增加。十二指肠内应用蛋白酶抑制剂(800 mg卡莫司他)可显著刺激禁食犬的外分泌胰腺分泌:15分钟后蛋白质释放增加至133±30 mg。静脉注射阿托品可阻断这种增加。CCK的血浆浓度未受到显著影响。我们犬类模型中的这些结果表明,外分泌胰腺的分泌活性取决于十二指肠内的酶含量。在这种情况下,CCK无关紧要。