Adler G, Beglinger C, Braun U, Reinshagen M, Koop I, Schafmayer A
Department of Internal Medicine, Phillips University, Marburg, F.R.G.
Regul Pept. 1990 Sep 10;30(2):105-11. doi: 10.1016/0167-0115(90)90051-w.
The purpose of this study was to determine the role of CCK during the intestinal phase of pancreatic polypeptide (PP) release in man. We first compared the PP response to exogenous caerulein infusion in the presence or absence of either loxiglumide (a specific CCK antagonist) or atropine in six healthy subjects. In the second part of the study, a meal was perfused to the duodenum with and without either loxiglumide or atropine. Both loxiglumide and atropine completely abolished the PP response to exogenous or endogenous stimulation (P less than 0.05). We conclude that CCK participates in the intestinal phase of PP secretion.
本研究的目的是确定胆囊收缩素(CCK)在人类胰腺多肽(PP)释放的肠期所起的作用。我们首先在6名健康受试者中比较了在有或没有洛西格列胺(一种特异性CCK拮抗剂)或阿托品的情况下,外源性蛙皮素输注后PP的反应。在研究的第二部分,在有或没有洛西格列胺或阿托品的情况下,将一顿饭灌注到十二指肠。洛西格列胺和阿托品均完全消除了PP对外源性或内源性刺激的反应(P<0.05)。我们得出结论,CCK参与了PP分泌的肠期。