Takács T, Pap A
First Department of Medicine, Albert Szent-Györgyi Medical University, Szeged, Hungary.
Int J Pancreatol. 1991 Sep;10(1):1-8. doi: 10.1007/BF02924248.
In this article, the effects of different classes of cholecystokinin (CCK) receptor antagonists in CCK-related physiological processes of the pancreas have been discussed. Both glutaramic acid derivatives and natural (benzodiazepine) analogs are potent, competitive antagonists of peripheral CCK receptors. These compounds thus provide a powerful tool for investigating the physiological and pharmacological actions of CCK in the gastrointestinal system, and have already clarified the role of CCK in pancreatic secretion and trophism or growth.
在本文中,已讨论了不同类别的胆囊收缩素(CCK)受体拮抗剂在胰腺CCK相关生理过程中的作用。谷氨酸衍生物和天然(苯二氮卓)类似物都是外周CCK受体的强效竞争性拮抗剂。因此,这些化合物为研究CCK在胃肠系统中的生理和药理作用提供了有力工具,并且已经阐明了CCK在胰腺分泌、营养作用或生长中的作用。