Role of cholecystokinin in the development and progression of acute pancreatitis and the potential of therapeutic application of cholecystokinin receptor antagonists

被引:13
作者
Niederau, C
Grendell, JH
机构
[1] St Josef Hosp, Acad Teaching Hosp, Dept Internal Med, D-46045 Oberhausen, Germany
[2] Cornell Univ, Coll Med, New York, NY USA
[3] New York Hosp, Dept Med, Div Gastroenterol, New York, NY 10021 USA
关键词
pancreatitis; cholecystokinin; cholecystokinin receptor; caerulein; pancreatic secretion;
D O I
10.1159/000051458
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
There is also evidence that CCK antagonists have a potential therapeutic benefit. Clinical studies will evaluate their therapeutic potential for patients with AP. This presentation reviews the role of cholecystokinin (CCK) as a contributory factor for the development and progression of acute pancreatitis (AP) and the perspective of CCK receptor antagonists for treatment of AP. High, supraphysiological concentrations of CCK induce AP in various species including man. There is also evidence that physiological increases in plasma CCK deteriorates AP in several animal models. The latter findings support the hypothesis that CCK plays a contributory or permissive role for the development of AP. The majorities of experimental studies show that the prophylactic and therapeutic use of CCK antagonists ameliorates AP. The latter effects were clearly shown for models of biliary AP in which plasma CCK is increased due to a feedback mechanism. However, CCK antagonists also had beneficial effects in models in which plasma CCK is; not increased. In animal strains which do not have a CCK-A-receptor due to a genetic abnormality AP induced by a certain noxious factor does not develop to the same severity when compared to animals with a normal CCKA-receptor. Thus, CCK acts as a permissive or contributory factor for the development and progression of AP. There is also evidence that CCK antagonists have a potential therapeutic benefit. Clinical studies will evaluate their therapeutic potential for patients with AP.
引用
收藏
页码:69 / 74
页数:6
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