Manso M A, Rodriguez A I, Garcia-Montero A C, De Dios I
Departamento de Fisiología y Farmacología, Facultad de Biología, Universidad de Salamanca, Spain.
Arch Physiol Biochem. 1995 Aug;103(4):410-5. doi: 10.3109/13813459509047130.
The role of cholecystokinin (CCK) in the development of a necrotizing acute pancreatitis induced by a diet deficient in choline and supplemented with ethionine (CDE) has been evaluated in the rat by using a potent CCK receptor antagonist L-364,718. Acute pancreatitis was induced by administration of CDE diet for 14 days. L-364,718 administration was carried out by subcutaneous injections at dose of 0.1 mg/kg/day. Pancreatic exocrine secretion (flow, protein, amylase and trypsin outputs) in resting and under infusion of 1.25 microgram/kg/h of CCK-8 were used to evaluate the pancreatic functionality. Others parameters (serum amylase, percentage fluid in pancreas, haematocrit and mortality) evaluated the severity of pancreatitis. L-364,718 slightly reduced the mortality and the increases of percentage of fluid accumulated in pancreas in CDE diet acute pancreatitis. Basal and CCK stimulated pancreatic secretion was significantly depressed 36 hours after L-364,718 treatment. A slight response to CCK was observed. Nevertheless it was lower than usually observed in control rats. Our results demonstrate that in the rat, chronic L-364,718 treatment did not completely restore pancreatic activity in acute pancreatitis induced by CDE diet. Hence CCK cannot be considered as the main factor involved in the development of this pancreatitis model.
通过使用一种强效的胆囊收缩素(CCK)受体拮抗剂L-364,718,在大鼠中评估了CCK在由胆碱缺乏并补充乙硫氨酸(CDE)的饮食诱导的坏死性急性胰腺炎发展过程中的作用。通过给予CDE饮食14天来诱导急性胰腺炎。以0.1毫克/千克/天的剂量通过皮下注射给予L-364,718。在静息状态下以及在以1.25微克/千克/小时的速度输注CCK-8时的胰腺外分泌(流量、蛋白质、淀粉酶和胰蛋白酶输出量)被用于评估胰腺功能。其他参数(血清淀粉酶、胰腺中的液体百分比、血细胞比容和死亡率)用于评估胰腺炎的严重程度。L-364,718略微降低了CDE饮食急性胰腺炎中的死亡率以及胰腺中积聚的液体百分比的增加。在L-364,718治疗36小时后,基础状态下以及CCK刺激的胰腺分泌显著降低。观察到对CCK有轻微反应。然而,该反应低于在对照大鼠中通常观察到的反应。我们的结果表明,在大鼠中,慢性L-364,718治疗并未完全恢复由CDE饮食诱导的急性胰腺炎中的胰腺活性。因此,CCK不能被视为参与该胰腺炎模型发展的主要因素。