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外源性瘦素通过十二指肠CCK1-迷走神经依赖机制抑制麻醉大鼠胰液的分泌。

Exogenous leptin inhibits the secretion of pancreatic juice via a duodenal CCK1-vagal-dependent mechanism in anaesthetized rats.

作者信息

Matyjek R, Herzig K-H, Kato S, Zabielski R

机构信息

The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, 05-110 Jablonna, Poland.

出版信息

Regul Pept. 2003 Jun 15;114(1):15-20. doi: 10.1016/s0167-0115(03)00064-8.

Abstract

Leptin originally described as product of the ob gene has been shown to be expressed in various tissues including the gastrointestinal tract. In this study, we investigated the influence of leptin on the secretion of pancreatic juice in biliary-pancreatic duct cannulated anaesthetised rats and in dispersed rat pancreatic acini in vitro. Exogenous leptin was given in boluses intravenously with or without CCK-8 (12 pmol kg(-1) body weight) in the presence or absence pharmacological CCK(1) receptor blockade, cervical vagotomy, and capsaicin pre-treatment. Administration of leptin (0.1, 1 and 10 microg kg(-1) body weight) did not affect the volume of bile and pancreatic juice while the protein and trypsin outputs were reduced in a dose-dependent manner. In the rats, leptin inhibited CCK-8 stimulated protein and trypsin outputs stronger than the basal pancreatic secretion. The inhibition by leptin was abolished by the pharmacological CCK(1) receptor blockade, cervical vagotomy, and capsaicin pre-treatment. In contrast, leptin did not affect basal and CCK-8-stimulated amylase release from the dispersed rat pancreatic acini in vitro. In conclusion, the results of the present study suggest that leptin does not act directly on the rat pancreatic acinar cells but inhibits the secretion of pancreatic enzymes acting indirectly via a neurohormonal CCK-vagal-dependent mechanism.

摘要

瘦素最初被描述为肥胖基因的产物,已被证明在包括胃肠道在内的各种组织中表达。在本研究中,我们研究了瘦素对胆管-胰管插管麻醉大鼠和体外分散的大鼠胰腺腺泡胰液分泌的影响。在存在或不存在药理学CCK(1)受体阻断、颈迷走神经切断术和辣椒素预处理的情况下,静脉推注外源性瘦素,同时给予或不给予CCK-8(12 pmol kg(-1)体重)。给予瘦素(0.1、1和10 μg kg(-1)体重)不影响胆汁和胰液的体积,而蛋白质和胰蛋白酶的分泌量呈剂量依赖性降低。在大鼠中,瘦素抑制CCK-8刺激的蛋白质和胰蛋白酶分泌,其作用强于基础胰腺分泌。瘦素的抑制作用可通过药理学CCK(1)受体阻断、颈迷走神经切断术和辣椒素预处理消除。相反,瘦素在体外不影响分散的大鼠胰腺腺泡基础和CCK-8刺激的淀粉酶释放。总之,本研究结果表明,瘦素不直接作用于大鼠胰腺腺泡细胞,而是通过神经激素CCK-迷走神经依赖性机制间接抑制胰腺酶的分泌。

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