McTigue D M, Rogers R C
Department of Physiology, College of Medicine, Ohio State University, Columbus 43210, USA.
Neurosci Lett. 1995 Mar 24;188(2):93-6. doi: 10.1016/0304-3940(95)11404-k.
The present study examined the influence of peripherally administered pancreatic polypeptide (PP) on vagal control of gastric motility. The jugular vein was cannulated in urethane-anesthetized rats and a strain gauge was sewn onto the antrum to monitor motility. Intravenous infusion of rat PP (2-200 pmol over 45 min) resulted in a dose-dependent increase in antral contraction amplitude. The motility response to i.v. PP was eliminated by pretreatment with atropine or bilateral vagotomy. In contrast to i.v. infusion, close intra-arterial infusion of PP into the gastric circulation had no effect on motility suggesting that PP does not act upon peripheral afferent terminals or directly within the stomach. These results support the hypothesis that circulating PP indirectly enhances gastric motility through a vagal cholinergic mechanism.
本研究检测了外周给予胰多肽(PP)对胃动力迷走神经控制的影响。在氨基甲酸乙酯麻醉的大鼠中插入颈静脉导管,并将应变片缝在胃窦上以监测动力。静脉输注大鼠PP(45分钟内2 - 200皮摩尔)导致胃窦收缩幅度呈剂量依赖性增加。静脉注射PP的动力反应可通过阿托品预处理或双侧迷走神经切断术消除。与静脉输注相反,将PP经动脉近距离注入胃循环对动力没有影响,这表明PP不作用于外周传入神经末梢或不在胃内直接起作用。这些结果支持以下假说:循环中的PP通过迷走胆碱能机制间接增强胃动力。