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艾塞那肽与摄食:可能的外周神经元途径。

Exenatide and feeding: possible peripheral neuronal pathways.

机构信息

Gastroenterology Laboratory, Department of Biomedical Sciences, College of Veterinary Medicine, Tuskegee University, Tuskegee, AL 36088, United States.

出版信息

Peptides. 2012 Feb;33(2):285-90. doi: 10.1016/j.peptides.2011.12.009. Epub 2011 Dec 24.

Abstract

Intraperitoneal (i.p.) administration of the synthetic agonist of the glucagon like peptide-1 (GLP-1) receptor exenatide reduces food intake. Here, we evaluated possible peripheral pathways for this reduction. Exenatide (0.5 μg/kg, i.p.) was given to three, overnight food-deprived, groups of rats: total subdiaphragmatic vagotomy (VGX, severs the vagus nerve), celiaco-mesenteric ganglionectomy (CMGX, severs the splanchnic nerve) and combined VGX/CMGX. Following the injection, meal sizes (MSs) and intermeal intervals (IMIs) were determined for a total of 120 min. We found that exenatide reduced the sizes of the first two meals but failed to prolong the IMI between them, that VGX attenuated the reduction of the first MS, and that VGX, CMGX and combined VGX/CMGX attenuated the reduction of the second MS by exenatide. Therefore, the vagus nerve appears necessary for the reduction of the first MS by exenatide, whereas both nerves appear necessary for the reduction of the second MS by this peptide.

摘要

腹腔内给予胰高血糖素样肽-1(GLP-1)受体激动剂艾塞那肽可减少食物摄入。在这里,我们评估了这种减少的可能的外周途径。给三组隔夜禁食的大鼠腹腔内给予艾塞那肽(0.5μg/kg):膈下迷走神经全切断术(VGX,切断迷走神经)、腹腔肠系膜神经节切除术(CMGX,切断内脏神经)和 VGX/CMGX 联合术。注射后,共测定 120 分钟的餐量(MS)和餐间间隔(IMI)。结果发现,艾塞那肽减少了前两餐的大小,但未能延长它们之间的 IMI,VGX 减弱了第一 MS 的减少,而 VGX、CMGX 和联合 VGX/CMGX 减弱了第二 MS 的减少。因此,迷走神经似乎是艾塞那肽减少第一 MS 的必需神经,而这两种神经对于这种肽减少第二 MS 都是必需的。

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