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外周给予的胆囊收缩素八肽对大鼠脑干神经元的作用机制

Mechanisms of action of peripherally administered cholecystokinin octapeptide on brain stem neurons in the rat.

作者信息

Raybould H E, Gayton R J, Dockray G J

机构信息

MRC Secretory Control Group, Physiological Laboratory, University of Liverpool, UK.

出版信息

J Neurosci. 1988 Aug;8(8):3018-24. doi: 10.1523/JNEUROSCI.08-08-03018.1988.

DOI:10.1523/JNEUROSCI.08-08-03018.1988
PMID:3411366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6569407/
Abstract

We have investigated the pathway and the mechanism by which cholecystokinin octapeptide (CCK-8), given systemically, may influence the discharge of brain stem neurons that have an input from the stomach. Extracellular recordings were made from neurons in the nucleus of the solitary tract (NTS), where vagal afferents terminate, and from neighboring regions of the dorsal medial medulla. Gastric distension and CCK-8 injected intra-aortically close to the stomach evoked either excitatory or inhibitory responses that were abolished by cervical vagal section. In animals from which the celiac/superior mesenteric ganglia were removed, or the gastric antrum resected 2 weeks earlier, responses to gastric distension and CCK-8 were maintained. The effects of CCK-8 are unlikely to be secondary to changes in smooth muscle tone because CCK-8 decreased pressure in the body of the stomach, while distension increased it. Moreover, intravenous noradrenaline and vasoactive intestinal peptide had effects similar to CCK-8 on intragastric pressure, but evoked different patterns of responses from brain stem neurons. The results are consistent with the idea that CCK-8 acts directly on vagal mechanoreceptive endings in the gastric corpus wall. It is well known that peripheral administration of CCK-8 influences short-term regulation of food intake. The effects described here may reflect the pathway by which peripheral CCK influences CNS function.

摘要

我们研究了全身给予八肽胆囊收缩素(CCK - 8)可能影响来自胃的脑干神经元放电的途径和机制。在迷走神经传入纤维终止的孤束核(NTS)神经元以及延髓背内侧的相邻区域进行了细胞外记录。胃扩张和在靠近胃的主动脉内注射CCK - 8可诱发兴奋性或抑制性反应,这些反应在颈迷走神经切断后消失。在切除腹腔/肠系膜上神经节的动物或两周前切除胃窦的动物中,对胃扩张和CCK - 8的反应得以维持。CCK - 8的作用不太可能继发于平滑肌张力的变化,因为CCK - 8可降低胃体压力,而扩张则使其升高。此外,静脉注射去甲肾上腺素和血管活性肠肽对胃内压的作用与CCK - 8相似,但诱发的脑干神经元反应模式不同。结果与CCK - 8直接作用于胃体壁迷走机械感受末梢的观点一致。众所周知,外周给予CCK - 8会影响食物摄入的短期调节。这里描述的作用可能反映了外周CCK影响中枢神经系统功能的途径。