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下丘脑胃饥饿素信号传导介导奥氮平诱导的雌性大鼠食欲亢进和体重增加。

Hypothalamic ghrelin signalling mediates olanzapine-induced hyperphagia and weight gain in female rats.

作者信息

Zhang Qingsheng, He Meng, Deng Chao, Wang Hongqin, Lian Jiamei, Huang Xu-Feng

机构信息

Centre for Translational Neuroscience, School of Medicine, University of Wollongong, Wollongong, NSW, Australia.

出版信息

Int J Neuropsychopharmacol. 2014 May;17(5):807-18. doi: 10.1017/S1461145713001697. Epub 2014 Jan 27.

Abstract

Excessive weight gain is a major metabolic side effect of second-generation antipsychotics (SGAs) in the treatment of schizophrenia. Ghrelin is an orexigenic hormone secreted mainly from the stomach, which can induce weight gain and hyperphagia through regulating neuropeptides at the hypothalamus. Accumulating evidence implicates a relationship between ghrelin signalling and SGA-induced hyperphagia and weight gain. We report that olanzapine (a SGA with high weight gain liability) potently and time-dependently up-regulate ghrelin and ghrelin signalling, leading to hyperphagia and weight gain in female Sprague-Dawley rats, an action reversed by i.c.v. injection of a ghrelin receptor (GHS-R1a) antagonist. These findings indicate a crucial role of ghrelin signalling in hyperphagia induced by olanzapine, supporting the notion that GHS-R1a antagonist may be useful for pharmacological treatment of SGA-induced weight gain resulted from hyperphagia.

摘要

体重过度增加是第二代抗精神病药物(SGA)治疗精神分裂症时的主要代谢副作用。胃饥饿素是一种主要由胃分泌的促食欲激素,它可通过调节下丘脑的神经肽来诱导体重增加和食欲亢进。越来越多的证据表明胃饥饿素信号与SGA诱导的食欲亢进和体重增加之间存在关联。我们报告称,奥氮平(一种具有高体重增加倾向的SGA)能有效且呈时间依赖性地上调胃饥饿素及胃饥饿素信号,导致雌性Sprague-Dawley大鼠出现食欲亢进和体重增加,而脑室内注射胃饥饿素受体(GHS-R1a)拮抗剂可逆转这一作用。这些发现表明胃饥饿素信号在奥氮平诱导的食欲亢进中起关键作用,支持了GHS-R1a拮抗剂可能有助于药物治疗因食欲亢进导致的SGA诱导体重增加这一观点。

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