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γ-氨基丁酸与进食:通过中枢γ-氨基丁酸转氨酶抑制作用逆转暴饮暴食

GABA and feeding: reversal of overeating by central GABA-transaminase inhibition.

作者信息

Coscina D V

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1983;7(4-6):463-7. doi: 10.1016/0278-5846(83)90012-x.

Abstract

Past literature is reviewed briefly which suggests that variations in brain GABA metabolism may be involved in the control of food intake in rats. Recent experiments from the author's laboratory are summarized in which brain GABA has been elevated in adult female rats by intracisternal injection of the GABA-transaminase inhibitor, ethanolamine-O-sulfate (EOS). Central EOS pretreatment produced dose-dependent anorexia in normal subjects and prevented acute overeating in response to systemic insulin (12 U/kg) or 2-deoxyglucose (750 mg/kg). Similar EOS pretreatment essentially reversed the chronic overeating induced by diet palatability, bilateral medial hypothalamic lesions or genetic predisposition (in Zucker fatty rats). The ubiquity of these anorexic effects in the absence of clear motor debilitation suggests that drugs which elevate brain GABA deserve further investigation for their potential utility in the clinical treatment of overeating.

摘要

本文简要回顾了以往的文献,这些文献表明大脑γ-氨基丁酸(GABA)代谢的变化可能参与大鼠食物摄入的控制。作者实验室最近的实验总结如下:通过脑池内注射GABA转氨酶抑制剂乙醇胺-O-硫酸盐(EOS),成年雌性大鼠大脑中的GABA水平升高。中枢EOS预处理在正常受试者中产生剂量依赖性厌食,并防止对全身胰岛素(12 U/kg)或2-脱氧葡萄糖(750 mg/kg)的急性暴饮暴食。类似的EOS预处理基本上逆转了由饮食适口性、双侧下丘脑内侧损伤或遗传易感性(在 Zucker 肥胖大鼠中)引起的慢性暴饮暴食。在没有明显运动功能障碍的情况下,这些厌食作用的普遍性表明,提高大脑GABA水平的药物因其在临床治疗暴饮暴食方面的潜在效用值得进一步研究。

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