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通过雄性大鼠迷走神经背核中 mTOR 信号对食物摄入的调节:关注 ghrelin 和 nesfatin-1。

Modulation of food intake by mTOR signalling in the dorsal motor nucleus of the vagus in male rats: focus on ghrelin and nesfatin-1.

机构信息

W. Zhang: University of Michigan, Department of Surgery, 1150 West Medical Center Drive, 1520B MSRB I, Ann Arbor, MI 48109, USA.

出版信息

Exp Physiol. 2013 Dec;98(12):1696-704. doi: 10.1113/expphysiol.2013.074930. Epub 2013 Aug 16.

Abstract

Previous studies have demonstrated that mammalian target of rapamycin (mTOR) signalling in the hypothalamus is involved in the control of energy homeostasis. The aim of this study was to characterize the effect of mTOR signalling in the dorsal motor nucleus of the vagus (DMNV) on energy intake. Phospho-mTOR was detected in the DMNV neurons, and its levels were increased by energy deprivation. Rapamycin significantly inhibited mTOR activity and reduced food intake when administrated into the fourth ventricle. Exposure of DMNV neurons to ghrelin increased the phosphorylation of mTOR. Injection of ghrelin into the fourth ventricle significantly increased food intake relative to the control vehicle. Pretreatment with rapamycin for 15 min attenuated the orexigenic effect of ghrelin. A reduction in the phosphorylation of mTOR was observed following injection of nesfatin-1 into the fourth ventricle. When administrated by injection into the fourth ventricle, nesfatin-1 suppressed food intake in comparison with the control vehicle. The anorexigenic effect of nesfatin-1 was significantly attenuated by pretreatment with leucine for 15 min. All these findings suggest that mTOR signalling in the DMNV neurons regulates both the nutrient and the hormonal signals for the modulation of food intake.

摘要

先前的研究表明,哺乳动物雷帕霉素靶蛋白(mTOR)信号在下丘脑参与能量平衡的控制。本研究的目的是描述迷走神经背核(DMNV)中 mTOR 信号对能量摄入的影响。在 DMNV 神经元中检测到磷酸化 mTOR,并且其水平在能量剥夺时增加。雷帕霉素在第四脑室给药时可显著抑制 mTOR 活性并减少食物摄入。给予 DMNV 神经元 ghrelin 可增加 mTOR 的磷酸化。与对照载体相比,ghrelin 注入第四脑室可显著增加食物摄入。雷帕霉素预处理 15 分钟可减弱 ghrelin 的食欲增强作用。nesfatin-1 注入第四脑室后,mTOR 的磷酸化减少。与对照载体相比,nesfatin-1 经第四脑室给药可抑制食物摄入。亮氨酸预处理 15 分钟可显著减弱 nesfatin-1 的厌食作用。所有这些发现表明,DMNV 神经元中的 mTOR 信号调节了营养素和激素信号,以调节食物摄入。

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