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S6K1 在中枢神经系统中通过 MC4R/CRH 通路调节能量消耗,以响应必需氨基酸的剥夺。

S6K1 in the central nervous system regulates energy expenditure via MC4R/CRH pathways in response to deprivation of an essential amino acid.

机构信息

Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Graduate School of the Chinese Academy of Sciences, Shanghai, China.

出版信息

Diabetes. 2012 Oct;61(10):2461-71. doi: 10.2337/db11-1278. Epub 2012 Jul 10.

Abstract

It is well established that the central nervous system (CNS), especially the hypothalamus, plays an important role in regulating energy homeostasis and lipid metabolism. We have previously shown that hypothalamic corticotropin-releasing hormone (CRH) is critical for stimulating fat loss in response to dietary leucine deprivation. The molecular mechanisms underlying the CNS regulation of leucine deprivation-stimulated fat loss are, however, still largely unknown. Here, we used intracerebroventricular injection of adenoviral vectors to identify a novel role for hypothalamic p70 S6 kinase 1 (S6K1), a major downstream effector of the kinase mammalian target of rapamycin, in leucine deprivation stimulation of energy expenditure. Furthermore, we show that the effect of hypothalamic S6K1 is mediated by modulation of Crh expression in a melanocortin-4 receptor-dependent manner. Taken together, our studies provide a new perspective for understanding the regulation of energy expenditure by the CNS and the importance of cross-talk between nutritional control and regulation of endocrine signals.

摘要

众所周知,中枢神经系统(CNS),特别是下丘脑,在调节能量平衡和脂质代谢方面发挥着重要作用。我们之前已经表明,下丘脑促肾上腺皮质激素释放激素(CRH)对于刺激脂肪损失以响应膳食亮氨酸缺乏至关重要。然而,中枢神经系统调节亮氨酸缺乏刺激的脂肪损失的分子机制在很大程度上仍然未知。在这里,我们使用脑室内注射腺病毒载体来鉴定下丘脑 p70 S6 激酶 1(S6K1)的新作用,S6K1 是哺乳动物雷帕霉素靶蛋白激酶的主要下游效应物,在亮氨酸缺乏刺激能量消耗中发挥作用。此外,我们表明,下丘脑 S6K1 的作用是通过以黑素皮质素 4 受体依赖性方式调节 Crh 表达来介导的。总之,我们的研究为理解中枢神经系统对能量消耗的调节以及营养控制和内分泌信号调节之间的相互作用提供了新的视角。

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