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腹内侧下丘脑的α/β水解酶结构域6控制能量代谢灵活性。

α/β-Hydrolase Domain 6 in the Ventromedial Hypothalamus Controls Energy Metabolism Flexibility.

作者信息

Fisette Alexandre, Tobin Stephanie, Décarie-Spain Léa, Bouyakdan Khalil, Peyot Marie-Line, Madiraju S R Murthy, Prentki Marc, Fulton Stephanie, Alquier Thierry

机构信息

CRCHUM and Montreal Diabetes Research Center, Université de Montréal, Montreal, QC H3T1J4, Canada; Department of Nutrition, Université de Montréal, Montreal, QC H3T1J4, Canada.

CRCHUM and Montreal Diabetes Research Center, Université de Montréal, Montreal, QC H3T1J4, Canada; Department of Neuroscience, Université de Montréal, Montreal, QC H3T1J4, Canada.

出版信息

Cell Rep. 2016 Oct 25;17(5):1217-1226. doi: 10.1016/j.celrep.2016.10.004.

Abstract

α/β-Hydrolase domain 6 (ABHD6) is a monoacylglycerol hydrolase that degrades the endocannabinoid 2-arachidonoylglycerol (2-AG). Although complete or peripheral ABHD6 loss of function is protective against diet-induced obesity and insulin resistance, the role of ABHD6 in the central control of energy balance is unknown. Using a viral-mediated knockout approach, targeted endocannabinoid measures, and pharmacology, we discovered that mice lacking ABHD6 from neurons of the ventromedial hypothalamus (VMH) have higher VMH 2-AG levels in conditions of endocannabinoid recruitment and fail to physiologically adapt to key metabolic challenges. VMH mice exhibited blunted fasting-induced feeding and reduced food intake, energy expenditure, and adaptive thermogenesis in response to cold exposure, high-fat feeding, and dieting (transition to a low-fat diet). Our findings identify ABHD6 as a regulator of the counter-regulatory responses to major metabolic shifts, including fasting, nutrient excess, cold, and dieting, thereby highlighting the importance of ABHD6 in the VMH in mediating energy metabolism flexibility.

摘要

α/β水解酶结构域6(ABHD6)是一种单酰基甘油水解酶,可降解内源性大麻素2-花生四烯酸甘油酯(2-AG)。尽管ABHD6功能的完全丧失或外周丧失对饮食诱导的肥胖和胰岛素抵抗具有保护作用,但ABHD6在能量平衡中枢控制中的作用尚不清楚。通过病毒介导的基因敲除方法、靶向内源性大麻素检测和药理学研究,我们发现,在下丘脑腹内侧核(VMH)神经元中缺乏ABHD6的小鼠,在内源性大麻素募集的情况下,VMH中的2-AG水平较高,并且无法在生理上适应关键的代谢挑战。VMH基因敲除小鼠表现出空腹诱导的进食反应迟钝,在冷暴露、高脂喂养和节食(过渡到低脂饮食)时食物摄入量、能量消耗和适应性产热减少。我们的研究结果表明,ABHD6是对主要代谢变化(包括禁食、营养过剩、寒冷和节食)的反调节反应的调节因子,从而突出了ABHD6在VMH中介导能量代谢灵活性的重要性。

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