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Obesity-driven synaptic remodeling affects endocannabinoid control of orexinergic neurons.肥胖驱动的突触重构影响内源性大麻素对食欲素神经元的控制。
Proc Natl Acad Sci U S A. 2013 Jun 11;110(24):E2229-38. doi: 10.1073/pnas.1219485110. Epub 2013 Apr 29.
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The endocannabinoid system in energy homeostasis and the etiopathology of metabolic disorders.内源性大麻素系统在能量平衡和代谢紊乱的发病机制中的作用。
Cell Metab. 2013 Apr 2;17(4):475-90. doi: 10.1016/j.cmet.2013.03.001.
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Autocrine endocannabinoid signaling through CB1 receptors potentiates OX1 orexin receptor signaling.自分泌内源性大麻素信号通过 CB1 受体增强 OX1 食欲素受体信号。
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A novel fluorophosphonate inhibitor of the biosynthesis of the endocannabinoid 2-arachidonoylglycerol with potential anti-obesity effects.一种新型氟膦酸酯类内源性大麻素 2-花生四烯酸甘油的生物合成抑制剂,具有潜在的抗肥胖作用。
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Synaptic plasticity in neuronal circuits regulating energy balance.神经元回路中调节能量平衡的突触可塑性。
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Peripheral cannabinoid-1 receptor inverse agonism reduces obesity by reversing leptin resistance.外周型大麻素 1 型受体反向激动剂通过逆转瘦素抵抗减轻肥胖。
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Short term voluntary overfeeding disrupts brain insulin control of adipose tissue lipolysis.短期自愿过度进食会破坏大脑胰岛素对脂肪组织脂解的控制。
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Hypothalamic CB1 cannabinoid receptors regulate energy balance in mice.下丘脑 CB1 cannabinoid 受体调节小鼠的能量平衡。
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Hypothalamic 2-arachidonoylglycerol regulates multistage process of high-fat diet preferences.下丘脑 2-花生四烯酸甘油调节高脂肪饮食偏好的多阶段过程。
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10
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大麻素CB1受体在美味食物摄入、肥胖及相关代谢紊乱中作用的新视野。

New horizons on the role of cannabinoid CB1 receptors in palatable food intake, obesity and related dysmetabolism.

作者信息

Cristino L, Palomba L, Di Marzo V

机构信息

Endocannabinoid Research Group, Institute of Biomolecular Chemistry, Consiglio Nazionale delle Ricerche , Pozzuoli, Italy.

Department of Biomolecular Sciences, University 'Carlo Bo' , Urbino, Italy.

出版信息

Int J Obes Suppl. 2014 Jul;4(Suppl 1):S26-30. doi: 10.1038/ijosup.2014.8. Epub 2014 Jul 8.

DOI:10.1038/ijosup.2014.8
PMID:27152162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4850587/
Abstract

Excessive consumption of high-energy, palatable food contributes to obesity, which results in the metabolic syndrome, heart disease, type-2 diabetes and death. Current knowledge on the function of the hypothalamus as the brain 'feeding centre' recognizes this region as the main regulator of body weight in the central nervous system. Because of their intrinsically fast and adaptive activities, feeding-controlling neural circuitries are endowed with synaptic plasticity modulated by neurotransmitters and hormones that act at different hierarchical levels of integration. In the hypothalamus, among the chemical mediators involved in this integration, endocannabinoids (eCBs) are ideal candidates for the fast (that is, non-genomic), stress-related fine-tuning of neuronal functions. In this article, we overview the role of the eCB system (ECS) in the control of energy intake, and particularly in the consumption of high-energy, palatable food, and discuss how such a role is affected in the brain by changes in the levels of feeding-regulated hormones, such as the adipose tissue-derived anorexigenic mediator leptin, as well as by high-fat diets. The understanding of the molecular mechanisms underlying the neuronal control of feeding behaviours by eCBs offers many potential opportunities for novel therapeutic approaches against obesity. Highlights of the latest advances in the development of strategies that minimize central ECS overactivity in 'western diet'-driven obesity are discussed.

摘要

过量食用高能量、美味的食物会导致肥胖,进而引发代谢综合征、心脏病、2型糖尿病甚至死亡。目前关于下丘脑作为大脑“进食中枢”功能的认识,将该区域视为中枢神经系统中体重的主要调节者。由于其内在的快速适应性活动,控制进食的神经回路具有由神经递质和激素调节的突触可塑性,这些神经递质和激素在不同的整合层次上发挥作用。在下丘脑中,在内源性大麻素(eCBs)参与这种整合的化学介质中,它们是神经元功能快速(即非基因组)、与应激相关的微调的理想候选者。在本文中,我们概述了内源性大麻素系统(ECS)在控制能量摄入,特别是在高能量、美味食物消费中的作用,并讨论了进食调节激素水平的变化,如脂肪组织衍生的厌食介质瘦素,以及高脂饮食如何在大脑中影响这种作用。对内源性大麻素对进食行为的神经元控制的分子机制的理解为对抗肥胖的新型治疗方法提供了许多潜在机会。本文还讨论了在“西方饮食”驱动的肥胖中尽量减少中枢ECS过度活动的策略的最新进展。