Simon Vincent, Cota Daniela
INSERM and University of BordeauxNeurocentre Magendie, Physiopathologie de la Plasticité Neuronale, U1215, Bordeaux, France.
Eur J Endocrinol. 2017 Jun;176(6):R309-R324. doi: 10.1530/EJE-16-1044. Epub 2017 Feb 28.
The endocannabinoid system (ECS), including cannabinoid type 1 and type 2 receptors (CBR and CBR), endogenous ligands called endocannabinoids and their related enzymatic machinery, is known to have a role in the regulation of energy balance. Past information generated on the ECS, mainly focused on the involvement of this system in the central nervous system regulation of food intake, while at the same time clinical studies pointed out the therapeutic efficacy of brain penetrant CBR antagonists like rimonabant for obesity and metabolic disorders. Rimonabant was removed from the market in 2009 and its obituary written due to its psychiatric side effects. However, in the meanwhile a number of investigations had started to highlight the roles of the peripheral ECS in the regulation of metabolism, bringing up new hope that the ECS might still represent target for treatment. Accordingly, peripherally restricted CBR antagonists or inverse agonists have shown to effectively reduce body weight, adiposity, insulin resistance and dyslipidemia in obese animal models. Very recent investigations have further expanded the possible toolbox for the modulation of the ECS, by demonstrating the existence of endogenous allosteric inhibitors of CBR, the characterization of the structure of the human CBR, and the likely involvement of CBR in metabolic disorders. Here we give an overview of these findings, discussing what the future may hold in the context of strategies targeting the ECS in metabolic disease.
内源性大麻素系统(ECS),包括1型和2型大麻素受体(CBR1和CBR2)、被称为内源性大麻素的内源性配体及其相关的酶机制,已知在能量平衡调节中发挥作用。过去关于ECS的信息主要集中在该系统参与中枢神经系统对食物摄入的调节,而与此同时,临床研究指出像利莫那班这样的可穿透血脑屏障的CBR1拮抗剂对肥胖和代谢紊乱具有治疗效果。利莫那班于2009年退市,因其精神方面的副作用而被停用。然而,在此期间,一些研究开始强调外周ECS在代谢调节中的作用,带来了新的希望,即ECS可能仍然是治疗靶点。相应地,外周选择性CBR1拮抗剂或反向激动剂已被证明能在肥胖动物模型中有效减轻体重、降低肥胖程度、改善胰岛素抵抗和血脂异常。最近的研究通过证实CBR1内源性变构抑制剂的存在、对人CBR1结构的表征以及CBR1可能参与代谢紊乱,进一步扩展了调节ECS的可能手段。在此,我们概述这些发现,并讨论在针对代谢疾病中ECS的策略背景下未来可能的发展方向。