Departamento de Nutricion y Cultura Fisica, Centro de Ciencias de la Salud, Universidad Autonoma de Aguascalientes, Ciudad Universitaria, 20131 Aguascalientes, Ags, Mexico.
Departamento de Fisiologia, Facultad de Medicina. Universidad Nacional Autonoma de Mexico, Ciudad de Mexico, Mexico.
Curr Neuropharmacol. 2019;17(10):947-960. doi: 10.2174/1570159X17666190118143014.
Endocannabinoids are ancient biomolecules involved in several cellular (e.g., metabolism) and physiological (e.g., eating behaviour) functions. Indeed, eating behaviour alterations in marijuana users have led to investigate the orexigenic/anorexigenic effects of cannabinoids in animal/ human models. This increasing body of research suggests that the endocannabinoid system plays an important role in feeding control. Accordingly, within the endocannabinoid system, cannabinoid receptors, enzymes and genes represent potential therapeutic targets for dealing with multiple metabolic and behavioural dysfunctions (e.g., obesity, anorexia, etc.). Paradoxically, our understanding on the endocannabinoid system as a cellular mediator is yet limited. For example: (i) only two cannabinoid receptors have been classified, but they are not enough to explain the pharmacological profile of several experimental effects induced by cannabinoids; and (ii) several orphan G protein-coupled receptors (GPCRs) interact with cannabinoids and we do not know how to classify them (e.g., GPR18, GPR55 and GPR119; amongst others). On this basis, the present review attempts to summarize the lines of evidence supporting the potential role of GPR18, GPR55 and GPR119 in metabolism and feeding control that may explain some of the divergent effects and puzzling data related to cannabinoid research. Moreover, their therapeutic potential in feeding behaviour alterations will be considered.
内源性大麻素是参与多种细胞(如代谢)和生理(如进食行为)功能的古老生物分子。事实上,大麻使用者的进食行为改变导致人们在动物/人类模型中研究大麻素的食欲刺激/厌食作用。越来越多的研究表明,内源性大麻素系统在进食控制中发挥着重要作用。因此,在内源性大麻素系统中,大麻素受体、酶和基因代表了治疗多种代谢和行为功能障碍(如肥胖、厌食等)的潜在治疗靶点。矛盾的是,我们对内源性大麻素系统作为细胞介质的理解还很有限。例如:(i)仅分类了两种大麻素受体,但它们不足以解释大麻素引起的几种实验效应的药理学特征;(ii)几种孤儿 G 蛋白偶联受体(GPCR)与大麻素相互作用,我们不知道如何对它们进行分类(例如,GPR18、GPR55 和 GPR119;等等)。在此基础上,本综述试图总结支持 GPR18、GPR55 和 GPR119 在代谢和进食控制中发挥潜在作用的证据,这可能解释了与大麻素研究相关的一些不同作用和令人困惑的数据。此外,还将考虑它们在进食行为改变中的治疗潜力。