Matias Isabel, Di Marzo Vincenzo
Endocannabinoid Research Group, Institute of Biomolecular Chemistry, Consiglio Nazionale delle Ricerche, via Campi Flegrei 34, 80078 Pozzuoli (Napoli), Italy.
Trends Endocrinol Metab. 2007 Jan-Feb;18(1):27-37. doi: 10.1016/j.tem.2006.11.006. Epub 2006 Dec 1.
Two receptors have been cloned to date for the psychotropic compound Delta(9)-tetrahydrocannabinol, and termed cannabinoid CB(1) and CB(2) receptors. Their endogenous ligands, the endocannabinoids, have also been identified. CB(1) receptors and endocannabinoids are present in brain structures controlling energy intake and in peripheral cells (hepatocytes, adipocytes, pancreatic islet cells) regulating energy homeostasis. CB(2) receptors are more abundant in lymphocytes and macrophages, and participate in immune and inflammatory reactions. Metabolic hormones and peptides regulate the levels of the endocannabinoids and, hence, the activity of cannabinoid receptors in several tissues in a seemingly coordinated way. The endocannabinoids, particularly after stress and brief food deprivation, act in turn as local modulators of the expression and action of neurotransmitters, hormones and adipokines involved in metabolic control. Endocannabinoid overactivity seems to accompany metabolic and eating disorders and to contribute to the development of abdominal obesity, dyslipidemia and hyperglycemia. Accordingly, clinical trials have shown that CB(1) receptor antagonists are efficacious at reducing not only food intake, but also abdominal adiposity and its metabolic sequelae.
迄今为止,已克隆出两种与精神活性化合物Δ⁹-四氢大麻酚相关的受体,分别称为大麻素CB(1)和CB(2)受体。它们的内源性配体,即内源性大麻素,也已被鉴定出来。CB(1)受体和内源性大麻素存在于控制能量摄入的脑结构以及调节能量稳态的外周细胞(肝细胞、脂肪细胞、胰岛细胞)中。CB(2)受体在淋巴细胞和巨噬细胞中更为丰富,并参与免疫和炎症反应。代谢激素和肽以一种看似协调的方式调节内源性大麻素的水平,进而调节几种组织中大麻素受体的活性。内源性大麻素,尤其是在应激和短期食物剥夺后,反过来作为参与代谢控制的神经递质、激素和脂肪因子表达及作用的局部调节剂。内源性大麻素活性过高似乎与代谢和饮食紊乱相伴,并导致腹部肥胖、血脂异常和高血糖的发展。因此,临床试验表明,CB(1)受体拮抗剂不仅在减少食物摄入方面有效,而且在减少腹部肥胖及其代谢后遗症方面也有效。