Davis Stephen N, Perkins Jennifer M
Division of Diabetes, Endocrinology and Metabolism, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
Endocr Pract. 2007 Nov-Dec;13(7):790-804. doi: 10.4158/EP.13.7.790.
To review the role of the endogenous cannabinoid system (ECS) in the peripheral and central regulation of food intake, appetite, and energy storage and discuss the potential for the ECS to be an important target for lowering cardiovascular risk.
Materials used for this article were identified through a MEDLINE search of the pertinent literature (1975 to present), including English-language randomized controlled, prospective, cohort, review, and observational studies. We summarize the available experimental and clinical data.
The ECS is composed of two 7-transmembrane G protein-coupled cannabinoid receptor subtypes, CB1 and CB2, endogenous cannabinoid ligands (anandamide and 2-arachidonoylglycerol), and the enzymes that synthesize and break down the ligands. Understanding the role of the ECS in central and peripheral metabolic processes related to the regulation of food intake and energy balance as well as the endocrine role of excess adipose tissue, particularly visceral adipose tissue, and its promotion of global cardiometabolic risk has led to the development of pharmacologic agents with potential for blockade of CB1 receptors. In several studies, rimonabant (20 mg daily) demonstrated a favorable effect on various risk factors for cardiovascular disease, including dyslipidemia, abdominal obesity, insulin resistance, blood pressure, and measures of inflammation.
The ECS has been shown to have a key role in the regulation of energy balance, and modulation of this system may affect multiple cardiometabolic risk factors. Clinical studies involving pharmacologic blockade of CB1 receptors in overweight patients with and without type 2 diabetes have demonstrated effective weight loss and improvements in several risk factors for cardiovascular disease.
综述内源性大麻素系统(ECS)在食物摄入、食欲及能量储存的外周和中枢调节中的作用,并探讨ECS作为降低心血管风险重要靶点的潜力。
通过对MEDLINE中相关文献(1975年至今)进行检索来确定本文所用资料,包括英文的随机对照、前瞻性、队列、综述及观察性研究。我们总结了现有的实验和临床数据。
ECS由两种7次跨膜G蛋白偶联大麻素受体亚型CB1和CB2、内源性大麻素配体(花生四烯乙醇胺和2-花生四烯酸甘油酯)以及合成和分解这些配体的酶组成。了解ECS在与食物摄入和能量平衡调节相关的中枢和外周代谢过程中的作用,以及多余脂肪组织,特别是内脏脂肪组织的内分泌作用及其对整体心脏代谢风险的促进作用,已促使开发出具有阻断CB1受体潜力的药物。在多项研究中,利莫那班(每日20毫克)对心血管疾病的各种危险因素,包括血脂异常、腹部肥胖、胰岛素抵抗、血压及炎症指标,均显示出有益作用。
已证明ECS在能量平衡调节中起关键作用,调节该系统可能会影响多个心脏代谢危险因素。对患有和未患有2型糖尿病的超重患者进行的涉及CB1受体药物阻断的临床研究已证明可有效减轻体重并改善多种心血管疾病危险因素。