de Kloet Annette D, Woods Stephen C
Department of Psychiatry, University of Cincinnati, Cincinnati, Ohio 45237, USA.
Endocrinology. 2009 Jun;150(6):2531-6. doi: 10.1210/en.2009-0046. Epub 2009 Apr 16.
As the incidence of obesity continues to increase, the development of effective therapies is a high priority. The endocannabinoid system has emerged as an important influence on the regulation of energy homeostasis. The endocannabinoids anandamide and 2-arachidonoylglycerol act on cannabinoid receptor-1 (CB1) in the brain and many peripheral tissues causing a net anabolic action. This includes increasing food intake, and causing increased lipogenesis and fat storage in adipose tissue and liver. The endocannabinoid system is hyperactive in obese humans and animals, and treating them with CB1 antagonists causes weight loss and improved lipid and glucose profiles. Although clinical trials with CB1 antagonists have yielded beneficial metabolic effects, concerns about negative affect have limited the therapeutic potential of the first class of CB1 antagonists available.
随着肥胖症发病率持续上升,开发有效的治疗方法成为当务之急。内源性大麻素系统已成为能量稳态调节中的一个重要影响因素。内源性大麻素花生四烯乙醇胺和2-花生四烯酸甘油酯作用于大脑及许多外周组织中的大麻素受体-1(CB1),产生净合成代谢作用。这包括增加食物摄入量,以及导致脂肪组织和肝脏中脂肪生成增加和脂肪储存增加。内源性大麻素系统在肥胖的人类和动物中功能亢进,用CB1拮抗剂治疗他们会导致体重减轻,并改善脂质和葡萄糖状况。尽管使用CB1拮抗剂的临床试验已产生有益的代谢效应,但对负面影响的担忧限制了首批可用CB1拮抗剂的治疗潜力。