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再探内源性大麻素拮抗剂:我们能否有选择性地针对外周组织来安全治疗肥胖和 2 型糖尿病?

Rehashing endocannabinoid antagonists: can we selectively target the periphery to safely treat obesity and type 2 diabetes?

机构信息

Joslin Diabetes Center and Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

J Clin Invest. 2010 Aug;120(8):2646-8. doi: 10.1172/JCI44099. Epub 2010 Jul 26.

Abstract

A growing body of evidence supports an important role for the endocannabinoid system as a regulator of appetite, body weight, and systemic metabolism, which is overactive in obesity and type 2 diabetes. While initial attempts to target this system using the cannabinoid receptor inverse agonist rimonabant were successful in producing modest weight loss and improving obesity-related metabolic complications in humans, adverse central nervous system side effects precluded introduction of this drug into clinical practice. However, new data, presented by Tam and colleagues in this issue of the JCI, demonstrate that selective blockade of peripheral cannabinoid receptors may be a novel successful therapeutic approach.

摘要

越来越多的证据表明,内源性大麻素系统作为食欲、体重和全身代谢的调节剂具有重要作用,而该系统在肥胖症和 2 型糖尿病中过度活跃。虽然最初尝试使用大麻素受体反向激动剂利莫那班来靶向该系统在人类中产生适度的体重减轻和改善肥胖相关代谢并发症方面取得了成功,但该药物因中枢神经系统不良反应而被排除在临床实践之外。然而,Tam 及其同事在本期《临床检查杂志》上发表的新数据表明,选择性阻断外周大麻素受体可能是一种新的成功的治疗方法。

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本文引用的文献

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Best Pract Res Clin Endocrinol Metab. 2009 Feb;23(1):87-102. doi: 10.1016/j.beem.2008.10.012.
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