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重新审视内源性大麻素系统及其在肥胖症和相关疾病中的治疗潜力。

Re-visiting the Endocannabinoid System and Its Therapeutic Potential in Obesity and Associated Diseases.

作者信息

Richey Joyce M, Woolcott Orison

机构信息

USC Diabetes and Obesity Research Institute, Keck School of Medicine of USC, 2250 Alcazar Street, Suite 213, Los Angeles, CA, 90089, USA.

Diabetes and Obesity Research Institute, Cedars-Sinai Medical Center, 8700 Beverly Blvd, Thalians E103, Los Angeles, CA, 90048, USA.

出版信息

Curr Diab Rep. 2017 Sep 14;17(10):99. doi: 10.1007/s11892-017-0924-x.

Abstract

PURPOSE OF REVIEW

The purpose of the review was to revisit the possibility of the endocannabinoid system being a therapeutic target for the treatment of obesity by focusing on the peripheral roles in regulating appetite and energy metabolism.

RECENT FINDINGS

Previous studies with the global cannabinoid receptor blocker rimonabant, which has both central and peripheral properties, showed that this drug has beneficial effects on cardiometabolic function but severe adverse psychiatric side effects. Consequently, focus has shifted to peripherally restricted cannabinoid 1 (CB1) receptor blockers as possible therapeutic agents that mitigate or eliminate the untoward effects in the central nervous system. Targeting the endocannabinoid system using novel peripheral CB1 receptor blockers with negligible penetrance across the blood-brain barrier may prove to be effective therapy for obesity and its co-morbidities. Perhaps the future of blockers targeting CB1 receptors will be tissue-specific neutral antagonists (e.g., skeletal muscle specific to treat peripheral insulin resistance, adipocyte-specific to treat fat excess, liver-specific to treat fatty liver and hepatic insulin resistance).

摘要

综述目的

本综述旨在重新审视内源性大麻素系统作为治疗肥胖症的治疗靶点的可能性,重点关注其在调节食欲和能量代谢方面的外周作用。

最新发现

先前使用兼具中枢和外周特性的全球大麻素受体阻滞剂利莫那班进行的研究表明,该药物对心脏代谢功能有有益作用,但存在严重的不良精神副作用。因此,研究重点已转向外周选择性大麻素1(CB1)受体阻滞剂,将其作为可能减轻或消除中枢神经系统不良影响的治疗药物。使用新型外周CB1受体阻滞剂靶向内源性大麻素系统,其透过血脑屏障的渗透率可忽略不计,这可能被证明是治疗肥胖症及其合并症的有效疗法。也许未来针对CB1受体的阻滞剂将是组织特异性中性拮抗剂(例如,针对治疗外周胰岛素抵抗的骨骼肌特异性拮抗剂、针对治疗脂肪过多的脂肪细胞特异性拮抗剂、针对治疗脂肪肝和肝脏胰岛素抵抗的肝脏特异性拮抗剂)。

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