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内源性大麻素与体重控制

Endocannabinoids in Body Weight Control.

作者信息

Horn Henrike, Böhme Beatrice, Dietrich Laura, Koch Marco

机构信息

Institute of Anatomy, Medical Faculty, University of Leipzig, 04103 Leipzig, Germany.

出版信息

Pharmaceuticals (Basel). 2018 May 30;11(2):55. doi: 10.3390/ph11020055.

Abstract

Maintenance of body weight is fundamental to maintain one's health and to promote longevity. Nevertheless, it appears that the global obesity epidemic is still constantly increasing. Endocannabinoids (eCBs) are lipid messengers that are involved in overall body weight control by interfering with manifold central and peripheral regulatory circuits that orchestrate energy homeostasis. Initially, blocking of eCB signaling by first generation cannabinoid type 1 receptor (CB1) inverse agonists such as rimonabant revealed body weight-reducing effects in laboratory animals and men. Unfortunately, rimonabant also induced severe psychiatric side effects. At this point, it became clear that future cannabinoid research has to decipher more precisely the underlying central and peripheral mechanisms behind eCB-driven control of feeding behavior and whole body energy metabolism. Here, we will summarize the most recent advances in understanding how central eCBs interfere with circuits in the brain that control food intake and energy expenditure. Next, we will focus on how peripheral eCBs affect food digestion, nutrient transformation and energy expenditure by interfering with signaling cascades in the gastrointestinal tract, liver, pancreas, fat depots and endocrine glands. To finally outline the safe future potential of cannabinoids as medicines, our overall goal is to address the molecular, cellular and pharmacological logic behind central and peripheral eCB-mediated body weight control, and to figure out how these precise mechanistic insights are currently transferred into the development of next generation cannabinoid medicines displaying clearly improved safety profiles, such as significantly reduced side effects.

摘要

维持体重对于保持健康和促进长寿至关重要。然而,全球肥胖流行似乎仍在持续加剧。内源性大麻素(eCBs)是脂质信使,通过干扰协调能量稳态的多种中枢和外周调节回路来参与总体体重控制。最初,第一代大麻素1型受体(CB1)反向激动剂如利莫那班阻断eCB信号传导,在实验动物和人类中显示出体重减轻的效果。不幸的是,利莫那班也引发了严重的精神副作用。此时,很明显未来的大麻素研究必须更精确地解读eCB驱动的进食行为和全身能量代谢背后的潜在中枢和外周机制。在此,我们将总结在理解中枢eCB如何干扰大脑中控制食物摄入和能量消耗的回路方面的最新进展。接下来,我们将关注外周eCB如何通过干扰胃肠道、肝脏、胰腺、脂肪库和内分泌腺中的信号级联反应来影响食物消化、营养转化和能量消耗。为了最终概述大麻素作为药物的安全未来潜力,我们的总体目标是阐述中枢和外周eCB介导的体重控制背后的分子、细胞和药理学逻辑,并弄清楚这些精确的机制见解目前如何转化为开发具有明显改善的安全性特征(如显著减少副作用)的下一代大麻素药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef70/6027162/2b5c77538d0a/pharmaceuticals-11-00055-g001.jpg

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