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内源性大麻素系统在肾脏疾病发病机制及治疗中的新作用。

The emerging role of the endocannabinoid system in the pathogenesis and treatment of kidney diseases.

作者信息

Tam Joseph

出版信息

J Basic Clin Physiol Pharmacol. 2016 May 1;27(3):267-76. doi: 10.1515/jbcpp-2015-0055.

DOI:10.1515/jbcpp-2015-0055
PMID:26280171
Abstract

Endocannabinoids (eCBs) are endogenous lipid ligands that bind to cannabinoid receptors that also mediate the effects of marijuana. The eCB system is comprised of eCBs, anandamide, and 2-arachidonoyl glycerol, their cannabinoid-1 and cannabinoid-2 receptors (CB1 and CB2, respectively), and the enzymes involved in their biosynthesis and degradation. It is present in both the central nervous system and peripheral organs including the kidney. The current review focuses on the role of the eCB system in normal kidney function and various diseases, such as diabetes and obesity, that directly contributes to the development of renal pathologies. Normally, activation of the CB1 receptor regulates renal vascular hemodynamics and stimulates the transport of ions and proteins in different nephron compartments. In various mouse and rat models of obesity and type 1 and 2 diabetes mellitus, eCBs generated in various renal cells activate CB1 receptors and contribute to the development of oxidative stress, inflammation, and renal fibrosis. These effects can be chronically ameliorated by CB1 receptor blockers. In contrast, activation of the renal CB2 receptors reduces the deleterious effects of these chronic diseases. Because the therapeutic potential of globally acting CB1 receptor antagonists in these conditions is limited due to their neuropsychiatric adverse effects, the recent development of peripherally restricted CB1 receptor antagonists may represent a novel pharmacological approach in treating renal diseases.

摘要

内源性大麻素(eCBs)是内源性脂质配体,可与大麻素受体结合,而大麻素受体也介导大麻的作用。eCB系统由eCBs、花生四烯乙醇胺和2-花生四烯酸甘油、它们的大麻素-1和大麻素-2受体(分别为CB1和CB2)以及参与其生物合成和降解的酶组成。它存在于中枢神经系统和包括肾脏在内的外周器官中。本综述重点关注eCB系统在正常肾功能以及各种疾病(如糖尿病和肥胖症)中的作用,这些疾病直接促成了肾脏病变的发展。正常情况下,CB1受体的激活调节肾血管血流动力学,并刺激不同肾单位区域的离子和蛋白质转运。在各种肥胖症以及1型和2型糖尿病的小鼠和大鼠模型中,各种肾细胞中产生的eCBs激活CB1受体,并促成氧化应激、炎症和肾纤维化的发展。这些作用可通过CB1受体阻滞剂长期改善。相比之下,肾CB2受体的激活可减轻这些慢性疾病的有害影响。由于全身性作用的CB1受体拮抗剂在这些情况下的治疗潜力因其神经精神不良反应而受到限制,因此最近开发的外周限制性CB1受体拮抗剂可能代表了一种治疗肾脏疾病的新型药理学方法。

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