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大麻素和内源性大麻素系统在调节糖尿病性心肌病中的作用。

Role of cannabinoids and the endocannabinoid system in modulation of diabetic cardiomyopathy.

作者信息

El-Azab Mona F, Wakiel Ahmed E, Nafea Yossef K, Youssef Mahmoud E

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.

Program of Biochemistry, McMaster University, Hamilton L8S 4L8, Ontario, Canada.

出版信息

World J Diabetes. 2022 May 15;13(5):387-407. doi: 10.4239/wjd.v13.i5.387.

Abstract

Diabetic complications, chiefly seen in long-term situations, are persistently deleterious to a large extent, requiring multi-factorial risk reduction strategies beyond glycemic control. Diabetic cardiomyopathy is one of the most common deleterious diabetic complications, being the leading cause of mortality among diabetic patients. The mechanisms of diabetic cardiomyopathy are multi-factorial, involving increased oxidative stress, accumulation of advanced glycation end products (AGEs), activation of various pro-inflammatory and cell death signaling pathways, and changes in the composition of extracellular matrix with enhanced cardiac fibrosis. The novel lipid signaling system, the endocannabinoid system, has been implicated in the pathogenesis of diabetes and its complications through its two main receptors: Cannabinoid receptor type 1 and cannabinoid receptor type 2, alongside other components. However, the role of the endocannabinoid system in diabetic cardiomyopathy has not been fully investigated. This review aims to elucidate the possible mechanisms through which cannabinoids and the endocannabinoid system could interact with the pathogenesis and the development of diabetic cardiomyopathy. These mechanisms include oxidative/ nitrative stress, inflammation, accumulation of AGEs, cardiac remodeling, and autophagy. A better understanding of the role of cannabinoids and the endocannabinoid system in diabetic cardiomyopathy may provide novel strategies to manipulate such a serious diabetic complication.

摘要

糖尿病并发症主要见于长期患病情况,在很大程度上具有持续性危害,需要采取除血糖控制之外的多因素风险降低策略。糖尿病性心肌病是最常见的有害糖尿病并发症之一,是糖尿病患者死亡的主要原因。糖尿病性心肌病的机制是多因素的,包括氧化应激增加、晚期糖基化终产物(AGEs)积累、各种促炎和细胞死亡信号通路的激活,以及细胞外基质组成改变伴心脏纤维化增强。新型脂质信号系统——内源性大麻素系统,已通过其两个主要受体:1型大麻素受体和2型大麻素受体以及其他成分,参与糖尿病及其并发症的发病机制。然而,内源性大麻素系统在糖尿病性心肌病中的作用尚未得到充分研究。本综述旨在阐明大麻素和内源性大麻素系统可能与糖尿病性心肌病的发病机制和发展相互作用的机制。这些机制包括氧化/硝化应激、炎症、AGEs积累、心脏重塑和自噬。更好地理解大麻素和内源性大麻素系统在糖尿病性心肌病中的作用,可能为应对这种严重的糖尿病并发症提供新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944c/9134026/1311616778c9/WJD-13-387-g001.jpg

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