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针对糖尿病性心肌病的线粒体质量控制:降糖药物的治疗潜力。

Targeting mitochondrial quality control for diabetic cardiomyopathy: Therapeutic potential of hypoglycemic drugs.

机构信息

Guang'an Men Hospital, China Academy of Chinese Medicine, Beijing 100053, China.

LongHua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China.

出版信息

Biomed Pharmacother. 2023 Dec;168:115669. doi: 10.1016/j.biopha.2023.115669. Epub 2023 Oct 9.

Abstract

Diabetic cardiomyopathy is a chronic cardiovascular complication caused by diabetes that is characterized by changes in myocardial structure and function, ultimately leading to heart failure and even death. Mitochondria serve as the provider of energy to cardiomyocytes, and mitochondrial dysfunction plays a central role in the development of diabetic cardiomyopathy. In response to a series of pathological changes caused by mitochondrial dysfunction, the mitochondrial quality control system is activated. The mitochondrial quality control system (including mitochondrial biogenesis, fusion and fission, and mitophagy) is core to maintaining the normal structure of mitochondria and performing their normal physiological functions. However, mitochondrial quality control is abnormal in diabetic cardiomyopathy, resulting in insufficient mitochondrial fusion and excessive fission within the cardiomyocyte, and fragmented mitochondria are not phagocytosed in a timely manner, accumulating within the cardiomyocyte resulting in cardiomyocyte injury. Currently, there is no specific therapy or prevention for diabetic cardiomyopathy, and glycemic control remains the mainstay. In this review, we first elucidate the pathogenesis of diabetic cardiomyopathy and explore the link between pathological mitochondrial quality control and the development of diabetic cardiomyopathy. Then, we summarize how clinically used hypoglycemic agents (including sodium-glucose cotransport protein 2 inhibitions, glucagon-like peptide-1 receptor agonists, dipeptidyl peptidase-4 inhibitors, thiazolidinediones, metformin, and α-glucosidase inhibitors) exert cardioprotective effects to treat and prevent diabetic cardiomyopathy by targeting the mitochondrial quality control system. In addition, the mechanisms of complementary alternative therapies, such as active ingredients of traditional Chinese medicine, exercise, and lifestyle, targeting mitochondrial quality control for the treatment of diabetic cardiomyopathy are also added, which lays the foundation for the excavation of new diabetic cardioprotective drugs.

摘要

糖尿病心肌病是一种由糖尿病引起的慢性心血管并发症,其特征是心肌结构和功能发生变化,最终导致心力衰竭甚至死亡。线粒体为心肌细胞提供能量,线粒体功能障碍在糖尿病心肌病的发生发展中起核心作用。针对线粒体功能障碍引起的一系列病理变化,线粒体质量控制系统被激活。线粒体质量控制系统(包括线粒体生物发生、融合和裂变、以及自噬)是维持线粒体正常结构和发挥正常生理功能的核心。然而,在糖尿病心肌病中,线粒体质量控制异常,导致心肌细胞内线粒体融合不足而裂变过度,且碎裂的线粒体不能及时被吞噬,在心肌细胞内堆积,导致心肌细胞损伤。目前,糖尿病心肌病尚无特异性治疗或预防方法,血糖控制仍然是主要方法。在这篇综述中,我们首先阐明了糖尿病心肌病的发病机制,并探讨了病理性线粒体质量控制与糖尿病心肌病发生发展之间的联系。然后,我们总结了临床上使用的降糖药物(包括钠-葡萄糖共转运蛋白 2 抑制剂、胰高血糖素样肽-1 受体激动剂、二肽基肽酶-4 抑制剂、噻唑烷二酮类、二甲双胍和α-葡萄糖苷酶抑制剂)通过靶向线粒体质量控制系统发挥心脏保护作用来治疗和预防糖尿病心肌病的作用机制。此外,还增加了针对线粒体质量控制治疗糖尿病心肌病的补充替代疗法(如中药活性成分、运动和生活方式)的机制,为挖掘新的糖尿病心脏保护药物奠定了基础。

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