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Relationship between oxidative stress and nuclear factor-erythroid-2-related factor 2 signaling in diabetic cardiomyopathy (Review)

期刊

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/etm.2021.10110

关键词

cardiac diseases; oxidative stress; nuclear factor-erythroid-2-related factor 2; antioxidant response element; diabetic cardiomyopathy; Kelch-like ECH-associated protein 1

资金

  1. National Natural Science Foundation of China [00019509]
  2. Jiangxi Provincial Natural Science Foundation [700207006]

向作者/读者索取更多资源

Diabetic cardiomyopathy is a major cause of death worldwide, with oxidative stress playing a key role in its pathophysiology. NRF2 is a transcription factor that regulates antioxidant gene expression and detoxifying enzymes, helping to maintain cardiac homeostasis and counteract oxidative stress. Targeting the NRF2 signaling pathway may be a potential strategy for preventing and treating DCM and other cardiac diseases.
Diabetic cardiomyopathy (DCM) is the leading cause of death worldwide, and oxidative stress was discovered to serve an important role in the pathophysiology of the condition. An imbalance between free radicals and antioxidant defenses is known to be associated with cellular dysfunction, leading to the development of various types of cardiac disease. Nuclear factor-erythroid-2-related factor 2 (NRF2) is a transcription factor that controls the basal and inducible expression levels of various antioxidant genes and other cytoprotective phase II detoxifying enzymes, which are ubiquitously expressed in the cardiac system. Kelch-like ECH-associated protein 1 (Keap1) serves as the main intracellular regulator of NRF2. Emerging evidence has revealed that NRF2 is a critical regulator of cardiac homeostasis via the suppression of oxidative stress. The activation of NRF2 was discovered to enhance specific endogenous antioxidant defense factors, one of which is antioxidant response element (ARE), which was subsequently illustrated to detoxify and counteract oxidative stress-associated DCM. The NRF2 signaling pathway is closely associated with the development of various types of cardiac disease, including ischemic heart disease, heart failure, myocardial infarction, atrial fibrillation and myocarditis. Therefore, it is hypothesized that drugs targeting this pathway may be developed to inhibit the activation of NRF2 signaling, thereby preventing the occurrence of DCM and effectively treating the disease.

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