糖尿病
医学
发病机制
自噬
疾病
GPX4
糖尿病性心肌病
生物信息学
机制(生物学)
细胞凋亡
心肌病
免疫学
内科学
内分泌学
生物
氧化应激
心力衰竭
遗传学
认识论
哲学
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Eun‐Ju Jin,Yunju Jo,Shibo Wei,Manfredi Rizzo,Dongryeol Ryu,Karim Gariani
标识
DOI:10.3389/fendo.2024.1447148
摘要
Diabetes mellitus is a complex chronic disease, considered as one of the most common metabolic disorders worldwide, posing a major threat to global public health. Ferroptosis emerges as a novel mechanism of programmed cell death, distinct from apoptosis, necrosis, and autophagy, driven by iron-dependent lipid peroxidation accumulation and GPx4 downregulation. A mounting body of evidence highlights the interconnection between iron metabolism, ferroptosis, and diabetes pathogenesis, encompassing complications like diabetic nephropathy, cardiomyopathy, and neuropathy. Moreover, ferroptosis inhibitors hold promise as potential pharmacological targets for mitigating diabetes-related complications. A better understanding of the role of ferroptosis in diabetes may lead to an improvement in global diabetes management. In this review, we delve into the intricate relationship between ferroptosis and diabetes development, exploring associated complications and current pharmacological treatments.
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