Jin Eun-Ju, Jo Yunju, Wei Shibo, Rizzo Manfredi, Ryu Dongryeol, Gariani Karim
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, Republic of Korea.
College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Front Endocrinol (Lausanne). 2024 Aug 30;15:1447148. doi: 10.3389/fendo.2024.1447148. eCollection 2024.
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.
糖尿病是一种复杂的慢性疾病,被认为是全球最常见的代谢紊乱之一,对全球公共卫生构成重大威胁。铁死亡作为一种新型的程序性细胞死亡机制出现,不同于凋亡、坏死和自噬,由铁依赖性脂质过氧化积累和谷胱甘肽过氧化物酶4(GPx4)下调驱动。越来越多的证据强调了铁代谢、铁死亡与糖尿病发病机制之间的相互联系,包括糖尿病肾病、心肌病和神经病变等并发症。此外,铁死亡抑制剂有望成为减轻糖尿病相关并发症的潜在药理学靶点。更好地理解铁死亡在糖尿病中的作用可能会改善全球糖尿病的管理。在本综述中,我们深入探讨铁死亡与糖尿病发展之间的复杂关系,探索相关并发症和当前的药物治疗方法。