Shen Jingsong, Fu Hengsong, Ding Yanling, Yuan Ziyang, Xiang Zeming, Ding Miao, Huang Min, Peng Yongquan, Li Tao, Zha Kelan, Ye Qiang
Department of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
Key Laboratory of Medical Electrophysiology of Ministry of Education and Medical Electrophysiological Key Laboratory of Sichuan Province, Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Disease, Institute of Cardiovascular Research, Southwest Medical University, Luzhou 646000, China.
Int J Cardiol Heart Vasc. 2024 Apr 26;52:101414. doi: 10.1016/j.ijcha.2024.101414. eCollection 2024 Jun.
Ferroptosis is a newly discovered form of programmed cell death triggered by intracellular iron overload, which leads to the accumulation of lipid peroxides in various cells. It has been implicated in the pathogenesis and progression of various diseases, including tumors, neurological disorders, and cardiovascular diseases. The intricate mechanism underlying ferroptosis involves an imbalance between the oxidation and antioxidant systems, disturbances in iron metabolism, membrane lipid peroxidation, and dysregulation of amino acid metabolism. We highlight the key molecular mechanisms governing iron overload and ferroptosis, and discuss potential molecular pathways linking ferroptosis with arrhythmias.
铁死亡是一种新发现的程序性细胞死亡形式,由细胞内铁过载触发,导致各种细胞中脂质过氧化物的积累。它与包括肿瘤、神经疾病和心血管疾病在内的各种疾病的发病机制和进展有关。铁死亡背后复杂的机制涉及氧化和抗氧化系统之间的失衡、铁代谢紊乱、膜脂质过氧化以及氨基酸代谢失调。我们强调了控制铁过载和铁死亡的关键分子机制,并讨论了将铁死亡与心律失常联系起来的潜在分子途径。