老化
细胞代谢
脂质代谢
新陈代谢
程序性细胞死亡
机制(生物学)
细胞代谢
医学
肌萎缩
肥胖
生物
神经科学
细胞生物学
生物化学
内分泌学
遗传学
细胞凋亡
哲学
认识论
作者
Negin Kordi,Ali Saydi,Sajad Karami,Behnam Bagherzadeh-Rahmani,Emanuele Marzetti,F. Jung,Brent R. Stockwell
摘要
Ferroptosis is a form of programmed cell death that plays a significant role in causing several diseases such as heart attack and heart failure, through alterations in fat, amino acid, and iron metabolism. Comprehending the regulatory mechanisms of ferroptosis signaling is critical because it has a considerable effect on the elderly’s mortality. Conversely, age-related changes in substrate metabolism and metabolite levels are recognized to give rise to obesity. Furthermore, research has proposed that aging and obesity-related changes in substrate metabolism may aggravate ferroptosis. The suppression of ferroptosis holds potential as a successful therapeutic approach for managing different diseases, including sarcopenia, cardiovascular diseases, and central nervous system diseases. However, the pathologic and biological mechanisms behind the function of ferroptosis are not fully comprehended yet. Physical activity could affect lipid, amino acid, and iron metabolism to modulate ferroptosis. The aim of this study is to showcase the current understanding of the molecular mechanisms leading to ferroptosis and discuss the role of aging and physical activity in this phenomenon.
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