The molecular mechanism of ferroptosis and its relationship with Parkinson's disease

Neurodegenerative diseases such as Parkinson's disease (PD) have complex pathogenetic mechanisms. Genetic, age, and environmental factors are all related to PD. Due to the unclear pathogenesis of PD and the lack of effective cure methods, it is urgent to find new targets for treating PD patient...

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Veröffentlicht in:Brain research bulletin 2024-07, Vol.213, p.110991, Article 110991
Hauptverfasser: Su, Yan, Jiao, Yue, Cai, Sheng, Xu, Yang, Wang, Qi, Chen, Xianwen
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Sprache:eng
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Zusammenfassung:Neurodegenerative diseases such as Parkinson's disease (PD) have complex pathogenetic mechanisms. Genetic, age, and environmental factors are all related to PD. Due to the unclear pathogenesis of PD and the lack of effective cure methods, it is urgent to find new targets for treating PD patients. Ferroptosis is a form of cell death that is reliant on iron and exhibits distinct morphological and mechanistic characteristics compared to other types of cell death. It encompasses a range of biological processes, including iron/lipid metabolism and oxidative stress. In recent years, research has found that ferroptosis plays a crucial role in the pathophysiological processes of neurodegenerative diseases and stroke. Therefore, ferroptosis is also closely related to PD, This article reviews the core mechanisms of ferroptosis and elucidates the correlation between PD and ferroptosis. In addition, new compounds that have emerged in recent years to exert anti PD effects by inhibiting the ferroptosis signaling pathway were summarized. I hope to further elaborate the relationship between ferroptosis and PD through the review of this article, and provide new strategies for developing PD treatments targeting ferroptosis. •This article reviews the core mechanisms of ferroptosis and elucidates the correlation between PD and ferroptosis.•New compounds that have emerged in recent years to exert anti-PD effects by inhibiting the ferroptosis were summarized.•I hope to through this review provide new strategies for developing PD treatments targeting ferroptosis.
ISSN:0361-9230
1873-2747
1873-2747
DOI:10.1016/j.brainresbull.2024.110991