Mitophagy in the Pathogenesis of Obesity-Associated Cardiovascular Diseases: New Mechanistic and Therapeutic Insights
Received 11 Apr, 2024 |
Accepted 18 May, 2024 |
Published 20 May, 2024 |
Mitophagy, a crucial mechanism for maintaining mitochondrial quality, involves the selective removal of damaged and potentially harmful mitochondria through autophagy. Despite its importance, the detailed mechanisms of mitophagy in the heart remain elusive. This review aims to explore the intricacies and therapeutic implications of mitophagy, particularly in the context of obesity, shedding light on its role in preserving cardiac function and cellular homeostasis. This review delves into three main mitophagy pathways: PINK1-PRKN, BNIP3/NIX and FUNDC1-mediated mitophagy. Additionally, this study analyze how obesity affects mitochondrial dynamics and subsequently contributes to cardiac dysfunction. Furthermore, current study discusses potential therapeutic strategies targeting mitophagy to mitigate cardiovascular diseases, hoping to offer new insights into potential therapeutic strategies.
How to Cite this paper?
APA-7 Style
Huang,
K., Ren,
J. (2024). Mitophagy in the Pathogenesis of Obesity-Associated Cardiovascular Diseases: New Mechanistic and Therapeutic Insights. Trends in Medical Research, 19(1), 112-123. https://doi.org/10.3923/tmr.2024.112.123
ACS Style
Huang,
K.; Ren,
J. Mitophagy in the Pathogenesis of Obesity-Associated Cardiovascular Diseases: New Mechanistic and Therapeutic Insights. Trends Med. Res 2024, 19, 112-123. https://doi.org/10.3923/tmr.2024.112.123
AMA Style
Huang
K, Ren
J. Mitophagy in the Pathogenesis of Obesity-Associated Cardiovascular Diseases: New Mechanistic and Therapeutic Insights. Trends in Medical Research. 2024; 19(1): 112-123. https://doi.org/10.3923/tmr.2024.112.123
Chicago/Turabian Style
Huang, Kexin, and Jun Ren.
2024. "Mitophagy in the Pathogenesis of Obesity-Associated Cardiovascular Diseases: New Mechanistic and Therapeutic Insights" Trends in Medical Research 19, no. 1: 112-123. https://doi.org/10.3923/tmr.2024.112.123
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