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铁死亡与心肌缺血再灌注损伤中线粒体自噬的关系:小型综述。

Relationship between ferroptosis and mitophagy in cardiac ischemia reperfusion injury: a mini-review.

机构信息

Third-Grade Pharmacological Laboratory on Traditional Chinese Medicine, State Administration of Traditional Chinese Medicine, Medical College, China Three Gorges University, Yichang, Hubei Province, China.

The Second Clinical College of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong Province, China.

出版信息

PeerJ. 2023 Mar 13;11:e14952. doi: 10.7717/peerj.14952. eCollection 2023.

Abstract

Cardiovascular diseases (CVD), with high morbidity and mortality, seriously affect people's life and social development. Clinically, reperfusion therapy is typically used to treat ischemic cardiomyopathy, such as severe coronary heart disease and acute myocardial infarction. However, reperfusion therapy can lead to myocardial ischemia reperfusion injury (MIRI), which can affect the prognosis of patients. Studying the mechanisms of MIRI can help us improve the treatment of MIRI. The pathological process of MIRI involves many mechanisms such as ferroptosis and mitophagy. Ferroptosis can exacerbate MIRI, and regulation of mitophagy can alleviate MIRI. Both ferroptosis and mitophagy are closely related to ROS, but there is no clear understanding of the relationship between ferroptosis and mitophagy. In this review, we analyzed the relationship between ferroptosis and mitophagy according to the role of mTOR, NLPR3 and HIF. In addition, simultaneous regulation of mitophagy and ferroptosis may be superior to single therapy for MIRI. We summarized potential drugs that can regulate mitophagy and/or ferroptosis, hoping to provide reference for the development of drugs and methods for MIRI treatment.

摘要

心血管疾病(CVD)发病率和死亡率高,严重影响人们的生活和社会发展。临床上,再灌注治疗通常用于治疗缺血性心肌病,如严重的冠心病和急性心肌梗死。然而,再灌注治疗可导致心肌缺血再灌注损伤(MIRI),从而影响患者的预后。研究 MIRI 的机制有助于我们改善 MIRI 的治疗。MIRI 的病理过程涉及许多机制,如铁死亡和线粒体自噬。铁死亡会加重 MIRI,而调节线粒体自噬可以减轻 MIRI。铁死亡和线粒体自噬都与 ROS 密切相关,但铁死亡和线粒体自噬之间的关系尚不清楚。在本综述中,我们根据 mTOR、NLPR3 和 HIF 的作用分析了铁死亡和线粒体自噬之间的关系。此外,线粒体自噬和铁死亡的同时调节可能优于 MIRI 的单一治疗。我们总结了可能调节线粒体自噬和/或铁死亡的潜在药物,希望为 MIRI 治疗的药物和方法的发展提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/489f/10019339/9e7c64540d6c/peerj-11-14952-g001.jpg

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