粒体自噬
线粒体
寡霉素
抗霉素A
生物
药物发现
细胞生物学
化学
神经科学
生物化学
酶
自噬
细胞凋亡
ATP酶
作者
Sheikh Arslan Sehgal,Hao Wu,Sajid Muhammad,Summar Sohail,Muhammad Ahsan,Gulnaz Parveen,Mehreen Riaz,Muhammad Saleem Khan,Muhammad Nasir Iqbal,Abbeha Malik
出处
期刊:Current Neuropharmacology
[Bentham Science]
日期:2023-05-01
卷期号:21 (5): 1026-1041
被引量:3
标识
DOI:10.2174/1570159x21666230314140528
摘要
With the advancement in novel drug discovery, biologically active compounds are considered pharmacological tools to understand complex biological mechanisms and the identification of potent therapeutic agents. Mitochondria boast a central role in different integral biological processes and mitochondrial dysfunction is associated with multiple pathologies. It is, therefore, prudent to target mitochondrial quality control mechanisms by using pharmacological approaches. However, there is a scarcity of biologically active molecules, which can interact with mitochondria directly. Currently, the chemical compounds used to induce mitophagy include oligomycin and antimycin A for impaired respiration and acute dissipation of mitochondrial membrane potential by using CCCP/FCCP, the mitochondrial uncouplers. These chemical probes alter the homeostasis of the mitochondria and limit our understanding of the energy regulatory mechanisms. Efforts are underway to find molecules that can bring about selective removal of defective mitochondria without compromising normal mitochondrial respiration. In this report, we have tried to summarize and status of the recently reported modulators of mitophagy.
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