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A Mitochondrial-Targeted Nitroxide Is a Potent Inhibitor of Ferroptosis

机译:线粒体靶向的一氧化氮是一种强效的肥大病抑制剂

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Discovering compounds and mechanisms for inhibiting ferroptosis, a form of regulated, nonapoptotic cell death, has been of great interest in recent years. In this study, we demonstrate the ability of XJB-5-131, JP4-039, and other nitroxide-based lipid peroxidation mitigators to prevent ferroptotic cell death in HT-1080, BJeLR, and panc-1 cells. Several analogues of the reactive oxygen species (ROS) scavengers XJB-5-131 and JP4-039 were synthesized to probe structure–activity relationships and the influence of subcellular localization on the potency of these novel ferroptosis suppressors. Their biological activity correlated well over several orders of magnitude with their structure, relative lipophilicity, and respective enrichment in mitochondria, revealing a critical role of intramitochondrial lipid peroxidation in ferroptosis. These results also suggest that preventing mitochondrial lipid oxidation might offer a viable therapeutic opportunity in ischemia/reperfusion-induced tissue injury, acute kidney injury, and other pathologies that involve ferroptotic cell death pathways.
机译:近年来,发现抑制ferroptosis的化合物和机制,ferroptosis是一种受调节的非凋亡性细胞死亡的形式,引起了人们的极大兴趣。在这项研究中,我们证明了XJB-5-131,JP4-039和其他基于氮氧化物的脂质过氧化缓解剂能够防止HT-1080,BJeLR和panc-1细胞中肥大细胞死亡。合成了几种活性氧清除剂XJB-5-131和JP4-039的类似物,以探讨结构与活性之间的关系以及亚细胞定位对这些新型肥大化抑制因子效力的影响。它们的生物学活性与其结构,相对亲脂性和线粒体各自的富集程度在几个数量级上具有良好的相关性,揭示了线粒体内脂质过氧化在肥大症中的关键作用。这些结果还表明,预防线粒体脂质氧化可能在缺血/再灌注诱导的组织损伤,急性肾损伤和其他涉及肥大细胞死亡途径的病理中提供可行的治疗机会。

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