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不同的设计二胺促进线粒体自噬,从而延长 和 的寿命并保护人类细胞免受氧化损伤。

Distinct designer diamines promote mitophagy, and thereby enhance healthspan in and protect human cells against oxidative damage.

机构信息

Department Biochemistry and Molecular Biology, IMRIC, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.

Department Developmental Biology and Cancer Research, IMRIC, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.

出版信息

Autophagy. 2023 Feb;19(2):474-504. doi: 10.1080/15548627.2022.2078069. Epub 2022 Jun 1.

Abstract

Impaired mitophagy is a primary pathogenic event underlying diverse aging-associated diseases such as Alzheimer and Parkinson diseases and sarcopenia. Therefore, augmentation of mitophagy, the process by which defective mitochondria are removed, then replaced by new ones, is an emerging strategy for preventing the evolvement of multiple morbidities in the elderly population. Based on the scaffold of spermidine (Spd), a known mitophagy-promoting agent, we designed and tested a family of structurally related compounds. A prototypic member, 1,8-diaminooctane (VL-004), exceeds Spd in its ability to induce mitophagy and protect against oxidative stress. VL-004 activity is mediated by canonical aging genes and promotes lifespan and healthspan in . Moreover, it enhances mitophagy and protects against oxidative injury in rodent and human cells. Initial structural characterization suggests simple rules for the design of compounds with improved bioactivity, opening the way for a new generation of agents with a potential to promote healthy aging.

摘要

线粒体自噬受损是多种与衰老相关疾病(如阿尔茨海默病和帕金森病以及肌肉减少症)的主要致病事件。因此,增强线粒体自噬(即清除有缺陷的线粒体并由新的线粒体取代的过程)是预防老年人群多种疾病发展的一种新兴策略。基于精脒(Spd)的支架,一种已知的促进线粒体自噬的试剂,我们设计并测试了一系列结构相关的化合物。原型成员 1,8-二氨基辛烷(VL-004)在诱导线粒体自噬和抵抗氧化应激方面优于 Spd。VL-004 的活性是通过典型的衰老基因介导的,并能延长秀丽隐杆线虫的寿命和健康寿命。此外,它还能增强线粒体自噬并防止啮齿动物和人类细胞的氧化损伤。初步的结构特征表明,设计具有更高生物活性的化合物有简单的规则可循,为新一代具有促进健康衰老潜力的试剂开辟了道路。

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