自噬
神经保护
程序性细胞死亡
神经科学
粒体自噬
细胞生物学
生物
机制(生物学)
缺血
冲程(发动机)
医学
细胞凋亡
生物化学
内科学
工程类
哲学
认识论
机械工程
作者
Seyed Fazel Nabavi,Antoni Sureda,A. Sanches‐Silva,Kasi Pandima Devi,Touqeer Ahmed,Momina Shahid,Eduardo Sobarzo‐Sánchez,Marco Dacrema,Maria Daglia,Nady Braidy,Rosa Anna Vacca,Ioana Berindan‐Neagoe,Diana Gulei,Davide Barreca,Maciej Banach,Seyed Mohammad Nabavi,Ahmad Reza Dehpour,Samira Shirooie
标识
DOI:10.1080/10408363.2019.1575333
摘要
Autophagy is an important biological mechanism involved in the regulation of numerous fundamental cellular processes that are mainly associated with cellular growth and differentiation. Autophagic pathways are vital for maintaining cellular homeostasis by enhancing the turnover of nonfunctional proteins and organelles. Neuronal cells, like other eukaryotic cells, are dependent on autophagy for neuroprotection in response to stress, but can also induce cell death in cerebral ischemia. Recent studies have demonstrated that autophagy may induce neuroprotection following acute brain injury, including ischemic stroke. However in some special circumstances, activation of autophagy can induce cell death, playing a deleterious role in the etiology and progression of ischemic stroke. Currently, there are no therapeutic options against stroke that demonstrate efficient neuroprotective abilities. In the present work, we will review the significance of autophagy in the context of ischemic stroke by first outlining its role in ischemic neuronal death. We will also highlight the potential therapeutic applications of pharmacological modulators of autophagy, including some naturally occurring polyphenolic compounds that can target this catabolic process. Our findings provide renewed insight on the mechanism of action of autophagy in stroke together with potential neuroprotective compounds, which may partially exert their function through enhancing mitochondrial function and attenuating damaging autophagic processes.
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