A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusion

Cerebral ischemia is one of the leading causes of death and disability worldwide. Although revascularization via reperfusion combined with advanced anticoagulant therapy is currently a gold standard treatment for patients, the reperfusion itself also results in a serious dysfunction termed cerebral...

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Main Authors: Yingying Tang, Jiaqian Xie, Xiaoping Chen, Lihong Sun, Lili Xu, Xinzhong Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-11-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2022.1040182/full
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author Yingying Tang
Jiaqian Xie
Xiaoping Chen
Lihong Sun
Lili Xu
Xinzhong Chen
author_facet Yingying Tang
Jiaqian Xie
Xiaoping Chen
Lihong Sun
Lili Xu
Xinzhong Chen
author_sort Yingying Tang
collection DOAJ
description Cerebral ischemia is one of the leading causes of death and disability worldwide. Although revascularization via reperfusion combined with advanced anticoagulant therapy is currently a gold standard treatment for patients, the reperfusion itself also results in a serious dysfunction termed cerebral ischemia-reperfusion (I/R) injury. Silent information regulator 1 (sirtuin 1, SIRT1), is a classic NAD+-dependent deacetylase, which has been proposed as an important mediator in the alleviation of cerebral ischemia through modulating multiple physiological processes, including apoptosis, inflammation, DNA repair, oxidative stress, and autophagy. Recent growing evidence suggests that SIRT1-mediated autophagy plays a key role in the pathophysiological process of cerebral I/R injury. SIRT1 could both activate and inhibit the autophagy process by mediating different autophagy pathways, such as the SIRT1-FOXOs pathway, SIRT1-AMPK pathway, and SIRT1-p53 pathway. However, the autophagic roles of SIRT1 in cerebral I/R injury have not been systematically summarized. Here, in this review, we will first introduce the molecular mechanisms and effects of SIRT1 in cerebral ischemia and I/R injury. Next, we will discuss the involvement of autophagy in the pathogenesis of cerebral I/R injury. Finally, we will summarize the latest advances in the interaction between SIRT1 and autophagy in cerebral I/R injury. A good understanding of these relationships would serve to consolidate a framework of mechanisms underlying SIRT1’s neuroprotective effects and provides evidence for the development of drugs targeting SIRT1.
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spelling doaj.art-294d4c93888b4f2fa3a95d981dd95d622022-12-22T03:43:46ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2022-11-011610.3389/fnins.2022.10401821040182A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusionYingying TangJiaqian XieXiaoping ChenLihong SunLili XuXinzhong ChenCerebral ischemia is one of the leading causes of death and disability worldwide. Although revascularization via reperfusion combined with advanced anticoagulant therapy is currently a gold standard treatment for patients, the reperfusion itself also results in a serious dysfunction termed cerebral ischemia-reperfusion (I/R) injury. Silent information regulator 1 (sirtuin 1, SIRT1), is a classic NAD+-dependent deacetylase, which has been proposed as an important mediator in the alleviation of cerebral ischemia through modulating multiple physiological processes, including apoptosis, inflammation, DNA repair, oxidative stress, and autophagy. Recent growing evidence suggests that SIRT1-mediated autophagy plays a key role in the pathophysiological process of cerebral I/R injury. SIRT1 could both activate and inhibit the autophagy process by mediating different autophagy pathways, such as the SIRT1-FOXOs pathway, SIRT1-AMPK pathway, and SIRT1-p53 pathway. However, the autophagic roles of SIRT1 in cerebral I/R injury have not been systematically summarized. Here, in this review, we will first introduce the molecular mechanisms and effects of SIRT1 in cerebral ischemia and I/R injury. Next, we will discuss the involvement of autophagy in the pathogenesis of cerebral I/R injury. Finally, we will summarize the latest advances in the interaction between SIRT1 and autophagy in cerebral I/R injury. A good understanding of these relationships would serve to consolidate a framework of mechanisms underlying SIRT1’s neuroprotective effects and provides evidence for the development of drugs targeting SIRT1.https://www.frontiersin.org/articles/10.3389/fnins.2022.1040182/fullcerebral ischemia-reperfusionSIRT1neuroprotectionautophagyautophagy signaling pathway
spellingShingle Yingying Tang
Jiaqian Xie
Xiaoping Chen
Lihong Sun
Lili Xu
Xinzhong Chen
A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusion
Frontiers in Neuroscience
cerebral ischemia-reperfusion
SIRT1
neuroprotection
autophagy
autophagy signaling pathway
title A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusion
title_full A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusion
title_fullStr A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusion
title_full_unstemmed A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusion
title_short A novel link between silent information regulator 1 and autophagy in cerebral ischemia-reperfusion
title_sort novel link between silent information regulator 1 and autophagy in cerebral ischemia reperfusion
topic cerebral ischemia-reperfusion
SIRT1
neuroprotection
autophagy
autophagy signaling pathway
url https://www.frontiersin.org/articles/10.3389/fnins.2022.1040182/full
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