2. Academic Validation
  3. SIRT1 restores mitochondrial structure and function in rats by activating SIRT3 after cerebral ischemia/reperfusion injury

SIRT1 restores mitochondrial structure and function in rats by activating SIRT3 after cerebral ischemia/reperfusion injury

  • Cell Biol Toxicol. 2024 May 20;40(1):31. doi: 10.1007/s10565-024-09869-2.
Manli Chen # 1 2 3 4,  Ji Liu # 1 2 3 4,  Wenwen Wu # 1 2 3 4,  Ting Guo 1 2 3 4,  Jinjin Yuan 1 2 3 4,  Zhiyun Wu 1 2 3 4,  Zhijian Zheng 1 2 3 4,  Zijun Zhao 1 2 3 4,  Qiang Lin 1 2 3 4,  Nan Liu 5 6 7 8,  Hongbin Chen 9 10 11 12
Affiliations

Affiliations

  • 1 Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
  • 2 Department of Rehabilitation, Fujian Medical University Union Hospital, Fuzhou, China.
  • 3 Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China.
  • 4 Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China.
  • 5 Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China. 9198415014@fjmu.edu.cn.
  • 6 Department of Rehabilitation, Fujian Medical University Union Hospital, Fuzhou, China. 9198415014@fjmu.edu.cn.
  • 7 Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China. 9198415014@fjmu.edu.cn.
  • 8 Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China. 9198415014@fjmu.edu.cn.
  • 9 Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China. hbchen0127@fjmu.edu.cn.
  • 10 Department of Rehabilitation, Fujian Medical University Union Hospital, Fuzhou, China. hbchen0127@fjmu.edu.cn.
  • 11 Fujian Key Laboratory of Molecular Neurology, Fujian Medical University, Fuzhou, China. hbchen0127@fjmu.edu.cn.
  • 12 Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China. hbchen0127@fjmu.edu.cn.
  • # Contributed equally.
PMID: 38767771 DOI: 10.1007/s10565-024-09869-2
Abstract

Mitochondrial dysfunction contributes to cerebral ischemia-reperfusion (CI/R) injury, which can be ameliorated by Sirtuin-3 (SIRT3). Under stress conditions, the SIRT3-promoted mitochondrial functional recovery depends on both its activity and expression. However, the approach to enhance SIRT3 activity after CI/R injury remains unelucidated. In this study, Sprague-Dawley (SD) rats were intracranially injected with either adeno-associated viral Sirtuin-1 (AAV-SIRT1) or AAV-sh_SIRT1 before undergoing transient middle cerebral artery occlusion (tMCAO). Primary cortical neurons were cultured and transfected with lentiviral SIRT1 (LV-SIRT1) and LV-sh_SIRT1 respectively before oxygen-glucose deprivation/reoxygenation (OGD/R). Afterwards, rats and neurons were respectively treated with a selective SIRT3 Inhibitor, 3-(1H-1,2,3-triazol-4-yl) pyridine (3-TYP). The expression, function, and related mechanism of SIRT1 were investigated by Western Blot, flow cytometry, immunofluorescence staining, etc. After CI/R injury, SIRT1 expression decreased in vivo and in vitro. The simulation and immune-analyses reported strong interaction between SIRT1 and SIRT3 in the cerebral mitochondria before and after CI/R. SIRT1 overexpression enhanced SIRT3 activity by increasing the deacetylation of SIRT3, which ameliorated CI/R-induced cerebral infarction, neuronal Apoptosis, oxidative stress, neurological and motor dysfunction, and mitochondrial respiratory chain dysfunction, promoted mitochondrial biogenesis, and retained mitochondrial integrity and mitochondrial morphology. Meanwhile, SIRT1 overexpression alleviated OGD/R-induced neuronal death and mitochondrial bioenergetic deficits. These effects were reversed by AAV-sh_SIRT1 and the neuroprotective effects of SIRT1 were partially offset by 3-TYP. These results suggest that SIRT1 restores the structure and function of mitochondria by activating SIRT3, offering neuroprotection against CI/R injury, which signifies a potential approach for the clinical management of cerebral ischemia.

Keywords

Cerebral ischemia/reperfusion; Mitochondrial structure and function; Neuronal apoptosis; Oxidative stress; SIRT1; SIRT3.

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