Propofol improves neuronal apoptosis and oxidative damage mediated by cerebral ischemia-reperfusion by regulating the miR-6838-5p/AQP11 axis

Introduction This study aimed to elucidate the mechanism by which Propofol (PPF) exerts its effects in cerebral ischemia-reperfusion injury (CI/RI). Material and methods A rat model of CI/RI was established via middle cerebral artery occlusion/reperfusion (MCAO/R). MCAO/R rats were pre-treated with PPF (10 mg/kg) via intraperitoneal injection. Additionally, 48 hours before PPF administration, miR-6838-5p agomir/antagomir and aquaporin-11 (AQP11) lentiviral overexpression vectors were injected into MCAO/R rats. Infarct size was determined using 2,3,5-triphenyl tetrazolium chloride staining. Neurological function was assessed using standardized scoring, and cerebral edema was measured by determining brain water content. Hematoxylin-eosin staining, Nissl staining, and Terminal deoxynucleotidyl transferase dUTP nick end labeling staining were performed on brain tissues. Inflammatory and oxidative markers were evaluated. A hypoxia/reoxygenation (H/R) injury model was established in PC12 cells to assess miR-6838-5p and AQP11 expression levels, as well as cell viability and apoptosis. Results The lethal dose 50 (LD₅₀) of PPF in rats was determined to be 22.6 mg/kg, significantly higher than the therapeutic dose. PPF or overexpression of miR-6838-5p resulted in reduced cerebral infarct size, neuronal necrosis, and apoptosis, increased Nissl bodies, and decreased brain edema, apoptosis, tumor necrosis factor-α, interleukin-1β, and malondialdehyde (MDA) levels. Glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) activities were elevated in MCAO/R rats treated with PPF. These protective effects of PPF were reversed by miR-6838-5p knockdown or AQP11 overexpression. PPF ameliorated H/R-induced neuronal damage, enhanced neuronal activity, reduced apoptosis and MDA production, and increased GSH-Px and SOD levels. Conclusions PPF ameliorates CI/RI by modulating the miR-6838-5p/AQP11 axis.

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Journal
Archives of Medical Science
Published
2025-04-20
DOI
https://doi.org/10.5114/aoms/201185
Primary Topic
Anesthesia and Neurotoxicity Research
Type
article
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article

Propofol improves neuronal apoptosis and oxidative damage mediated by cerebral ischemia-reperfusion by regulating the miR-6838-5p/AQP11 axis

Xiu-Qin Wang, Yue‐Ying Zhang, Liang Zhao, Yangyang Shen
Archives of Medical Science
Anesthesia and Neurotoxicity Research
article

Propofol improves neuronal apoptosis and oxidative damage mediated by cerebral ischemia-reperfusion by regulating the miR-6838-5p/AQP11 axis

Xiu-Qin Wang, Yue‐Ying Zhang, Liang Zhao, Yangyang Shen
article en

Abstract

Introduction This study aimed to elucidate the mechanism by which Propofol (PPF) exerts its effects in cerebral ischemia-reperfusion injury (CI/RI). Material and methods A rat model of CI/RI was established via middle cerebral artery occlusion/reperfusion (MCAO/R). MCAO/R rats were pre-treated with PPF (10 mg/kg) via intraperitoneal injection. Additionally, 48 hours before PPF administration, miR-6838-5p agomir/antagomir and aquaporin-11 (AQP11) lentiviral overexpression vectors were injected into MCAO/R rats. Infarct size was determined using 2,3,5-triphenyl tetrazolium chloride staining. Neurological function was assessed using standardized scoring, and cerebral edema was measured by determining brain water content. Hematoxylin-eosin staining, Nissl staining, and Terminal deoxynucleotidyl transferase dUTP nick end labeling staining were performed on brain tissues. Inflammatory and oxidative markers were evaluated. A hypoxia/reoxygenation (H/R) injury model was established in PC12 cells to assess miR-6838-5p and AQP11 expression levels, as well as cell viability and apoptosis. Results The lethal dose 50 (LD₅₀) of PPF in rats was determined to be 22.6 mg/kg, significantly higher than the therapeutic dose. PPF or overexpression of miR-6838-5p resulted in reduced cerebral infarct size, neuronal necrosis, and apoptosis, increased Nissl bodies, and decreased brain edema, apoptosis, tumor necrosis factor-α, interleukin-1β, and malondialdehyde (MDA) levels. Glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) activities were elevated in MCAO/R rats treated with PPF. These protective effects of PPF were reversed by miR-6838-5p knockdown or AQP11 overexpression. PPF ameliorated H/R-induced neuronal damage, enhanced neuronal activity, reduced apoptosis and MDA production, and increased GSH-Px and SOD levels. Conclusions PPF ameliorates CI/RI by modulating the miR-6838-5p/AQP11 axis.

Archives of Medical Science
Shandong Tumor Hospital (CN), 82th Hospital of Pla (CN), Shandong First Medical University (CN)
Openalex Percentile: Top 90%
Anesthesia and Neurotoxicity Research
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