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Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1

Introduction: Ginkgolide B (GB), which is an active constituent derived from Ginkgo biloba leaves, has been reported to ameliorate Alzheimer’s disease (AD), ischemic stroke, as well as other neurodegenerative diseases due to its viable immunosuppressive and anti-inflammatory functions. However, it h...

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Autores principales: Cao, Yile, Yang, Lei, Cheng, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273931/
https://www.ncbi.nlm.nih.gov/pubmed/35837278
http://dx.doi.org/10.3389/fphar.2022.941094
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author Cao, Yile
Yang, Lei
Cheng, Hong
author_facet Cao, Yile
Yang, Lei
Cheng, Hong
author_sort Cao, Yile
collection PubMed
description Introduction: Ginkgolide B (GB), which is an active constituent derived from Ginkgo biloba leaves, has been reported to ameliorate Alzheimer’s disease (AD), ischemic stroke, as well as other neurodegenerative diseases due to its viable immunosuppressive and anti-inflammatory functions. However, it has yet to be proven whether GB inhibits neuronal apoptosis in ischemic stroke. Methods: In the present research, the inhibition function of GB on neuronal apoptosis and its underpinning process(s) after cerebral ischemia were studied through transient middle cerebral artery occlusion (t-MCAO) in an in vivo rat model as well as in cultured SH-SY5Y cells subjected to oxygen and glucose deprivation (OGD)/reoxygenation in vitro. The neurological score was calculated and Nissl and TUNEL staining were performed to evaluate the stroke outcome, neuronal loss, and neuronal apoptosis. Subsequently, the western blot was utilized to detect Bcl2 and p-AMPK/AMPK expression. Results: Compared to t-MCAO rats, rats receiving GB treatment showed a significant reduction of neuronal loss and apoptosis and improved neurological behavior at 72 h after MCAO. GB treatment also upregulated the expression of Bcl2 and p-AMPK. In vitro, GB suppressed the apoptosis in OGD/reoxygenation-challenged neuronal SH-SY5Y cells through AMPK activation. Conclusions: Our observations suggest that GB enhanced AMPK activation in neural cells, reducing neuronal apoptosis, thus eventually preventing ischemic stroke.
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spelling pubmed-92739312022-07-13 Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1 Cao, Yile Yang, Lei Cheng, Hong Front Pharmacol Pharmacology Introduction: Ginkgolide B (GB), which is an active constituent derived from Ginkgo biloba leaves, has been reported to ameliorate Alzheimer’s disease (AD), ischemic stroke, as well as other neurodegenerative diseases due to its viable immunosuppressive and anti-inflammatory functions. However, it has yet to be proven whether GB inhibits neuronal apoptosis in ischemic stroke. Methods: In the present research, the inhibition function of GB on neuronal apoptosis and its underpinning process(s) after cerebral ischemia were studied through transient middle cerebral artery occlusion (t-MCAO) in an in vivo rat model as well as in cultured SH-SY5Y cells subjected to oxygen and glucose deprivation (OGD)/reoxygenation in vitro. The neurological score was calculated and Nissl and TUNEL staining were performed to evaluate the stroke outcome, neuronal loss, and neuronal apoptosis. Subsequently, the western blot was utilized to detect Bcl2 and p-AMPK/AMPK expression. Results: Compared to t-MCAO rats, rats receiving GB treatment showed a significant reduction of neuronal loss and apoptosis and improved neurological behavior at 72 h after MCAO. GB treatment also upregulated the expression of Bcl2 and p-AMPK. In vitro, GB suppressed the apoptosis in OGD/reoxygenation-challenged neuronal SH-SY5Y cells through AMPK activation. Conclusions: Our observations suggest that GB enhanced AMPK activation in neural cells, reducing neuronal apoptosis, thus eventually preventing ischemic stroke. Frontiers Media S.A. 2022-06-28 /pmc/articles/PMC9273931/ /pubmed/35837278 http://dx.doi.org/10.3389/fphar.2022.941094 Text en Copyright © 2022 Cao, Yang and Cheng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Cao, Yile
Yang, Lei
Cheng, Hong
Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1
title Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1
title_full Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1
title_fullStr Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1
title_full_unstemmed Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1
title_short Ginkgolide B Protects Against Ischemic Stroke via Targeting AMPK/PINK1
title_sort ginkgolide b protects against ischemic stroke via targeting ampk/pink1
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273931/
https://www.ncbi.nlm.nih.gov/pubmed/35837278
http://dx.doi.org/10.3389/fphar.2022.941094
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