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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9273931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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