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Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats
Stroke is one of the leading causes of death from diseases. When the blood supply to the brain tissue is interrupted, neuronal core death occurs due to the lack of glucose and oxygen in min. Blood pressure lowering after ischemic stroke was proven to be an effective strategy to achieve neurovascular...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673071/ https://www.ncbi.nlm.nih.gov/pubmed/36331022 http://dx.doi.org/10.3892/mmr.2022.12890 |
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author | Shen, Fengyan Meng, Yong He, Yuhai Huang, Bowan Huang, Jinxin Wang, Lu |
author_facet | Shen, Fengyan Meng, Yong He, Yuhai Huang, Bowan Huang, Jinxin Wang, Lu |
author_sort | Shen, Fengyan |
collection | PubMed |
description | Stroke is one of the leading causes of death from diseases. When the blood supply to the brain tissue is interrupted, neuronal core death occurs due to the lack of glucose and oxygen in min. Blood pressure lowering after ischemic stroke was proven to be an effective strategy to achieve neurovascular protection and reduce the risk of recurrent stroke. Astragaloside IV is a pure small molecular compound isolated from Radix Astragali, and it is well documented that astragaloside IV has neuroprotective effect on cerebral ischemia reperfusion (CIR) injury through many mechanisms, including antioxidant, anti-inflammatory and anti-apoptotic. The present study adopted mean arterial pressure (MAP) monitoring, neurological scoring, 2,3,5-triphenyltetrazolium chloride staining, enzyme-linked immuno-sorbent assay, western blotting and other experimental methods to investigate the effect of astragaloside IV on systemic blood pressure during CIR in a middle cerebral artery occlusion animal model. It was demonstrated that astragaloside IV pretreatment significantly alleviated CIR injury as previously reported. In addition, the elevation of MAP during CIR was significantly inhibited by astragaloside IV administration. Moreover, it was revealed that the expression of Na(+)-K(+)−2Cl(−) cotransporter isoform 1 in the hypothalamus was inhibited and the subsequent synthesis of vasopressin was reduced by astragaloside IV pretreatment in the CIR animal model. In conclusion, astragaloside IV may alleviate CIR injury partially by lowering systemic blood pressure. |
format | Online Article Text |
id | pubmed-9673071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-96730712022-11-22 Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats Shen, Fengyan Meng, Yong He, Yuhai Huang, Bowan Huang, Jinxin Wang, Lu Mol Med Rep Articles Stroke is one of the leading causes of death from diseases. When the blood supply to the brain tissue is interrupted, neuronal core death occurs due to the lack of glucose and oxygen in min. Blood pressure lowering after ischemic stroke was proven to be an effective strategy to achieve neurovascular protection and reduce the risk of recurrent stroke. Astragaloside IV is a pure small molecular compound isolated from Radix Astragali, and it is well documented that astragaloside IV has neuroprotective effect on cerebral ischemia reperfusion (CIR) injury through many mechanisms, including antioxidant, anti-inflammatory and anti-apoptotic. The present study adopted mean arterial pressure (MAP) monitoring, neurological scoring, 2,3,5-triphenyltetrazolium chloride staining, enzyme-linked immuno-sorbent assay, western blotting and other experimental methods to investigate the effect of astragaloside IV on systemic blood pressure during CIR in a middle cerebral artery occlusion animal model. It was demonstrated that astragaloside IV pretreatment significantly alleviated CIR injury as previously reported. In addition, the elevation of MAP during CIR was significantly inhibited by astragaloside IV administration. Moreover, it was revealed that the expression of Na(+)-K(+)−2Cl(−) cotransporter isoform 1 in the hypothalamus was inhibited and the subsequent synthesis of vasopressin was reduced by astragaloside IV pretreatment in the CIR animal model. In conclusion, astragaloside IV may alleviate CIR injury partially by lowering systemic blood pressure. D.A. Spandidos 2022-11-03 /pmc/articles/PMC9673071/ /pubmed/36331022 http://dx.doi.org/10.3892/mmr.2022.12890 Text en Copyright: © Shen et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Shen, Fengyan Meng, Yong He, Yuhai Huang, Bowan Huang, Jinxin Wang, Lu Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats |
title | Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats |
title_full | Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats |
title_fullStr | Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats |
title_full_unstemmed | Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats |
title_short | Antihypertension effect of astragaloside IV during cerebral ischemia reperfusion in rats |
title_sort | antihypertension effect of astragaloside iv during cerebral ischemia reperfusion in rats |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673071/ https://www.ncbi.nlm.nih.gov/pubmed/36331022 http://dx.doi.org/10.3892/mmr.2022.12890 |
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