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Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia

BACKGROUND: Chronic cerebral hypoperfusion has been well-characterized as a common pathological status contributing to vascular dementia (VD). In this study, the neuroprotective effect of modified Bo-yang-Hwan-O Tang (mBHT), a polyherbal medicine for ischemic stroke, was investigated in a rat model...

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Autores principales: Oh, Tae Woo, Jung, Hyo Won, Park, Yong-Ki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522858/
https://www.ncbi.nlm.nih.gov/pubmed/26246747
http://dx.doi.org/10.4103/0973-1296.160445
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author Oh, Tae Woo
Jung, Hyo Won
Park, Yong-Ki
author_facet Oh, Tae Woo
Jung, Hyo Won
Park, Yong-Ki
author_sort Oh, Tae Woo
collection PubMed
description BACKGROUND: Chronic cerebral hypoperfusion has been well-characterized as a common pathological status contributing to vascular dementia (VD). In this study, the neuroprotective effect of modified Bo-yang-Hwan-O Tang (mBHT), a polyherbal medicine for ischemic stroke, was investigated in a rat model for global ischemia. MATERIALS AND METHODS: Global ischemia model was prepared in Sprague-Dawley rats by the permanent occlusion of bilateral common carotid arteries (two-vessel occlusion [2VO])-induced chronic cerebral hypoperfusion. mBHT at doses of 250 and 500 mg/kg was orally administrated for 4 weeks once a day, 24 h after 2VO. Histopathological change of the hippocampal region was observed by hematoxylin and eosin, Nissl, and Fluoro-Jade B staining and immunohistochemistry with anti-glial fibrillary acidic protein and anti-neuronal nuclei antibodies. The expression of Bax, Bcl-2, and caspase-3 was investigated in the hippocampus by Western blot. The nuclear factor-kappa B (NF-κB) expression was also analyzed in hippocampal CA1 region using immunofluorescence staining. RESULTS: The administration of mBHT at doses of 250 and 500 mg/kg significantly inhibited chronic cerebral hypoperfusion-induced neuronal damage and astroglial activation in the hippocampal CA1 region in 2VO rats. mBHT increased the NF-κB expression in the CA1 neuronal cells but decreased in activated astrocytes. In addition, mBHT significantly decreased the hippocampal expression of Bax and caspase-3 and increased the Bcl-2 expression in 2VO rats. CONCLUSIONS: Our data indicate that mBHT has a neuroprotective property in VD induced by chronic cerebral hypoperfusion through inhibiting the hippocampal neuronal damage and astrogliosis.
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spelling pubmed-45228582015-08-05 Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia Oh, Tae Woo Jung, Hyo Won Park, Yong-Ki Pharmacogn Mag Original Article BACKGROUND: Chronic cerebral hypoperfusion has been well-characterized as a common pathological status contributing to vascular dementia (VD). In this study, the neuroprotective effect of modified Bo-yang-Hwan-O Tang (mBHT), a polyherbal medicine for ischemic stroke, was investigated in a rat model for global ischemia. MATERIALS AND METHODS: Global ischemia model was prepared in Sprague-Dawley rats by the permanent occlusion of bilateral common carotid arteries (two-vessel occlusion [2VO])-induced chronic cerebral hypoperfusion. mBHT at doses of 250 and 500 mg/kg was orally administrated for 4 weeks once a day, 24 h after 2VO. Histopathological change of the hippocampal region was observed by hematoxylin and eosin, Nissl, and Fluoro-Jade B staining and immunohistochemistry with anti-glial fibrillary acidic protein and anti-neuronal nuclei antibodies. The expression of Bax, Bcl-2, and caspase-3 was investigated in the hippocampus by Western blot. The nuclear factor-kappa B (NF-κB) expression was also analyzed in hippocampal CA1 region using immunofluorescence staining. RESULTS: The administration of mBHT at doses of 250 and 500 mg/kg significantly inhibited chronic cerebral hypoperfusion-induced neuronal damage and astroglial activation in the hippocampal CA1 region in 2VO rats. mBHT increased the NF-κB expression in the CA1 neuronal cells but decreased in activated astrocytes. In addition, mBHT significantly decreased the hippocampal expression of Bax and caspase-3 and increased the Bcl-2 expression in 2VO rats. CONCLUSIONS: Our data indicate that mBHT has a neuroprotective property in VD induced by chronic cerebral hypoperfusion through inhibiting the hippocampal neuronal damage and astrogliosis. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4522858/ /pubmed/26246747 http://dx.doi.org/10.4103/0973-1296.160445 Text en Copyright: © Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Oh, Tae Woo
Jung, Hyo Won
Park, Yong-Ki
Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia
title Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia
title_full Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia
title_fullStr Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia
title_full_unstemmed Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia
title_short Effect of modified Bo-yang-Hwan-o-Tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia
title_sort effect of modified bo-yang-hwan-o-tang, a polyherbal medicine on the hippocampal neuronal damage in a rat model of global ischemia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522858/
https://www.ncbi.nlm.nih.gov/pubmed/26246747
http://dx.doi.org/10.4103/0973-1296.160445
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