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Herbal formula PM012 induces neuroprotection in stroke brain
Stroke is a major cause of long-term disability world-wide. Limited pharmacological therapy has been used in stroke patients. Previous studies indicated that herb formula PM012 is neuroprotective against neurotoxin trimethyltin in rat brain, and improved learning and memory in animal models of Alzhe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946208/ https://www.ncbi.nlm.nih.gov/pubmed/36812289 http://dx.doi.org/10.1371/journal.pone.0281421 |
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author | Wu, Kuo-Jen Wang, Yu-Syuan Hung, Tsai-Wei Bae, Eun-Kyung Chen, Yun-Hsiang Kim, Chan-Kyu Yoo, Dai-Won Kim, Gyeong-Soon Yu, Seong-Jin |
author_facet | Wu, Kuo-Jen Wang, Yu-Syuan Hung, Tsai-Wei Bae, Eun-Kyung Chen, Yun-Hsiang Kim, Chan-Kyu Yoo, Dai-Won Kim, Gyeong-Soon Yu, Seong-Jin |
author_sort | Wu, Kuo-Jen |
collection | PubMed |
description | Stroke is a major cause of long-term disability world-wide. Limited pharmacological therapy has been used in stroke patients. Previous studies indicated that herb formula PM012 is neuroprotective against neurotoxin trimethyltin in rat brain, and improved learning and memory in animal models of Alzheimer’s disease. Its action in stroke has not been reported. This study aims to determine PM012-mediated neural protection in cellular and animal models of stroke. Glutamate-mediated neuronal loss and apoptosis were examined in rat primary cortical neuronal cultures. Cultured cells were overexpressed with a Ca++ probe (gCaMP5) by AAV1 and were used to examine Ca++ influx (Ca++i). Adult rats received PM012 before transient middle cerebral artery occlusion (MCAo). Brain tissues were collected for infarction and qRTPCR analysis. In rat primary cortical neuronal cultures, PM012 significantly antagonized glutamate-mediated TUNEL and neuronal loss, as well as NMDA-mediated Ca++i. PM012 significantly reduced brain infarction and improved locomotor activity in stroke rats. PM012 attenuated the expression of IBA1, IL6, and CD86, while upregulated CD206 in the infarcted cortex. ATF6, Bip, CHOP, IRE1, and PERK were significantly down-regulated by PM012. Using HPLC, two potential bioactive molecules, paeoniflorin and 5-hydroxymethylfurfural, were identified in the PM012 extract. Taken together, our data suggest that PM012 is neuroprotective against stroke. The mechanisms of action involve inhibition of Ca++i, inflammation, and apoptosis. |
format | Online Article Text |
id | pubmed-9946208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99462082023-02-23 Herbal formula PM012 induces neuroprotection in stroke brain Wu, Kuo-Jen Wang, Yu-Syuan Hung, Tsai-Wei Bae, Eun-Kyung Chen, Yun-Hsiang Kim, Chan-Kyu Yoo, Dai-Won Kim, Gyeong-Soon Yu, Seong-Jin PLoS One Research Article Stroke is a major cause of long-term disability world-wide. Limited pharmacological therapy has been used in stroke patients. Previous studies indicated that herb formula PM012 is neuroprotective against neurotoxin trimethyltin in rat brain, and improved learning and memory in animal models of Alzheimer’s disease. Its action in stroke has not been reported. This study aims to determine PM012-mediated neural protection in cellular and animal models of stroke. Glutamate-mediated neuronal loss and apoptosis were examined in rat primary cortical neuronal cultures. Cultured cells were overexpressed with a Ca++ probe (gCaMP5) by AAV1 and were used to examine Ca++ influx (Ca++i). Adult rats received PM012 before transient middle cerebral artery occlusion (MCAo). Brain tissues were collected for infarction and qRTPCR analysis. In rat primary cortical neuronal cultures, PM012 significantly antagonized glutamate-mediated TUNEL and neuronal loss, as well as NMDA-mediated Ca++i. PM012 significantly reduced brain infarction and improved locomotor activity in stroke rats. PM012 attenuated the expression of IBA1, IL6, and CD86, while upregulated CD206 in the infarcted cortex. ATF6, Bip, CHOP, IRE1, and PERK were significantly down-regulated by PM012. Using HPLC, two potential bioactive molecules, paeoniflorin and 5-hydroxymethylfurfural, were identified in the PM012 extract. Taken together, our data suggest that PM012 is neuroprotective against stroke. The mechanisms of action involve inhibition of Ca++i, inflammation, and apoptosis. Public Library of Science 2023-02-22 /pmc/articles/PMC9946208/ /pubmed/36812289 http://dx.doi.org/10.1371/journal.pone.0281421 Text en © 2023 Wu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wu, Kuo-Jen Wang, Yu-Syuan Hung, Tsai-Wei Bae, Eun-Kyung Chen, Yun-Hsiang Kim, Chan-Kyu Yoo, Dai-Won Kim, Gyeong-Soon Yu, Seong-Jin Herbal formula PM012 induces neuroprotection in stroke brain |
title | Herbal formula PM012 induces neuroprotection in stroke brain |
title_full | Herbal formula PM012 induces neuroprotection in stroke brain |
title_fullStr | Herbal formula PM012 induces neuroprotection in stroke brain |
title_full_unstemmed | Herbal formula PM012 induces neuroprotection in stroke brain |
title_short | Herbal formula PM012 induces neuroprotection in stroke brain |
title_sort | herbal formula pm012 induces neuroprotection in stroke brain |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9946208/ https://www.ncbi.nlm.nih.gov/pubmed/36812289 http://dx.doi.org/10.1371/journal.pone.0281421 |
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