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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
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.
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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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