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Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke

Tanhuo formula (THF), a traditional Chinese medicinal formula, has been demonstrated to be effective in the clinical treatment of acute ischemic stroke (AIS). However, its active ingredients, potential targets, and molecular mechanisms remain unknown. Based on the validation of active ingredient con...

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Autores principales: Nie, Yuting, Wen, Lulu, Li, Hui, Song, Juexian, Wang, Ningqun, Huang, Liyuan, Gao, Li, Qu, Miao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087855/
https://www.ncbi.nlm.nih.gov/pubmed/35559267
http://dx.doi.org/10.3389/fphar.2022.859244
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author Nie, Yuting
Wen, Lulu
Li, Hui
Song, Juexian
Wang, Ningqun
Huang, Liyuan
Gao, Li
Qu, Miao
author_facet Nie, Yuting
Wen, Lulu
Li, Hui
Song, Juexian
Wang, Ningqun
Huang, Liyuan
Gao, Li
Qu, Miao
author_sort Nie, Yuting
collection PubMed
description Tanhuo formula (THF), a traditional Chinese medicinal formula, has been demonstrated to be effective in the clinical treatment of acute ischemic stroke (AIS). However, its active ingredients, potential targets, and molecular mechanisms remain unknown. Based on the validation of active ingredient concentrations, our study attempted to elucidate the possible mechanisms of THF based on network pharmacological analysis and experimental validation. Components of THF were screened using network pharmacological analysis, and a compound–target network and protein–protein interaction (PPI) network were constructed. In total, 42 bioactive compounds and 159 THF targets related to AIS were identified. The PPI network identified AKT1, TNF, IL6, IL1B, and CASP3 as key targets. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis demonstrated that the inflammation and apoptotic pathways were enriched by multiple targets. The main components of THF were identified via high-performance liquid chromatography. Subsequently, a validation experiment was conducted, and the expressions of GFAP, C3, TNF-α, and IL-6 were detected via immunofluorescence staining, confirming the inflammatory response at 30 min and 3 days post injury. Immunohistochemical staining for caspase-3 and TUNEL was also performed to assess apoptosis at the same time points. These results indicate that THF can effectively decrease neural cell apoptosis through the caspase-3 pathway and restrain excessive abnormal activation of astrocytes and the release of TNF-α and IL-6, which might be accompanied by the recovery of motor function. Thus, THF may serve as a promising therapeutic strategy for AIS through multiple targets, components, and pathways.
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spelling pubmed-90878552022-05-11 Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke Nie, Yuting Wen, Lulu Li, Hui Song, Juexian Wang, Ningqun Huang, Liyuan Gao, Li Qu, Miao Front Pharmacol Pharmacology Tanhuo formula (THF), a traditional Chinese medicinal formula, has been demonstrated to be effective in the clinical treatment of acute ischemic stroke (AIS). However, its active ingredients, potential targets, and molecular mechanisms remain unknown. Based on the validation of active ingredient concentrations, our study attempted to elucidate the possible mechanisms of THF based on network pharmacological analysis and experimental validation. Components of THF were screened using network pharmacological analysis, and a compound–target network and protein–protein interaction (PPI) network were constructed. In total, 42 bioactive compounds and 159 THF targets related to AIS were identified. The PPI network identified AKT1, TNF, IL6, IL1B, and CASP3 as key targets. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis demonstrated that the inflammation and apoptotic pathways were enriched by multiple targets. The main components of THF were identified via high-performance liquid chromatography. Subsequently, a validation experiment was conducted, and the expressions of GFAP, C3, TNF-α, and IL-6 were detected via immunofluorescence staining, confirming the inflammatory response at 30 min and 3 days post injury. Immunohistochemical staining for caspase-3 and TUNEL was also performed to assess apoptosis at the same time points. These results indicate that THF can effectively decrease neural cell apoptosis through the caspase-3 pathway and restrain excessive abnormal activation of astrocytes and the release of TNF-α and IL-6, which might be accompanied by the recovery of motor function. Thus, THF may serve as a promising therapeutic strategy for AIS through multiple targets, components, and pathways. Frontiers Media S.A. 2022-04-26 /pmc/articles/PMC9087855/ /pubmed/35559267 http://dx.doi.org/10.3389/fphar.2022.859244 Text en Copyright © 2022 Nie, Wen, Li, Song, Wang, Huang, Gao and Qu. 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
Nie, Yuting
Wen, Lulu
Li, Hui
Song, Juexian
Wang, Ningqun
Huang, Liyuan
Gao, Li
Qu, Miao
Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke
title Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke
title_full Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke
title_fullStr Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke
title_full_unstemmed Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke
title_short Tanhuo Formula Inhibits Astrocyte Activation and Apoptosis in Acute Ischemic Stroke
title_sort tanhuo formula inhibits astrocyte activation and apoptosis in acute ischemic stroke
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087855/
https://www.ncbi.nlm.nih.gov/pubmed/35559267
http://dx.doi.org/10.3389/fphar.2022.859244
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