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Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism
BACKGROUND: Two active compounds, baicalein and its glycoside baicalin were found in the dried root of Scutellaria baicalensis Georgi, and reported to be neuroprotective in vitro and in vivo. This study aims to evaluate the protective effects of baicalein on the rotenone-induced apoptosis in dopamin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275529/ https://www.ncbi.nlm.nih.gov/pubmed/22264378 http://dx.doi.org/10.1186/1749-8546-7-1 |
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author | Song, Ju-Xian Choi, Mandy Yuen-Man Wong, Kavin Chun-Kit Chung, Winkie Wing-Yan Sze, Stephen Cho-Wing Ng, Tzi-Bun Zhang, Kalin Yan-Bo |
author_facet | Song, Ju-Xian Choi, Mandy Yuen-Man Wong, Kavin Chun-Kit Chung, Winkie Wing-Yan Sze, Stephen Cho-Wing Ng, Tzi-Bun Zhang, Kalin Yan-Bo |
author_sort | Song, Ju-Xian |
collection | PubMed |
description | BACKGROUND: Two active compounds, baicalein and its glycoside baicalin were found in the dried root of Scutellaria baicalensis Georgi, and reported to be neuroprotective in vitro and in vivo. This study aims to evaluate the protective effects of baicalein on the rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to parkinsonism. METHODS: Cell viability and cytotoxicity were determined by MTT assay. The degree of nuclear apoptosis was evaluated with a fluorescent DNA-binding probe Hoechst 33258. The production of reactive oxidative species (ROS) and loss of mitochondrial membrane potential (ΔΨm) were determined by fluorescent staining with DCFH-DA and Rhodanmine 123, respectively. The expression of Bax, Bcl-2, cleaved caspase-3 and phosphorylated ERK1/2 was determined by the Western blots. RESULTS: Baicalein significantly increased viability and decreased rotenone-induced death of SH-SY5Y cells in a dose-dependent manner. Pre- and subsequent co-treatment with baicalein preserved the cell morphology and attenuated the nuclear apoptotic characteristics triggered by rotenone. Baicalein antagonized rotenone-induced overproduction of ROS, loss of ΔΨm, the increased expression of Bax, cleaved caspase-3 and phosphorylated ERK1/2 and the decreased expression of Bcl-2. CONCLUSION: The antioxidative effect, mitochondrial protection and modulation of anti-and pro-apoptotic proteins are related to the neuroprotective effects of baicalein against rotenone induced cell death in SH-SY5Y cells. |
format | Online Article Text |
id | pubmed-3275529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32755292012-02-13 Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism Song, Ju-Xian Choi, Mandy Yuen-Man Wong, Kavin Chun-Kit Chung, Winkie Wing-Yan Sze, Stephen Cho-Wing Ng, Tzi-Bun Zhang, Kalin Yan-Bo Chin Med Research BACKGROUND: Two active compounds, baicalein and its glycoside baicalin were found in the dried root of Scutellaria baicalensis Georgi, and reported to be neuroprotective in vitro and in vivo. This study aims to evaluate the protective effects of baicalein on the rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to parkinsonism. METHODS: Cell viability and cytotoxicity were determined by MTT assay. The degree of nuclear apoptosis was evaluated with a fluorescent DNA-binding probe Hoechst 33258. The production of reactive oxidative species (ROS) and loss of mitochondrial membrane potential (ΔΨm) were determined by fluorescent staining with DCFH-DA and Rhodanmine 123, respectively. The expression of Bax, Bcl-2, cleaved caspase-3 and phosphorylated ERK1/2 was determined by the Western blots. RESULTS: Baicalein significantly increased viability and decreased rotenone-induced death of SH-SY5Y cells in a dose-dependent manner. Pre- and subsequent co-treatment with baicalein preserved the cell morphology and attenuated the nuclear apoptotic characteristics triggered by rotenone. Baicalein antagonized rotenone-induced overproduction of ROS, loss of ΔΨm, the increased expression of Bax, cleaved caspase-3 and phosphorylated ERK1/2 and the decreased expression of Bcl-2. CONCLUSION: The antioxidative effect, mitochondrial protection and modulation of anti-and pro-apoptotic proteins are related to the neuroprotective effects of baicalein against rotenone induced cell death in SH-SY5Y cells. BioMed Central 2012-01-21 /pmc/articles/PMC3275529/ /pubmed/22264378 http://dx.doi.org/10.1186/1749-8546-7-1 Text en Copyright ©2012 Song et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Song, Ju-Xian Choi, Mandy Yuen-Man Wong, Kavin Chun-Kit Chung, Winkie Wing-Yan Sze, Stephen Cho-Wing Ng, Tzi-Bun Zhang, Kalin Yan-Bo Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism |
title | Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism |
title_full | Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism |
title_fullStr | Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism |
title_full_unstemmed | Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism |
title_short | Baicalein antagonizes rotenone-induced apoptosis in dopaminergic SH-SY5Y cells related to Parkinsonism |
title_sort | baicalein antagonizes rotenone-induced apoptosis in dopaminergic sh-sy5y cells related to parkinsonism |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275529/ https://www.ncbi.nlm.nih.gov/pubmed/22264378 http://dx.doi.org/10.1186/1749-8546-7-1 |
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