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Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction

Antimycin A (AMA) damages mitochondria by inhibiting mitochondrial electron transport and can produce reactive oxygen species (ROS). ROS formation, aging, and reduction of mitochondrial biogenesis contribute to mitochondrial dysfunction. The present study sought to investigate extracts of Scutellari...

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Autores principales: Im, A-Rang, Kim, Young-Hwa, Uddin, Md. Romij, Lee, Hye Won, Chae, Seong Wook, Kim, Yun Hee, Jung, Woo Suk, Kang, Bong Ju, Mun, Chun Sun, Lee, Mi-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437297/
https://www.ncbi.nlm.nih.gov/pubmed/22969827
http://dx.doi.org/10.1155/2012/517965
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author Im, A-Rang
Kim, Young-Hwa
Uddin, Md. Romij
Lee, Hye Won
Chae, Seong Wook
Kim, Yun Hee
Jung, Woo Suk
Kang, Bong Ju
Mun, Chun Sun
Lee, Mi-Young
author_facet Im, A-Rang
Kim, Young-Hwa
Uddin, Md. Romij
Lee, Hye Won
Chae, Seong Wook
Kim, Yun Hee
Jung, Woo Suk
Kang, Bong Ju
Mun, Chun Sun
Lee, Mi-Young
author_sort Im, A-Rang
collection PubMed
description Antimycin A (AMA) damages mitochondria by inhibiting mitochondrial electron transport and can produce reactive oxygen species (ROS). ROS formation, aging, and reduction of mitochondrial biogenesis contribute to mitochondrial dysfunction. The present study sought to investigate extracts of Scutellaria baicalensis and its flavonoids (baicalin, baicalein, and wogonin), whether they could protect mitochondria against oxidative damage. The viability of L6 cells treated with AMA increased in the presence of flavonoids and extracts of S. baicalensis. ATP production decreased in the AMA treated group, but increased by 50% in cells treated with flavonoids (except wogonin) and extracts of S. baicalensis compared to AMA-treated group. AMA treatment caused a significant reduction (depolarized) in mitochondrial membrane potential (MMP), whereas flavonoid treatment induced a significant increase in MMP. Mitochondrial superoxide levels increased in AMA treated cells, whereas its levels decreased when cells were treated with flavonoids or extracts of S. baicalensis. L6 cells treated with flavonoids and extracts of S. baicalensis increased their levels of protein expression compared with AMA-treated cells, especially water extracts performed the highest levels of protein expression. These results suggest that the S. baicalensis extracts and flavonoids protect against AMA-induced mitochondrial dysfunction by increasing ATP production, upregulating MMP, and enhancing mitochondrial function.
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spelling pubmed-34372972012-09-11 Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction Im, A-Rang Kim, Young-Hwa Uddin, Md. Romij Lee, Hye Won Chae, Seong Wook Kim, Yun Hee Jung, Woo Suk Kang, Bong Ju Mun, Chun Sun Lee, Mi-Young Evid Based Complement Alternat Med Research Article Antimycin A (AMA) damages mitochondria by inhibiting mitochondrial electron transport and can produce reactive oxygen species (ROS). ROS formation, aging, and reduction of mitochondrial biogenesis contribute to mitochondrial dysfunction. The present study sought to investigate extracts of Scutellaria baicalensis and its flavonoids (baicalin, baicalein, and wogonin), whether they could protect mitochondria against oxidative damage. The viability of L6 cells treated with AMA increased in the presence of flavonoids and extracts of S. baicalensis. ATP production decreased in the AMA treated group, but increased by 50% in cells treated with flavonoids (except wogonin) and extracts of S. baicalensis compared to AMA-treated group. AMA treatment caused a significant reduction (depolarized) in mitochondrial membrane potential (MMP), whereas flavonoid treatment induced a significant increase in MMP. Mitochondrial superoxide levels increased in AMA treated cells, whereas its levels decreased when cells were treated with flavonoids or extracts of S. baicalensis. L6 cells treated with flavonoids and extracts of S. baicalensis increased their levels of protein expression compared with AMA-treated cells, especially water extracts performed the highest levels of protein expression. These results suggest that the S. baicalensis extracts and flavonoids protect against AMA-induced mitochondrial dysfunction by increasing ATP production, upregulating MMP, and enhancing mitochondrial function. Hindawi Publishing Corporation 2012 2012-08-30 /pmc/articles/PMC3437297/ /pubmed/22969827 http://dx.doi.org/10.1155/2012/517965 Text en Copyright © 2012 A-Rang Im et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Im, A-Rang
Kim, Young-Hwa
Uddin, Md. Romij
Lee, Hye Won
Chae, Seong Wook
Kim, Yun Hee
Jung, Woo Suk
Kang, Bong Ju
Mun, Chun Sun
Lee, Mi-Young
Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction
title Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction
title_full Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction
title_fullStr Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction
title_full_unstemmed Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction
title_short Scutellaria baicalensis Extracts and Flavonoids Protect Rat L6 Cells from Antimycin A-Induced Mitochondrial Dysfunction
title_sort scutellaria baicalensis extracts and flavonoids protect rat l6 cells from antimycin a-induced mitochondrial dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437297/
https://www.ncbi.nlm.nih.gov/pubmed/22969827
http://dx.doi.org/10.1155/2012/517965
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