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Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum
In this study we first focused on the effects of a novel proteoglycan extracted from Ganoderma lucidum (FYGL) on mitochondrial biogenesis, because mitochondrial dysfunction is highly related to insulin resistance. We found that FYGL can decrease ROS levels and increase ATP content in rat skeletal mu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059857/ https://www.ncbi.nlm.nih.gov/pubmed/35520529 http://dx.doi.org/10.1039/c8ra09482a |
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author | Yang, Zhou Zhang, Zeng Zhao, Juan He, Yanming Yang, Hongjie Zhou, Ping |
author_facet | Yang, Zhou Zhang, Zeng Zhao, Juan He, Yanming Yang, Hongjie Zhou, Ping |
author_sort | Yang, Zhou |
collection | PubMed |
description | In this study we first focused on the effects of a novel proteoglycan extracted from Ganoderma lucidum (FYGL) on mitochondrial biogenesis, because mitochondrial dysfunction is highly related to insulin resistance. We found that FYGL can decrease ROS levels and increase ATP content in rat skeletal muscle L6 cells. In PGC-1α silent cells, FYGL increased expression of PGC-1α and positively modulated the Sirt1/PGC-1α pathway. Moreover, FYGL orally administered up-regulated the mitochondrial DNA (mtDNA) copy number and the related gene expressions that control mitochondrial biogenesis in ob/ob mice. Our work well elucidated the mechanism of FYGL ameliorating insulin resistance in the aspect of energy metabolism. |
format | Online Article Text |
id | pubmed-9059857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90598572022-05-04 Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum Yang, Zhou Zhang, Zeng Zhao, Juan He, Yanming Yang, Hongjie Zhou, Ping RSC Adv Chemistry In this study we first focused on the effects of a novel proteoglycan extracted from Ganoderma lucidum (FYGL) on mitochondrial biogenesis, because mitochondrial dysfunction is highly related to insulin resistance. We found that FYGL can decrease ROS levels and increase ATP content in rat skeletal muscle L6 cells. In PGC-1α silent cells, FYGL increased expression of PGC-1α and positively modulated the Sirt1/PGC-1α pathway. Moreover, FYGL orally administered up-regulated the mitochondrial DNA (mtDNA) copy number and the related gene expressions that control mitochondrial biogenesis in ob/ob mice. Our work well elucidated the mechanism of FYGL ameliorating insulin resistance in the aspect of energy metabolism. The Royal Society of Chemistry 2019-01-18 /pmc/articles/PMC9059857/ /pubmed/35520529 http://dx.doi.org/10.1039/c8ra09482a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yang, Zhou Zhang, Zeng Zhao, Juan He, Yanming Yang, Hongjie Zhou, Ping Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum |
title | Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum |
title_full | Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum |
title_fullStr | Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum |
title_full_unstemmed | Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum |
title_short | Modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from Ganoderma lucidum |
title_sort | modulation of energy metabolism and mitochondrial biogenesis by a novel proteoglycan from ganoderma lucidum |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059857/ https://www.ncbi.nlm.nih.gov/pubmed/35520529 http://dx.doi.org/10.1039/c8ra09482a |
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