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Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders
Pachymic acid (Pac), a major bioactive constituent of Poria cocos, is an antioxidant that inhibits triglyceride (TG) accumulation. To the best of our knowledge, the present study investigated for the first time whether Pac activated sirtuin 6 (SIRT6) signaling to alleviate oleic acid (OA)-palmitic a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236048/ https://www.ncbi.nlm.nih.gov/pubmed/37273757 http://dx.doi.org/10.3892/etm.2023.12019 |
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author | Pan, Zhi-Sen Chen, Yan-Ling Tang, Kai-Jia Liu, Zhang-Zhou Liang, Jia-Li Guan, Yan-Hao Xin, Xiao-Yi Liu, Chang-Hui Shen, Chuang-Peng |
author_facet | Pan, Zhi-Sen Chen, Yan-Ling Tang, Kai-Jia Liu, Zhang-Zhou Liang, Jia-Li Guan, Yan-Hao Xin, Xiao-Yi Liu, Chang-Hui Shen, Chuang-Peng |
author_sort | Pan, Zhi-Sen |
collection | PubMed |
description | Pachymic acid (Pac), a major bioactive constituent of Poria cocos, is an antioxidant that inhibits triglyceride (TG) accumulation. To the best of our knowledge, the present study investigated for the first time whether Pac activated sirtuin 6 (SIRT6) signaling to alleviate oleic acid (OA)-palmitic acid (PA)-induced lipid metabolism disorders in mouse primary hepatocytes (MPHs). In the present study, MPHs challenged with Pac were used to test the effects of Pac on intracellular lipid metabolism. Molecular docking studies were performed to explore the potential targets of Pac in defending against lipid deposition. MPHs isolated from liver-specific SIRT6-deficient mice were subjected to OA + PA incubation and treated with Pac to determine the function and detailed mechanism. It was revealed that Pac activated SIRT6 by increasing its expression and deacetylase activity. Pa prevented OA + PA-induced lipid deposition in MPHs in a dose-dependent manner. Pac (50 µM) administration significantly reduced TG accumulation and increased fatty acid oxidation rate in OA + PA-incubated MPHs. Meanwhile, as per the results of molecular docking and relative mRNA levels, Pac activated SIRT6 and increased SIRT6 deacetylation levels. Furthermore, SIRT6 deletions in MPHs abolished the protective effects of Pac against OA + PA-induced hepatocyte lipid metabolism disorders. The present study demonstrated that Pac alleviates OA + PA-induced hepatocyte lipid metabolism disorders by activating SIRT6 signaling. Overall, SIRT6 signaling increases oxidative stress burden and promotes hepatocyte lipolysis. |
format | Online Article Text |
id | pubmed-10236048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-102360482023-06-03 Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders Pan, Zhi-Sen Chen, Yan-Ling Tang, Kai-Jia Liu, Zhang-Zhou Liang, Jia-Li Guan, Yan-Hao Xin, Xiao-Yi Liu, Chang-Hui Shen, Chuang-Peng Exp Ther Med Articles Pachymic acid (Pac), a major bioactive constituent of Poria cocos, is an antioxidant that inhibits triglyceride (TG) accumulation. To the best of our knowledge, the present study investigated for the first time whether Pac activated sirtuin 6 (SIRT6) signaling to alleviate oleic acid (OA)-palmitic acid (PA)-induced lipid metabolism disorders in mouse primary hepatocytes (MPHs). In the present study, MPHs challenged with Pac were used to test the effects of Pac on intracellular lipid metabolism. Molecular docking studies were performed to explore the potential targets of Pac in defending against lipid deposition. MPHs isolated from liver-specific SIRT6-deficient mice were subjected to OA + PA incubation and treated with Pac to determine the function and detailed mechanism. It was revealed that Pac activated SIRT6 by increasing its expression and deacetylase activity. Pa prevented OA + PA-induced lipid deposition in MPHs in a dose-dependent manner. Pac (50 µM) administration significantly reduced TG accumulation and increased fatty acid oxidation rate in OA + PA-incubated MPHs. Meanwhile, as per the results of molecular docking and relative mRNA levels, Pac activated SIRT6 and increased SIRT6 deacetylation levels. Furthermore, SIRT6 deletions in MPHs abolished the protective effects of Pac against OA + PA-induced hepatocyte lipid metabolism disorders. The present study demonstrated that Pac alleviates OA + PA-induced hepatocyte lipid metabolism disorders by activating SIRT6 signaling. Overall, SIRT6 signaling increases oxidative stress burden and promotes hepatocyte lipolysis. D.A. Spandidos 2023-05-15 /pmc/articles/PMC10236048/ /pubmed/37273757 http://dx.doi.org/10.3892/etm.2023.12019 Text en Copyright: © Pan et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Pan, Zhi-Sen Chen, Yan-Ling Tang, Kai-Jia Liu, Zhang-Zhou Liang, Jia-Li Guan, Yan-Hao Xin, Xiao-Yi Liu, Chang-Hui Shen, Chuang-Peng Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders |
title | Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders |
title_full | Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders |
title_fullStr | Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders |
title_full_unstemmed | Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders |
title_short | Pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders |
title_sort | pachymic acid modulates sirtuin 6 activity to alleviate lipid metabolism disorders |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10236048/ https://www.ncbi.nlm.nih.gov/pubmed/37273757 http://dx.doi.org/10.3892/etm.2023.12019 |
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