Cargando…
Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway
Tangshen formula (TSF), a formula of Chinese herbal medicine, improves lipid metabolism in humans and animals with diabetic kidney disease. However, the effect and mechanism of TSF on nonalcoholic fatty liver disease (NAFLD) remain unclear. The activation of autophagy appears to be a potential mecha...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498888/ https://www.ncbi.nlm.nih.gov/pubmed/31105592 http://dx.doi.org/10.3389/fphys.2019.00494 |
_version_ | 1783415700691353600 |
---|---|
author | Wang, Yan Zhao, Hailing Li, Xin Li, Nan Wang, Qian Liu, Yanzhen Liang, Qionglin Shao, Zixing Zhang, Nannan Zhao, Tingting Peng, Liang Li, Ping |
author_facet | Wang, Yan Zhao, Hailing Li, Xin Li, Nan Wang, Qian Liu, Yanzhen Liang, Qionglin Shao, Zixing Zhang, Nannan Zhao, Tingting Peng, Liang Li, Ping |
author_sort | Wang, Yan |
collection | PubMed |
description | Tangshen formula (TSF), a formula of Chinese herbal medicine, improves lipid metabolism in humans and animals with diabetic kidney disease. However, the effect and mechanism of TSF on nonalcoholic fatty liver disease (NAFLD) remain unclear. The activation of autophagy appears to be a potential mechanism for improving NAFLD. In the present study, we examined the therapeutic effect of TSF on hepatic steatosis and sought to explore whether its effect is related to activating autophagy. Here, we showed that TSF treatment significantly attenuated hepatic steatosis in both high-fat diet (HFD) and methionine choline-deficient diet (MCDD)-fed mice. Meanwhile, TSF reduced lipid accumulation in palmitate (PA)-stimulated HepG2 cells and primary mouse hepatocytes. Furthermore, TSF increased Sirtuin 1 (SIRT1) expression and promoted autophagy activation in vivo. TSF also improved PA-induced suppression of both SIRT1 expression and SIRT1-dependent autophagy, thereby alleviating intracellular lipid accumulation in vitro. In addition, TSF increased SIRT1 expression and induced autophagy in an adenosine monophosphate-activated protein kinase (AMPK)-dependent manner. Moreover, SIRT1 knockdown abolished the autophagy-inducing and lipid-lowering effects of TSF. In conclusion, TSF improved lipid accumulation and hepatic steatosis by inducing the AMPK/SIRT1 pathway-mediated autophagy. |
format | Online Article Text |
id | pubmed-6498888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64988882019-05-17 Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway Wang, Yan Zhao, Hailing Li, Xin Li, Nan Wang, Qian Liu, Yanzhen Liang, Qionglin Shao, Zixing Zhang, Nannan Zhao, Tingting Peng, Liang Li, Ping Front Physiol Physiology Tangshen formula (TSF), a formula of Chinese herbal medicine, improves lipid metabolism in humans and animals with diabetic kidney disease. However, the effect and mechanism of TSF on nonalcoholic fatty liver disease (NAFLD) remain unclear. The activation of autophagy appears to be a potential mechanism for improving NAFLD. In the present study, we examined the therapeutic effect of TSF on hepatic steatosis and sought to explore whether its effect is related to activating autophagy. Here, we showed that TSF treatment significantly attenuated hepatic steatosis in both high-fat diet (HFD) and methionine choline-deficient diet (MCDD)-fed mice. Meanwhile, TSF reduced lipid accumulation in palmitate (PA)-stimulated HepG2 cells and primary mouse hepatocytes. Furthermore, TSF increased Sirtuin 1 (SIRT1) expression and promoted autophagy activation in vivo. TSF also improved PA-induced suppression of both SIRT1 expression and SIRT1-dependent autophagy, thereby alleviating intracellular lipid accumulation in vitro. In addition, TSF increased SIRT1 expression and induced autophagy in an adenosine monophosphate-activated protein kinase (AMPK)-dependent manner. Moreover, SIRT1 knockdown abolished the autophagy-inducing and lipid-lowering effects of TSF. In conclusion, TSF improved lipid accumulation and hepatic steatosis by inducing the AMPK/SIRT1 pathway-mediated autophagy. Frontiers Media S.A. 2019-04-26 /pmc/articles/PMC6498888/ /pubmed/31105592 http://dx.doi.org/10.3389/fphys.2019.00494 Text en Copyright © 2019 Wang, Zhao, Li, Li, Wang, Liu, Liang, Shao, Zhang, Zhao, Peng and Li. http://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 | Physiology Wang, Yan Zhao, Hailing Li, Xin Li, Nan Wang, Qian Liu, Yanzhen Liang, Qionglin Shao, Zixing Zhang, Nannan Zhao, Tingting Peng, Liang Li, Ping Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway |
title | Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway |
title_full | Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway |
title_fullStr | Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway |
title_full_unstemmed | Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway |
title_short | Tangshen Formula Alleviates Hepatic Steatosis by Inducing Autophagy Through the AMPK/SIRT1 Pathway |
title_sort | tangshen formula alleviates hepatic steatosis by inducing autophagy through the ampk/sirt1 pathway |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498888/ https://www.ncbi.nlm.nih.gov/pubmed/31105592 http://dx.doi.org/10.3389/fphys.2019.00494 |
work_keys_str_mv | AT wangyan tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT zhaohailing tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT lixin tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT linan tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT wangqian tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT liuyanzhen tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT liangqionglin tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT shaozixing tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT zhangnannan tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT zhaotingting tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT pengliang tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway AT liping tangshenformulaalleviateshepaticsteatosisbyinducingautophagythroughtheampksirt1pathway |