Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease

Nonalcoholic fatty liver disease (NAFLD) has become one of the most prominent causes of chronic liver diseases and malignancies. However, few therapy has been approved. Radix Bupleuri (RB) is the most frequently used herbal medicine for the treatment of liver diseases. In the current study, we aim t...

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Autores principales: Xiaojiaoyang Li, Junde Ge, Yajing Li, Yajie Cai, Qi Zheng, Nana Huang, Yiqing Gu, Qi Han, Yunqian Li, Rong Sun, Runping Liu
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Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/cb0a8cdb81264de8a6e3c5022eec608a
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spelling oai:doaj.org-article:cb0a8cdb81264de8a6e3c5022eec608a2021-12-02T05:01:20ZIntegrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease2211-383510.1016/j.apsb.2021.03.018https://doaj.org/article/cb0a8cdb81264de8a6e3c5022eec608a2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2211383521000897https://doaj.org/toc/2211-3835Nonalcoholic fatty liver disease (NAFLD) has become one of the most prominent causes of chronic liver diseases and malignancies. However, few therapy has been approved. Radix Bupleuri (RB) is the most frequently used herbal medicine for the treatment of liver diseases. In the current study, we aim to systemically evaluate the therapeutic effects of saikosaponin A (SSa) and saikosaponin D (SSd), the major bioactive monomers in RB, against NAFLD and to investigate the underlying mechanisms. Our results demonstrated that both SSa and SSd improved diet-induced NAFLD. Integrative lipidomic and transcriptomic analysis revealed that SSa and SSd modulated glycerolipid metabolism by regulating related genes, like Lipe and Lipg. SSd profoundly suppressed the fatty acid biosynthesis by downregulating Fasn and Acaca expression and promoted fatty acid degradation by inducing Acox1 and Cpt1a expression. Bioinformatic analysis further predicted the implication of master transcription factors, including peroxisome proliferator-activated receptor alpha (PPARα), in the protective effects of SSa and SSd. These results were further confirmed in vitro in mouse primary hepatocytes. In summary, our study uncoded the complicated mechanisms underlying the promising anti-steatosis activities of saikosaponins (SSs), and provided critical evidence inspiring the discovery of innovative therapies based on SSa and SSd for the treatment of NAFLD and related complications.Xiaojiaoyang LiJunde GeYajing LiYajie CaiQi ZhengNana HuangYiqing GuQi HanYunqian LiRong SunRunping LiuElsevierarticleSaikosaponinNonalcoholic fatty liver diseaseLipidomeTranscriptomeLipid metabolismTherapeutics. PharmacologyRM1-950ENActa Pharmaceutica Sinica B, Vol 11, Iss 11, Pp 3527-3541 (2021)
institution DOAJ
collection DOAJ
language EN
topic Saikosaponin
Nonalcoholic fatty liver disease
Lipidome
Transcriptome
Lipid metabolism
Therapeutics. Pharmacology
RM1-950
spellingShingle Saikosaponin
Nonalcoholic fatty liver disease
Lipidome
Transcriptome
Lipid metabolism
Therapeutics. Pharmacology
RM1-950
Xiaojiaoyang Li
Junde Ge
Yajing Li
Yajie Cai
Qi Zheng
Nana Huang
Yiqing Gu
Qi Han
Yunqian Li
Rong Sun
Runping Liu
Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease
description Nonalcoholic fatty liver disease (NAFLD) has become one of the most prominent causes of chronic liver diseases and malignancies. However, few therapy has been approved. Radix Bupleuri (RB) is the most frequently used herbal medicine for the treatment of liver diseases. In the current study, we aim to systemically evaluate the therapeutic effects of saikosaponin A (SSa) and saikosaponin D (SSd), the major bioactive monomers in RB, against NAFLD and to investigate the underlying mechanisms. Our results demonstrated that both SSa and SSd improved diet-induced NAFLD. Integrative lipidomic and transcriptomic analysis revealed that SSa and SSd modulated glycerolipid metabolism by regulating related genes, like Lipe and Lipg. SSd profoundly suppressed the fatty acid biosynthesis by downregulating Fasn and Acaca expression and promoted fatty acid degradation by inducing Acox1 and Cpt1a expression. Bioinformatic analysis further predicted the implication of master transcription factors, including peroxisome proliferator-activated receptor alpha (PPARα), in the protective effects of SSa and SSd. These results were further confirmed in vitro in mouse primary hepatocytes. In summary, our study uncoded the complicated mechanisms underlying the promising anti-steatosis activities of saikosaponins (SSs), and provided critical evidence inspiring the discovery of innovative therapies based on SSa and SSd for the treatment of NAFLD and related complications.
format article
author Xiaojiaoyang Li
Junde Ge
Yajing Li
Yajie Cai
Qi Zheng
Nana Huang
Yiqing Gu
Qi Han
Yunqian Li
Rong Sun
Runping Liu
author_facet Xiaojiaoyang Li
Junde Ge
Yajing Li
Yajie Cai
Qi Zheng
Nana Huang
Yiqing Gu
Qi Han
Yunqian Li
Rong Sun
Runping Liu
author_sort Xiaojiaoyang Li
title Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease
title_short Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease
title_full Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease
title_fullStr Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease
title_full_unstemmed Integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins A and D on non-alcoholic fatty liver disease
title_sort integrative lipidomic and transcriptomic study unravels the therapeutic effects of saikosaponins a and d on non-alcoholic fatty liver disease
publisher Elsevier
publishDate 2021
url https://doaj.org/article/cb0a8cdb81264de8a6e3c5022eec608a
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