Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola Bunting

Abstract Background Bile acids and gut microbiota participate in the pathogenesis of liver fibrosis (LF). The total alkaloids of Corydalis saxicola Bunting (TACS) is a traditional Chinese medicine extract that has been used to treat LF, but the underlying mechanisms are not clear. This study perform...

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Main Authors: Qianyi Wang, MeiLing Zhang, Mingwei Meng, Zhuo Luo, Ziping Pan, Lijun Deng, Jinghua Qin, Bingjian Guo, Dan Zhu, Yanmin Zhang, Hongwei Guo, Yonghong Liang, Zhiheng Su
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Language:English
Published: BMC 2025-07-01
Series:Chinese Medicine
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Online Access:https://doi.org/10.1186/s13020-025-01158-2
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author Qianyi Wang
MeiLing Zhang
Mingwei Meng
Zhuo Luo
Ziping Pan
Lijun Deng
Jinghua Qin
Bingjian Guo
Dan Zhu
Yanmin Zhang
Hongwei Guo
Yonghong Liang
Zhiheng Su
author_facet Qianyi Wang
MeiLing Zhang
Mingwei Meng
Zhuo Luo
Ziping Pan
Lijun Deng
Jinghua Qin
Bingjian Guo
Dan Zhu
Yanmin Zhang
Hongwei Guo
Yonghong Liang
Zhiheng Su
author_sort Qianyi Wang
collection DOAJ
description Abstract Background Bile acids and gut microbiota participate in the pathogenesis of liver fibrosis (LF). The total alkaloids of Corydalis saxicola Bunting (TACS) is a traditional Chinese medicine extract that has been used to treat LF, but the underlying mechanisms are not clear. This study performed integrated metabolomics and gut microbiome analysis to study the anti-LF mechanism of TACS using a rat model. Methods Ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) was used to identify the chemical compounds in TACS. Biochemical and histopathological analysis were performed to determine the efficacy of TACS. Bile acid-targeted metabolomics was used to assess changes in the bile acid (BA) profiles in TACS-treated LF rats. 16S rRNA gene sequencing and metagenomics were used to assess changes in the gut microbiota of the TACS-treated LF rats. Antibiotic cocktail treatment and fecal microbiota transplantation (FMT) were used to determine the relationship between the gut microbiota and the anti-LF effects of TACS. Metagenomics was used to identify significantly enriched gut microbiota after TACS treatment and its correlation with the anti-LF effects was verified by in vivo experiments. Results TACS treatment significantly reduced the levels of serum liver enzymes, fibrosis and pro-inflammatory cytokines in the liver. TACS significantly increased the levels of chenodeoxycholic acid (CDCA) and taurochenodeoxycholic acid (TCDCA) in the cecum and decreased the levels of cholic acid (CA) and deoxycholic acid (DCA) in the liver of the LF rats. TACS significantly increased the abundances of Lactobacillus and Akkermansia in the LF rats. Antibiotic cocktail treatment and FMT have shown that the effect of TACS cure liver fibrosis depends on the gut microbiota. The abundance of Lactobacillus reuteri was significantly increased by TACS. Administration of Lactobacillus reuteri via gavage ameliorated LF. Conclusions TACS exerted anti-LF effects in rats by modulating bile acid metabolism and gut microbiome. Graphical Abstract
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spelling doaj-art-40bfd263b27d447e998a6fc18c0ab2ae2025-08-20T03:45:36ZengBMCChinese Medicine1749-85462025-07-0120111710.1186/s13020-025-01158-2Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola BuntingQianyi Wang0MeiLing Zhang1Mingwei Meng2Zhuo Luo3Ziping Pan4Lijun Deng5Jinghua Qin6Bingjian Guo7Dan Zhu8Yanmin Zhang9Hongwei Guo10Yonghong Liang11Zhiheng Su12Department of Pharmacy, Guangxi Medical University Cancer HospitalPharmaceutical College, Guangxi Medical UniversityThe First People’s Hospital of Nanning, The Fifth Affiliated Hospital of Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversitySchool of Pharmacy, Health Science Center, Xian Jiao Tong UniversityPharmaceutical College, Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversityPharmaceutical College, Guangxi Medical UniversityAbstract Background Bile acids and gut microbiota participate in the pathogenesis of liver fibrosis (LF). The total alkaloids of Corydalis saxicola Bunting (TACS) is a traditional Chinese medicine extract that has been used to treat LF, but the underlying mechanisms are not clear. This study performed integrated metabolomics and gut microbiome analysis to study the anti-LF mechanism of TACS using a rat model. Methods Ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) was used to identify the chemical compounds in TACS. Biochemical and histopathological analysis were performed to determine the efficacy of TACS. Bile acid-targeted metabolomics was used to assess changes in the bile acid (BA) profiles in TACS-treated LF rats. 16S rRNA gene sequencing and metagenomics were used to assess changes in the gut microbiota of the TACS-treated LF rats. Antibiotic cocktail treatment and fecal microbiota transplantation (FMT) were used to determine the relationship between the gut microbiota and the anti-LF effects of TACS. Metagenomics was used to identify significantly enriched gut microbiota after TACS treatment and its correlation with the anti-LF effects was verified by in vivo experiments. Results TACS treatment significantly reduced the levels of serum liver enzymes, fibrosis and pro-inflammatory cytokines in the liver. TACS significantly increased the levels of chenodeoxycholic acid (CDCA) and taurochenodeoxycholic acid (TCDCA) in the cecum and decreased the levels of cholic acid (CA) and deoxycholic acid (DCA) in the liver of the LF rats. TACS significantly increased the abundances of Lactobacillus and Akkermansia in the LF rats. Antibiotic cocktail treatment and FMT have shown that the effect of TACS cure liver fibrosis depends on the gut microbiota. The abundance of Lactobacillus reuteri was significantly increased by TACS. Administration of Lactobacillus reuteri via gavage ameliorated LF. Conclusions TACS exerted anti-LF effects in rats by modulating bile acid metabolism and gut microbiome. Graphical Abstracthttps://doi.org/10.1186/s13020-025-01158-2Total alkaloids of Corydalis saxicola BuntingLiver fibrosisBile acidGut microbiotaFecal microbiota transplantationLactobacillus reuteri
spellingShingle Qianyi Wang
MeiLing Zhang
Mingwei Meng
Zhuo Luo
Ziping Pan
Lijun Deng
Jinghua Qin
Bingjian Guo
Dan Zhu
Yanmin Zhang
Hongwei Guo
Yonghong Liang
Zhiheng Su
Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola Bunting
Chinese Medicine
Total alkaloids of Corydalis saxicola Bunting
Liver fibrosis
Bile acid
Gut microbiota
Fecal microbiota transplantation
Lactobacillus reuteri
title Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola Bunting
title_full Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola Bunting
title_fullStr Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola Bunting
title_full_unstemmed Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola Bunting
title_short Integration bile acid metabolomics and gut microbiome to study the anti-liver fibrosis effects of total alkaloids of Corydalis saxicola Bunting
title_sort integration bile acid metabolomics and gut microbiome to study the anti liver fibrosis effects of total alkaloids of corydalis saxicola bunting
topic Total alkaloids of Corydalis saxicola Bunting
Liver fibrosis
Bile acid
Gut microbiota
Fecal microbiota transplantation
Lactobacillus reuteri
url https://doi.org/10.1186/s13020-025-01158-2
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