Cargando…
Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice
OBJECTIVE: The incidence of non-alcoholic fatty liver disease is increasing every year, and there is growing evidence that metabolites and intestinal bacteria play a causal role in NAFLD. Gentiopicroside, a major iridoids compound in gentian, has been reported to reduce hepatic lipid accumulation. H...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443917/ https://www.ncbi.nlm.nih.gov/pubmed/37614606 http://dx.doi.org/10.3389/fmicb.2023.1145430 |
_version_ | 1785093944621662208 |
---|---|
author | Wang, Lijuan Jiang, Yuxin Yu, Qian Xiao, Chunping Sun, Jin Weng, Lili Qiu, Ye |
author_facet | Wang, Lijuan Jiang, Yuxin Yu, Qian Xiao, Chunping Sun, Jin Weng, Lili Qiu, Ye |
author_sort | Wang, Lijuan |
collection | PubMed |
description | OBJECTIVE: The incidence of non-alcoholic fatty liver disease is increasing every year, and there is growing evidence that metabolites and intestinal bacteria play a causal role in NAFLD. Gentiopicroside, a major iridoids compound in gentian, has been reported to reduce hepatic lipid accumulation. However to date, no studies have confirmed whether the predominance of Gentiopicroside is related to metabolites and intestinal bacteria. Therefore, we sought to study whether the hypolipidemic effect of Gentiopicroside is related to metabolic function and intestinal flora regulation. METHODS: In the present study, C57BL/6J mice were fed a high-fat diet for 12 weeks, followed by a high-fat diet with or without Gentiopicroside for 8 weeks, respectively. The Gentiopicroside intervention reduced body weight gain, liver index, and decreased serum biochemical parameters such as alanine aminotransferase, aspartate aminotransferase, and triglycerides in high-fat fed mice. The effect of Gentiopicroside on non-alcoholic fatty liver disease was studied using serum untargeted metabolomics and 16S rDNA assay. RESULTS: Metabolomic analysis showed that the addition of Gentiopicroside significantly altered the levels of amino acids, unmetabolized Gentiopicroside after administration, and metabolites such as Cinnoline, Galabiosylceramide, and Tryptophyl-Tyrosine, which are involved in the pathways regulating bile secretion, tryptophan metabolism, and lipid metabolism. Analysis of intestinal bacteria showed that Gentiopicrosides altered the community composition structure of intestinal bacteria, characterized by an increase and a decrease in beneficial and harmful bacteria, respectively. In addition, correlation analysis showed that the effect of Gentiopicroside on metabolites was positively correlated with intestinal flora Bacteroides, Lactobacillus, Muribaculum, and Prevotellaceae_UCG_001. Finally, the combined analysis revealed that metabolites were associated with the regulation of Firmicutes and Actinobacteria and positively correlated with lipid levels. CONCLUSION: These results suggest that Gentiopicroside may be a potential agent for the prevention of intestinal disorders and the alleviation of non-alcoholic fatty liver disease. |
format | Online Article Text |
id | pubmed-10443917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104439172023-08-23 Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice Wang, Lijuan Jiang, Yuxin Yu, Qian Xiao, Chunping Sun, Jin Weng, Lili Qiu, Ye Front Microbiol Microbiology OBJECTIVE: The incidence of non-alcoholic fatty liver disease is increasing every year, and there is growing evidence that metabolites and intestinal bacteria play a causal role in NAFLD. Gentiopicroside, a major iridoids compound in gentian, has been reported to reduce hepatic lipid accumulation. However to date, no studies have confirmed whether the predominance of Gentiopicroside is related to metabolites and intestinal bacteria. Therefore, we sought to study whether the hypolipidemic effect of Gentiopicroside is related to metabolic function and intestinal flora regulation. METHODS: In the present study, C57BL/6J mice were fed a high-fat diet for 12 weeks, followed by a high-fat diet with or without Gentiopicroside for 8 weeks, respectively. The Gentiopicroside intervention reduced body weight gain, liver index, and decreased serum biochemical parameters such as alanine aminotransferase, aspartate aminotransferase, and triglycerides in high-fat fed mice. The effect of Gentiopicroside on non-alcoholic fatty liver disease was studied using serum untargeted metabolomics and 16S rDNA assay. RESULTS: Metabolomic analysis showed that the addition of Gentiopicroside significantly altered the levels of amino acids, unmetabolized Gentiopicroside after administration, and metabolites such as Cinnoline, Galabiosylceramide, and Tryptophyl-Tyrosine, which are involved in the pathways regulating bile secretion, tryptophan metabolism, and lipid metabolism. Analysis of intestinal bacteria showed that Gentiopicrosides altered the community composition structure of intestinal bacteria, characterized by an increase and a decrease in beneficial and harmful bacteria, respectively. In addition, correlation analysis showed that the effect of Gentiopicroside on metabolites was positively correlated with intestinal flora Bacteroides, Lactobacillus, Muribaculum, and Prevotellaceae_UCG_001. Finally, the combined analysis revealed that metabolites were associated with the regulation of Firmicutes and Actinobacteria and positively correlated with lipid levels. CONCLUSION: These results suggest that Gentiopicroside may be a potential agent for the prevention of intestinal disorders and the alleviation of non-alcoholic fatty liver disease. Frontiers Media S.A. 2023-08-08 /pmc/articles/PMC10443917/ /pubmed/37614606 http://dx.doi.org/10.3389/fmicb.2023.1145430 Text en Copyright © 2023 Wang, Jiang, Yu, Xiao, Sun, Weng and Qiu. https://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 | Microbiology Wang, Lijuan Jiang, Yuxin Yu, Qian Xiao, Chunping Sun, Jin Weng, Lili Qiu, Ye Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice |
title | Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice |
title_full | Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice |
title_fullStr | Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice |
title_full_unstemmed | Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice |
title_short | Gentiopicroside improves high-fat diet-induced NAFLD in association with modulation of host serum metabolome and gut microbiome in mice |
title_sort | gentiopicroside improves high-fat diet-induced nafld in association with modulation of host serum metabolome and gut microbiome in mice |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443917/ https://www.ncbi.nlm.nih.gov/pubmed/37614606 http://dx.doi.org/10.3389/fmicb.2023.1145430 |
work_keys_str_mv | AT wanglijuan gentiopicrosideimproveshighfatdietinducednafldinassociationwithmodulationofhostserummetabolomeandgutmicrobiomeinmice AT jiangyuxin gentiopicrosideimproveshighfatdietinducednafldinassociationwithmodulationofhostserummetabolomeandgutmicrobiomeinmice AT yuqian gentiopicrosideimproveshighfatdietinducednafldinassociationwithmodulationofhostserummetabolomeandgutmicrobiomeinmice AT xiaochunping gentiopicrosideimproveshighfatdietinducednafldinassociationwithmodulationofhostserummetabolomeandgutmicrobiomeinmice AT sunjin gentiopicrosideimproveshighfatdietinducednafldinassociationwithmodulationofhostserummetabolomeandgutmicrobiomeinmice AT wenglili gentiopicrosideimproveshighfatdietinducednafldinassociationwithmodulationofhostserummetabolomeandgutmicrobiomeinmice AT qiuye gentiopicrosideimproveshighfatdietinducednafldinassociationwithmodulationofhostserummetabolomeandgutmicrobiomeinmice |