Cargando…

Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis

INTRODUCTION: Non-alcoholic fatty liver disease (NAFLD) with obesity seriously threats public health. Our previous studies showed that dark tea had more potential on regulating lipid metabolism than other teas, and theabrownin (TB) was considered to be a main contributor to the bioactivity of dark t...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Hang-Yu, Huang, Si-Yu, Zhou, Dan-Dan, Xiong, Ruo-Gu, Luo, Min, Saimaiti, Adila, Han, Mu-Ke, Gan, Ren-You, Zhu, Hui-Lian, Li, Hua-Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555776/
https://www.ncbi.nlm.nih.gov/pubmed/36639024
http://dx.doi.org/10.1016/j.jare.2023.01.008
_version_ 1785116732568895488
author Li, Hang-Yu
Huang, Si-Yu
Zhou, Dan-Dan
Xiong, Ruo-Gu
Luo, Min
Saimaiti, Adila
Han, Mu-Ke
Gan, Ren-You
Zhu, Hui-Lian
Li, Hua-Bin
author_facet Li, Hang-Yu
Huang, Si-Yu
Zhou, Dan-Dan
Xiong, Ruo-Gu
Luo, Min
Saimaiti, Adila
Han, Mu-Ke
Gan, Ren-You
Zhu, Hui-Lian
Li, Hua-Bin
author_sort Li, Hang-Yu
collection PubMed
description INTRODUCTION: Non-alcoholic fatty liver disease (NAFLD) with obesity seriously threats public health. Our previous studies showed that dark tea had more potential on regulating lipid metabolism than other teas, and theabrownin (TB) was considered to be a main contributor to the bioactivity of dark tea. OBJECTIVES: This in vivo study aims to reveal the effects and molecular mechanisms of TB on NAFLD and obesity, and the role of the gut-liver axis is explored. METHODS: The histopathological examinations, biochemical tests, and nuclear magnetic resonance were applied to evaluate the effects of TB on NAFLD and obesity. The untargeted metabolomics was used to find the key molecule for further exploration of molecular mechanisms. The 16S rRNA gene sequencing was used to assess the changes in gut microbiota. The antibiotic cocktail and fecal microbiota transplant were used to clarify the role of gut microbiota. RESULTS: TB markedly reduced body weight gain (67.01%), body fat rate (62.81%), and hepatic TG level (51.35%) in the preventive experiment. Especially, TB decreased body weight (32.16%), body fat rate (42.56%), and hepatic TG level (42.86%) in the therapeutic experiment. The mechanisms of action could be the improvement of fatty acid oxidation, lipolysis, and oxidative stress via the regulation of serotonin-related signaling pathways. Also, TB increased the abundance of serotonin-related gut microbiota, such as Akkermansia, Bacteroides and Parabacteroides. Antibiotics-induced gut bacterial dysbiosis disrupted the regulation of TB on serotonin-related signaling pathways in liver, whereas the beneficial regulation of TB on target proteins was regained with the restoration of gut microbiota. CONCLUSION: We find that TB has markedly preventive and therapeutic effects on NAFLD and obesity by regulating serotonin level and related signaling pathways through gut microbiota. Furthermore, gut microbiota and TB co-contribute to alleviating NAFLD and obesity. TB could be a promising medicine for NAFLD and obesity.
format Online
Article
Text
id pubmed-10555776
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-105557762023-10-07 Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis Li, Hang-Yu Huang, Si-Yu Zhou, Dan-Dan Xiong, Ruo-Gu Luo, Min Saimaiti, Adila Han, Mu-Ke Gan, Ren-You Zhu, Hui-Lian Li, Hua-Bin J Adv Res Original Article INTRODUCTION: Non-alcoholic fatty liver disease (NAFLD) with obesity seriously threats public health. Our previous studies showed that dark tea had more potential on regulating lipid metabolism than other teas, and theabrownin (TB) was considered to be a main contributor to the bioactivity of dark tea. OBJECTIVES: This in vivo study aims to reveal the effects and molecular mechanisms of TB on NAFLD and obesity, and the role of the gut-liver axis is explored. METHODS: The histopathological examinations, biochemical tests, and nuclear magnetic resonance were applied to evaluate the effects of TB on NAFLD and obesity. The untargeted metabolomics was used to find the key molecule for further exploration of molecular mechanisms. The 16S rRNA gene sequencing was used to assess the changes in gut microbiota. The antibiotic cocktail and fecal microbiota transplant were used to clarify the role of gut microbiota. RESULTS: TB markedly reduced body weight gain (67.01%), body fat rate (62.81%), and hepatic TG level (51.35%) in the preventive experiment. Especially, TB decreased body weight (32.16%), body fat rate (42.56%), and hepatic TG level (42.86%) in the therapeutic experiment. The mechanisms of action could be the improvement of fatty acid oxidation, lipolysis, and oxidative stress via the regulation of serotonin-related signaling pathways. Also, TB increased the abundance of serotonin-related gut microbiota, such as Akkermansia, Bacteroides and Parabacteroides. Antibiotics-induced gut bacterial dysbiosis disrupted the regulation of TB on serotonin-related signaling pathways in liver, whereas the beneficial regulation of TB on target proteins was regained with the restoration of gut microbiota. CONCLUSION: We find that TB has markedly preventive and therapeutic effects on NAFLD and obesity by regulating serotonin level and related signaling pathways through gut microbiota. Furthermore, gut microbiota and TB co-contribute to alleviating NAFLD and obesity. TB could be a promising medicine for NAFLD and obesity. Elsevier 2023-01-11 /pmc/articles/PMC10555776/ /pubmed/36639024 http://dx.doi.org/10.1016/j.jare.2023.01.008 Text en © 2023 The Authors. Published by Elsevier B.V. on behalf of Cairo University. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Li, Hang-Yu
Huang, Si-Yu
Zhou, Dan-Dan
Xiong, Ruo-Gu
Luo, Min
Saimaiti, Adila
Han, Mu-Ke
Gan, Ren-You
Zhu, Hui-Lian
Li, Hua-Bin
Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis
title Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis
title_full Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis
title_fullStr Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis
title_full_unstemmed Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis
title_short Theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis
title_sort theabrownin inhibits obesity and non-alcoholic fatty liver disease in mice via serotonin-related signaling pathways and gut-liver axis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555776/
https://www.ncbi.nlm.nih.gov/pubmed/36639024
http://dx.doi.org/10.1016/j.jare.2023.01.008
work_keys_str_mv AT lihangyu theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT huangsiyu theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT zhoudandan theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT xiongruogu theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT luomin theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT saimaitiadila theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT hanmuke theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT ganrenyou theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT zhuhuilian theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis
AT lihuabin theabrownininhibitsobesityandnonalcoholicfattyliverdiseaseinmiceviaserotoninrelatedsignalingpathwaysandgutliveraxis