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Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice

Glycolipid metabolic disorder is a serious threat to human health. Dark tea is a kind of traditional Chinese tea, which may regulate the glycolipid metabolic disorders. Dark tea extract (DTE) is the water extraction obtained from dark tea. Compared with traditional dark tea, DTE has the benefits of...

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Autores principales: Wang, Caiqiong, Hu, Minghai, Yi, Yuhang, Wen, Xinnian, Lv, Chenghao, Shi, Meng, Zeng, Chaoxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9514424/
https://www.ncbi.nlm.nih.gov/pubmed/36176635
http://dx.doi.org/10.3389/fnut.2022.1006517
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author Wang, Caiqiong
Hu, Minghai
Yi, Yuhang
Wen, Xinnian
Lv, Chenghao
Shi, Meng
Zeng, Chaoxi
author_facet Wang, Caiqiong
Hu, Minghai
Yi, Yuhang
Wen, Xinnian
Lv, Chenghao
Shi, Meng
Zeng, Chaoxi
author_sort Wang, Caiqiong
collection PubMed
description Glycolipid metabolic disorder is a serious threat to human health. Dark tea is a kind of traditional Chinese tea, which may regulate the glycolipid metabolic disorders. Dark tea extract (DTE) is the water extraction obtained from dark tea. Compared with traditional dark tea, DTE has the benefits of convenient consumption and greater potential for promoting health. However, the regulation of DTE on glycolipid metabolism and its molecular mechanism is rarely investigated. In our study, DTE was used as raw material to study the effect and molecular mechanism of its intervention on the glycolipid metabolic in db/db diabetic mice by using multiomics analysis and modern biological techniques. (1) DTE could significantly reduce fasting glucose in diabetic db/db mice, and the higher dose group has a better effect. Histopathological examination showed that DTE slightly improve the number of islets and decrease the number of islet β cells in the pancreatic tissue in db/db mice. (2) RNA-Seq was used to analyze the gene expression in liver tissue. In terms of biological processes, DTE mainly affected the inflammation and fatty acid metabolism. In terms of cell components, the lipoprotein and respiratory chain are mainly affected. In the aspect of molecular function, DTE mainly affected the redox related enzyme activity, iron ion binding and glutathione transferase. Arachidonic acid metabolism pathway, glutathione metabolism and PPAR signaling pathway were enriched by DTE with the results of KEGG pathway enrichment. In addition, real-time PCR results confirmed that DTE could significantly activate key genes of PPAR signaling pathway like Fabp1, Cyp4a1, Ehhadh, Cyp4a32, Aqp7 and Me1. (3) 16s rDNA showed that DTE could significantly decrease the ratio of Firmicutes/Bacteroidetes and the abundance of Proteobacteria, and increased the relative abundance of Verrucomicrobia at the phylum level. At the genus level, the relative abundance of Akkermansia, Prevotellaceae, Bacteroides and Alloprevotella was significantly increased after DTE treatment. This study provides multiomics molecular evidence for the intervention effect of DTE on abnormal glucose and lipid metabolism and the application of precise nutritional diet intervention of dark tea extract.
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spelling pubmed-95144242022-09-28 Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice Wang, Caiqiong Hu, Minghai Yi, Yuhang Wen, Xinnian Lv, Chenghao Shi, Meng Zeng, Chaoxi Front Nutr Nutrition Glycolipid metabolic disorder is a serious threat to human health. Dark tea is a kind of traditional Chinese tea, which may regulate the glycolipid metabolic disorders. Dark tea extract (DTE) is the water extraction obtained from dark tea. Compared with traditional dark tea, DTE has the benefits of convenient consumption and greater potential for promoting health. However, the regulation of DTE on glycolipid metabolism and its molecular mechanism is rarely investigated. In our study, DTE was used as raw material to study the effect and molecular mechanism of its intervention on the glycolipid metabolic in db/db diabetic mice by using multiomics analysis and modern biological techniques. (1) DTE could significantly reduce fasting glucose in diabetic db/db mice, and the higher dose group has a better effect. Histopathological examination showed that DTE slightly improve the number of islets and decrease the number of islet β cells in the pancreatic tissue in db/db mice. (2) RNA-Seq was used to analyze the gene expression in liver tissue. In terms of biological processes, DTE mainly affected the inflammation and fatty acid metabolism. In terms of cell components, the lipoprotein and respiratory chain are mainly affected. In the aspect of molecular function, DTE mainly affected the redox related enzyme activity, iron ion binding and glutathione transferase. Arachidonic acid metabolism pathway, glutathione metabolism and PPAR signaling pathway were enriched by DTE with the results of KEGG pathway enrichment. In addition, real-time PCR results confirmed that DTE could significantly activate key genes of PPAR signaling pathway like Fabp1, Cyp4a1, Ehhadh, Cyp4a32, Aqp7 and Me1. (3) 16s rDNA showed that DTE could significantly decrease the ratio of Firmicutes/Bacteroidetes and the abundance of Proteobacteria, and increased the relative abundance of Verrucomicrobia at the phylum level. At the genus level, the relative abundance of Akkermansia, Prevotellaceae, Bacteroides and Alloprevotella was significantly increased after DTE treatment. This study provides multiomics molecular evidence for the intervention effect of DTE on abnormal glucose and lipid metabolism and the application of precise nutritional diet intervention of dark tea extract. Frontiers Media S.A. 2022-09-08 /pmc/articles/PMC9514424/ /pubmed/36176635 http://dx.doi.org/10.3389/fnut.2022.1006517 Text en Copyright © 2022 Wang, Hu, Yi, Wen, Lv, Shi and Zeng. 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 Nutrition
Wang, Caiqiong
Hu, Minghai
Yi, Yuhang
Wen, Xinnian
Lv, Chenghao
Shi, Meng
Zeng, Chaoxi
Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice
title Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice
title_full Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice
title_fullStr Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice
title_full_unstemmed Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice
title_short Multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice
title_sort multiomic analysis of dark tea extract on glycolipid metabolic disorders in db/db mice
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9514424/
https://www.ncbi.nlm.nih.gov/pubmed/36176635
http://dx.doi.org/10.3389/fnut.2022.1006517
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