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High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates High-Fat Diet-Induced Metabolic Disorders in Mice
[Image: see text] Obesity and overweight are associated with an increasing risk of developing health conditions and chronic non-communicable diseases, including cardiovascular diseases, cancer, musculoskeletal problems, respiratory problems, and mental health, and its prevalence is rising. Diet is o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515172/ https://www.ncbi.nlm.nih.gov/pubmed/37744823 http://dx.doi.org/10.1021/acsomega.3c04874 |
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author | Weerawatanakorn, Monthana He, Sang Chang, Chun-Han Koh, Yen-Chun Yang, Meei-Ju Pan, Min-Hsiung |
author_facet | Weerawatanakorn, Monthana He, Sang Chang, Chun-Han Koh, Yen-Chun Yang, Meei-Ju Pan, Min-Hsiung |
author_sort | Weerawatanakorn, Monthana |
collection | PubMed |
description | [Image: see text] Obesity and overweight are associated with an increasing risk of developing health conditions and chronic non-communicable diseases, including cardiovascular diseases, cancer, musculoskeletal problems, respiratory problems, and mental health, and its prevalence is rising. Diet is one of three primary lifestyle interventions. Many bioactive components in tea especially oolong tea, including flavonoids, gamma-aminobutyric acid (GABA), and caffeine were reported to show related effects in reducing the risk of obesity. However, the effects of GABA oolong tea extracts (OTEs) on high-fat diet (HFD)-induced obesity are still unclear. Therefore, this study aims to explore whether the intervention of GABA OTEs can prevent HFD-induced obesity and decipher its underlying mechanisms using male C57BL/6 J mice. The result indicated that GABA OTEs reduced leptin expression in epididymal adipose tissue and showed a protective effect on nonalcoholic fatty liver disease. It promoted thermogenesis-related protein of uncoupling protein-1 and peroxisome proliferator-activated receptor-gamma coactivator (PGC-1α), boosted lipid metabolism, and promoted fatty acid oxidation. It also reduced lipogenesis-related protein levels of sterol regulatory element binding protein, acetyl-CoA carboxylase, and fatty acid synthase and inhibited hepatic triglyceride (TG) levels. These data suggest that regular drinking of GABA oolong tea has the potential to reduce the risk of being overweight, preventing obesity development through thermogenesis, lipogenesis, and lipolysis. |
format | Online Article Text |
id | pubmed-10515172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105151722023-09-23 High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates High-Fat Diet-Induced Metabolic Disorders in Mice Weerawatanakorn, Monthana He, Sang Chang, Chun-Han Koh, Yen-Chun Yang, Meei-Ju Pan, Min-Hsiung ACS Omega [Image: see text] Obesity and overweight are associated with an increasing risk of developing health conditions and chronic non-communicable diseases, including cardiovascular diseases, cancer, musculoskeletal problems, respiratory problems, and mental health, and its prevalence is rising. Diet is one of three primary lifestyle interventions. Many bioactive components in tea especially oolong tea, including flavonoids, gamma-aminobutyric acid (GABA), and caffeine were reported to show related effects in reducing the risk of obesity. However, the effects of GABA oolong tea extracts (OTEs) on high-fat diet (HFD)-induced obesity are still unclear. Therefore, this study aims to explore whether the intervention of GABA OTEs can prevent HFD-induced obesity and decipher its underlying mechanisms using male C57BL/6 J mice. The result indicated that GABA OTEs reduced leptin expression in epididymal adipose tissue and showed a protective effect on nonalcoholic fatty liver disease. It promoted thermogenesis-related protein of uncoupling protein-1 and peroxisome proliferator-activated receptor-gamma coactivator (PGC-1α), boosted lipid metabolism, and promoted fatty acid oxidation. It also reduced lipogenesis-related protein levels of sterol regulatory element binding protein, acetyl-CoA carboxylase, and fatty acid synthase and inhibited hepatic triglyceride (TG) levels. These data suggest that regular drinking of GABA oolong tea has the potential to reduce the risk of being overweight, preventing obesity development through thermogenesis, lipogenesis, and lipolysis. American Chemical Society 2023-09-05 /pmc/articles/PMC10515172/ /pubmed/37744823 http://dx.doi.org/10.1021/acsomega.3c04874 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Weerawatanakorn, Monthana He, Sang Chang, Chun-Han Koh, Yen-Chun Yang, Meei-Ju Pan, Min-Hsiung High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates High-Fat Diet-Induced Metabolic Disorders in Mice |
title | High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates
High-Fat Diet-Induced Metabolic Disorders in Mice |
title_full | High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates
High-Fat Diet-Induced Metabolic Disorders in Mice |
title_fullStr | High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates
High-Fat Diet-Induced Metabolic Disorders in Mice |
title_full_unstemmed | High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates
High-Fat Diet-Induced Metabolic Disorders in Mice |
title_short | High Gamma-Aminobutyric Acid (GABA) Oolong Tea Alleviates
High-Fat Diet-Induced Metabolic Disorders in Mice |
title_sort | high gamma-aminobutyric acid (gaba) oolong tea alleviates
high-fat diet-induced metabolic disorders in mice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515172/ https://www.ncbi.nlm.nih.gov/pubmed/37744823 http://dx.doi.org/10.1021/acsomega.3c04874 |
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