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Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence

BACKGROUND: Lifestyle and diet play a significant role in hyperuricaemia. Accumulating evidence indicates that tea consumption is associated with hyperuricaemia and gout. However, diverse compounds in different types of tea make it quite difficult to determine the relevant molecular mechanism. Here,...

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Autores principales: Sang, Siyao, Wang, Lufei, Liang, Taotao, Su, Mingjie, Li, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479443/
https://www.ncbi.nlm.nih.gov/pubmed/36109783
http://dx.doi.org/10.1186/s13020-022-00664-x
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author Sang, Siyao
Wang, Lufei
Liang, Taotao
Su, Mingjie
Li, Hui
author_facet Sang, Siyao
Wang, Lufei
Liang, Taotao
Su, Mingjie
Li, Hui
author_sort Sang, Siyao
collection PubMed
description BACKGROUND: Lifestyle and diet play a significant role in hyperuricaemia. Accumulating evidence indicates that tea consumption is associated with hyperuricaemia and gout. However, diverse compounds in different types of tea make it quite difficult to determine the relevant molecular mechanism. Here, we compared the effects of six types of tea on hyperuricaemia induced by potassium oxonate (PO) and hypoxanthine in rats and investigated the possible underlying mechanisms. METHODS: Rats were randomly assigned to ten groups: the control, hyperuricaemia model, benzbromarone positive control, traditional Chinese medicine Simiao San positive control, green tea, yellow tea, black tea, white tea, red tea, and cyan tea treatment groups. After 21 days, uric acid (UA), xanthine oxidase (XOD), alanine aminotransferase (ALT),blood urea nitrogen (BUN), and creatinine (CRE) were assessed. Serum levels of interleukin-1β (IL-1β) were measured with an enzyme-linked immunosorbent assay. Haematoxylin–eosin staining and immunohistochemistry were used to assess liver and kidney injury. RESULTS: The levels of UA, CRE, and BUN in the treatment group were decreased to varying degrees. There was a significant reduction in UA, CRE, and BUN levels for yellow tea compared to the positive control drugs. Yellow tea suppressed XOD activity and alleviated hepatic and kidney injury. Network pharmacology and untargeted metabolomics indicated that ten yellow tea bioactive ingredients and 35 targets were responsible for preventing hyperuricaemia, which was mediated by 94 signalling pathways, including IL-1β and TNF. CONCLUSION: These findings indicate that green tea cannot reduce the serum uric acid level of hyperuricaemic rats. Yellow tea can significantly improve hyperuricaemia by regulating the inflammatory response, autophagy, and apoptosis. This study provides a potential candidate for the treatment of hyperuricaemia and a basis for selecting therapeutic tea for patients with hyperuricaemia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-022-00664-x.
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spelling pubmed-94794432022-09-17 Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence Sang, Siyao Wang, Lufei Liang, Taotao Su, Mingjie Li, Hui Chin Med Research BACKGROUND: Lifestyle and diet play a significant role in hyperuricaemia. Accumulating evidence indicates that tea consumption is associated with hyperuricaemia and gout. However, diverse compounds in different types of tea make it quite difficult to determine the relevant molecular mechanism. Here, we compared the effects of six types of tea on hyperuricaemia induced by potassium oxonate (PO) and hypoxanthine in rats and investigated the possible underlying mechanisms. METHODS: Rats were randomly assigned to ten groups: the control, hyperuricaemia model, benzbromarone positive control, traditional Chinese medicine Simiao San positive control, green tea, yellow tea, black tea, white tea, red tea, and cyan tea treatment groups. After 21 days, uric acid (UA), xanthine oxidase (XOD), alanine aminotransferase (ALT),blood urea nitrogen (BUN), and creatinine (CRE) were assessed. Serum levels of interleukin-1β (IL-1β) were measured with an enzyme-linked immunosorbent assay. Haematoxylin–eosin staining and immunohistochemistry were used to assess liver and kidney injury. RESULTS: The levels of UA, CRE, and BUN in the treatment group were decreased to varying degrees. There was a significant reduction in UA, CRE, and BUN levels for yellow tea compared to the positive control drugs. Yellow tea suppressed XOD activity and alleviated hepatic and kidney injury. Network pharmacology and untargeted metabolomics indicated that ten yellow tea bioactive ingredients and 35 targets were responsible for preventing hyperuricaemia, which was mediated by 94 signalling pathways, including IL-1β and TNF. CONCLUSION: These findings indicate that green tea cannot reduce the serum uric acid level of hyperuricaemic rats. Yellow tea can significantly improve hyperuricaemia by regulating the inflammatory response, autophagy, and apoptosis. This study provides a potential candidate for the treatment of hyperuricaemia and a basis for selecting therapeutic tea for patients with hyperuricaemia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-022-00664-x. BioMed Central 2022-09-15 /pmc/articles/PMC9479443/ /pubmed/36109783 http://dx.doi.org/10.1186/s13020-022-00664-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sang, Siyao
Wang, Lufei
Liang, Taotao
Su, Mingjie
Li, Hui
Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence
title Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence
title_full Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence
title_fullStr Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence
title_full_unstemmed Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence
title_short Potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence
title_sort potential role of tea drinking in preventing hyperuricaemia in rats: biochemical and molecular evidence
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479443/
https://www.ncbi.nlm.nih.gov/pubmed/36109783
http://dx.doi.org/10.1186/s13020-022-00664-x
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