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Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity
Hydrogen sulfide (H(2)S) is recognized as a novel gasotransmitter involved in the regulation of nervous system, cardiovascular functions, inflammatory response, gastrointestinal system, and renal function. Cystathionine β‐synthase (CBS) and cystathionine γ‐lyase (CSE) are the major enzymes responsib...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041699/ https://www.ncbi.nlm.nih.gov/pubmed/29998554 http://dx.doi.org/10.14814/phy2.13630 |
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author | Liu, Mi Deng, Mokan Su, Jiahui Lin, Yu Jia, Zhanjun Peng, Kexin Wang, Fei Yang, Tianxin |
author_facet | Liu, Mi Deng, Mokan Su, Jiahui Lin, Yu Jia, Zhanjun Peng, Kexin Wang, Fei Yang, Tianxin |
author_sort | Liu, Mi |
collection | PubMed |
description | Hydrogen sulfide (H(2)S) is recognized as a novel gasotransmitter involved in the regulation of nervous system, cardiovascular functions, inflammatory response, gastrointestinal system, and renal function. Cystathionine β‐synthase (CBS) and cystathionine γ‐lyase (CSE) are the major enzymes responsible for H(2)S production through desulfuration reactions. H(2)S is reported to play a protective role in both high‐fat diet (HFD)‐induced obese and diabetic mice. However, the synthesizing enzyme involved is not clearly elucidated. The current study was aimed to investigate the regulation of CBS and CSE in different tissues including the kidney, liver, and epididymal fat in C57BL/6 mice after a HFD (60% kcal fat) for 24 weeks. The protein and mRNA expression of CBS was specifically decreased in the kidney while CSE remained unchanged, which was further confirmed in db/db mice. In the liver, CSE expression was downregulated after HFD accompanied with unchanged CBS. Moreover, CSE expression was even upregulated in epididymal fat. The specific downregulation of renal CBS may contribute to decreased H(2)S production, which could be a pathogenic mechanism of obesity. Increased CSE/H(2)S pathway in epididymal fat possibly resulted in impaired glucose uptake and aggravated insulin resistance. In conclusion, our results revealed that CBS was selectively downregulated in both diet and gene‐induced obesity models. |
format | Online Article Text |
id | pubmed-6041699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60416992018-07-13 Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity Liu, Mi Deng, Mokan Su, Jiahui Lin, Yu Jia, Zhanjun Peng, Kexin Wang, Fei Yang, Tianxin Physiol Rep Original Research Hydrogen sulfide (H(2)S) is recognized as a novel gasotransmitter involved in the regulation of nervous system, cardiovascular functions, inflammatory response, gastrointestinal system, and renal function. Cystathionine β‐synthase (CBS) and cystathionine γ‐lyase (CSE) are the major enzymes responsible for H(2)S production through desulfuration reactions. H(2)S is reported to play a protective role in both high‐fat diet (HFD)‐induced obese and diabetic mice. However, the synthesizing enzyme involved is not clearly elucidated. The current study was aimed to investigate the regulation of CBS and CSE in different tissues including the kidney, liver, and epididymal fat in C57BL/6 mice after a HFD (60% kcal fat) for 24 weeks. The protein and mRNA expression of CBS was specifically decreased in the kidney while CSE remained unchanged, which was further confirmed in db/db mice. In the liver, CSE expression was downregulated after HFD accompanied with unchanged CBS. Moreover, CSE expression was even upregulated in epididymal fat. The specific downregulation of renal CBS may contribute to decreased H(2)S production, which could be a pathogenic mechanism of obesity. Increased CSE/H(2)S pathway in epididymal fat possibly resulted in impaired glucose uptake and aggravated insulin resistance. In conclusion, our results revealed that CBS was selectively downregulated in both diet and gene‐induced obesity models. John Wiley and Sons Inc. 2018-07-12 /pmc/articles/PMC6041699/ /pubmed/29998554 http://dx.doi.org/10.14814/phy2.13630 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Liu, Mi Deng, Mokan Su, Jiahui Lin, Yu Jia, Zhanjun Peng, Kexin Wang, Fei Yang, Tianxin Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity |
title | Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity |
title_full | Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity |
title_fullStr | Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity |
title_full_unstemmed | Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity |
title_short | Specific downregulation of cystathionine β‐synthase expression in the kidney during obesity |
title_sort | specific downregulation of cystathionine β‐synthase expression in the kidney during obesity |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041699/ https://www.ncbi.nlm.nih.gov/pubmed/29998554 http://dx.doi.org/10.14814/phy2.13630 |
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