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Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats

Taurine that conjugates with bile acid (BA) and mitochondrial-tRNA (mt-tRNA) is a conditional essential amino acid in humans, similarly to cats. To better understand the influence of acquired depletion of taurine on BA metabolism, the profiling of BAs and its intermediates, BA metabolism-enzyme expr...

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Autores principales: Miyazaki, Teruo, Sasaki, Sei-Ich, Toyoda, Atsushi, Wei, Fan-Yan, Shirai, Mutsumi, Morishita, Yukio, Ikegami, Tadashi, Tomizawa, Kazuhito, Honda, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080809/
https://www.ncbi.nlm.nih.gov/pubmed/32188916
http://dx.doi.org/10.1038/s41598-020-61821-6
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author Miyazaki, Teruo
Sasaki, Sei-Ich
Toyoda, Atsushi
Wei, Fan-Yan
Shirai, Mutsumi
Morishita, Yukio
Ikegami, Tadashi
Tomizawa, Kazuhito
Honda, Akira
author_facet Miyazaki, Teruo
Sasaki, Sei-Ich
Toyoda, Atsushi
Wei, Fan-Yan
Shirai, Mutsumi
Morishita, Yukio
Ikegami, Tadashi
Tomizawa, Kazuhito
Honda, Akira
author_sort Miyazaki, Teruo
collection PubMed
description Taurine that conjugates with bile acid (BA) and mitochondrial-tRNA (mt-tRNA) is a conditional essential amino acid in humans, similarly to cats. To better understand the influence of acquired depletion of taurine on BA metabolism, the profiling of BAs and its intermediates, BA metabolism-enzyme expression, and taurine modified mt-tRNAs were evaluated in the taurine deficient diet-supplemented cats. In the taurine depleted cats, taurine-conjugated bile acids in bile and taurine-modified mt-tRNA in liver were significantly decreased, whereas unconjugated BA in serum was markedly increased. Impaired bile acid metabolism in the liver was induced accompanied with the decreases of mitochondrial cholesterol 27-hydroxylase expression and mitochondrial activity. Consequently, total bile acid concentration in bile was significantly decreased by the low activity of mitochondrial bile acid synthesis. These results implied that the insufficient dietary taurine intake causes impaired bile acid metabolism, and in turn, a risk for the various diseases similar to the mitochondrial diseases would be enhanced.
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spelling pubmed-70808092020-03-23 Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats Miyazaki, Teruo Sasaki, Sei-Ich Toyoda, Atsushi Wei, Fan-Yan Shirai, Mutsumi Morishita, Yukio Ikegami, Tadashi Tomizawa, Kazuhito Honda, Akira Sci Rep Article Taurine that conjugates with bile acid (BA) and mitochondrial-tRNA (mt-tRNA) is a conditional essential amino acid in humans, similarly to cats. To better understand the influence of acquired depletion of taurine on BA metabolism, the profiling of BAs and its intermediates, BA metabolism-enzyme expression, and taurine modified mt-tRNAs were evaluated in the taurine deficient diet-supplemented cats. In the taurine depleted cats, taurine-conjugated bile acids in bile and taurine-modified mt-tRNA in liver were significantly decreased, whereas unconjugated BA in serum was markedly increased. Impaired bile acid metabolism in the liver was induced accompanied with the decreases of mitochondrial cholesterol 27-hydroxylase expression and mitochondrial activity. Consequently, total bile acid concentration in bile was significantly decreased by the low activity of mitochondrial bile acid synthesis. These results implied that the insufficient dietary taurine intake causes impaired bile acid metabolism, and in turn, a risk for the various diseases similar to the mitochondrial diseases would be enhanced. Nature Publishing Group UK 2020-03-18 /pmc/articles/PMC7080809/ /pubmed/32188916 http://dx.doi.org/10.1038/s41598-020-61821-6 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Miyazaki, Teruo
Sasaki, Sei-Ich
Toyoda, Atsushi
Wei, Fan-Yan
Shirai, Mutsumi
Morishita, Yukio
Ikegami, Tadashi
Tomizawa, Kazuhito
Honda, Akira
Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats
title Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats
title_full Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats
title_fullStr Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats
title_full_unstemmed Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats
title_short Impaired bile acid metabolism with defectives of mitochondrial-tRNA taurine modification and bile acid taurine conjugation in the taurine depleted cats
title_sort impaired bile acid metabolism with defectives of mitochondrial-trna taurine modification and bile acid taurine conjugation in the taurine depleted cats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080809/
https://www.ncbi.nlm.nih.gov/pubmed/32188916
http://dx.doi.org/10.1038/s41598-020-61821-6
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