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Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice
Alterations in sulfur amino acid metabolism are associated with an increased risk of a number of common late-life diseases, which raises the possibility that metabolism of sulfur amino acids may change with age. The present study was conducted to understand the age-related changes in hepatic metabol...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Applied Pharmacology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839495/ https://www.ncbi.nlm.nih.gov/pubmed/28605831 http://dx.doi.org/10.4062/biomolther.2017.054 |
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author | Jeon, Jang Su Oh, Jeong-Ja Kwak, Hui Chan Yun, Hwi-yeol Kim, Hyoung Chin Kim, Young-Mi Oh, Soo Jin Kim, Sang Kyum |
author_facet | Jeon, Jang Su Oh, Jeong-Ja Kwak, Hui Chan Yun, Hwi-yeol Kim, Hyoung Chin Kim, Young-Mi Oh, Soo Jin Kim, Sang Kyum |
author_sort | Jeon, Jang Su |
collection | PubMed |
description | Alterations in sulfur amino acid metabolism are associated with an increased risk of a number of common late-life diseases, which raises the possibility that metabolism of sulfur amino acids may change with age. The present study was conducted to understand the age-related changes in hepatic metabolism of sulfur amino acids in 2-, 6-, 18- and 30-month-old male C57BL/6 mice. For this purpose, metabolite profiling of sulfur amino acids from methionine to taurine or glutathione (GSH) was performed. The levels of sulfur amino acids and their metabolites were not significantly different among 2-, 6- and 18-month-old mice, except for plasma GSH and hepatic homocysteine. Plasma total GSH and hepatic total homocysteine levels were significantly higher in 2-month-old mice than those in the other age groups. In contrast, 30-month-old mice exhibited increased hepatic methionine and cysteine, compared with all other groups, but decreased hepatic S-adenosylmethionine (SAM), S-adenosylhomocysteine and homocysteine, relative to 2-month-old mice. No differences in hepatic reduced GSH, GSH disulfide, or taurine were observed. The hepatic changes in homocysteine and cysteine may be attributed to upregulation of cystathionine β-synthase and down-regulation of γ-glutamylcysteine ligase in the aged mice. The elevation of hepatic cysteine levels may be involved in the maintenance of hepatic GSH levels. The opposite changes of methionine and SAM suggest that the regulatory role of SAM in hepatic sulfur amino acid metabolism may be impaired in 30-month-old mice. |
format | Online Article Text |
id | pubmed-5839495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-58394952018-03-07 Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice Jeon, Jang Su Oh, Jeong-Ja Kwak, Hui Chan Yun, Hwi-yeol Kim, Hyoung Chin Kim, Young-Mi Oh, Soo Jin Kim, Sang Kyum Biomol Ther (Seoul) Original Article Alterations in sulfur amino acid metabolism are associated with an increased risk of a number of common late-life diseases, which raises the possibility that metabolism of sulfur amino acids may change with age. The present study was conducted to understand the age-related changes in hepatic metabolism of sulfur amino acids in 2-, 6-, 18- and 30-month-old male C57BL/6 mice. For this purpose, metabolite profiling of sulfur amino acids from methionine to taurine or glutathione (GSH) was performed. The levels of sulfur amino acids and their metabolites were not significantly different among 2-, 6- and 18-month-old mice, except for plasma GSH and hepatic homocysteine. Plasma total GSH and hepatic total homocysteine levels were significantly higher in 2-month-old mice than those in the other age groups. In contrast, 30-month-old mice exhibited increased hepatic methionine and cysteine, compared with all other groups, but decreased hepatic S-adenosylmethionine (SAM), S-adenosylhomocysteine and homocysteine, relative to 2-month-old mice. No differences in hepatic reduced GSH, GSH disulfide, or taurine were observed. The hepatic changes in homocysteine and cysteine may be attributed to upregulation of cystathionine β-synthase and down-regulation of γ-glutamylcysteine ligase in the aged mice. The elevation of hepatic cysteine levels may be involved in the maintenance of hepatic GSH levels. The opposite changes of methionine and SAM suggest that the regulatory role of SAM in hepatic sulfur amino acid metabolism may be impaired in 30-month-old mice. The Korean Society of Applied Pharmacology 2018-03 2017-06-14 /pmc/articles/PMC5839495/ /pubmed/28605831 http://dx.doi.org/10.4062/biomolther.2017.054 Text en Copyright © 2018 The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jeon, Jang Su Oh, Jeong-Ja Kwak, Hui Chan Yun, Hwi-yeol Kim, Hyoung Chin Kim, Young-Mi Oh, Soo Jin Kim, Sang Kyum Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice |
title | Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice |
title_full | Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice |
title_fullStr | Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice |
title_full_unstemmed | Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice |
title_short | Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice |
title_sort | age-related changes in sulfur amino acid metabolism in male c57bl/6 mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839495/ https://www.ncbi.nlm.nih.gov/pubmed/28605831 http://dx.doi.org/10.4062/biomolther.2017.054 |
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