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Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty
BACKGROUND: Post-puberty deterioration of kidneys is more rapid in males than in females. To reveal the underlying molecular mechanisms for this difference, we analyzed gender-dependent gene expression in kidneys of three groups of 36 day-old rats. RESULTS: The number of genes exhibiting gender-depe...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1934371/ https://www.ncbi.nlm.nih.gov/pubmed/17620128 http://dx.doi.org/10.1186/1471-2164-8-221 |
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author | Li, Li Boehn, Susanne N Yu, Xiaolei Zhang, Qingqin Kenzelmann, Marc Techel, Dieter Mohamed, Salah A Jakob, Petra Kraenzlin, Bettina Hoffmann, Sigrid Gretz, Norbert |
author_facet | Li, Li Boehn, Susanne N Yu, Xiaolei Zhang, Qingqin Kenzelmann, Marc Techel, Dieter Mohamed, Salah A Jakob, Petra Kraenzlin, Bettina Hoffmann, Sigrid Gretz, Norbert |
author_sort | Li, Li |
collection | PubMed |
description | BACKGROUND: Post-puberty deterioration of kidneys is more rapid in males than in females. To reveal the underlying molecular mechanisms for this difference, we analyzed gender-dependent gene expression in kidneys of three groups of 36 day-old rats. RESULTS: The number of genes exhibiting gender-dependent expression was highly influenced by the genetic background of the rat group examined. 373, 288 and 79 genes showed differential gene expression between males and females (p = 0.001) in US, Mhm and Mhm*BN rats, respectively. Of all gender dependently expressed genes, only 39 genes were differentially expressed in all tested groups and the direction of expression change was the same for those genes for all groups. The gene expression profile suggests higher metabolic and transport activities, enhanced cell proliferation, elevated oxidative stress, and altered vascular biology in males. Furthermore, elevated levels of superoxide anion (two- to three-fold) in males compared to females were detected at early puberty, but neither at pre-puberty nor at late puberty/early adulthood. CONCLUSION: Our data suggest that early puberty, with gender-related elevation in oxidative stress in males, is a key compromising factor on kidneys in males. |
format | Text |
id | pubmed-1934371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-19343712007-07-28 Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty Li, Li Boehn, Susanne N Yu, Xiaolei Zhang, Qingqin Kenzelmann, Marc Techel, Dieter Mohamed, Salah A Jakob, Petra Kraenzlin, Bettina Hoffmann, Sigrid Gretz, Norbert BMC Genomics Research Article BACKGROUND: Post-puberty deterioration of kidneys is more rapid in males than in females. To reveal the underlying molecular mechanisms for this difference, we analyzed gender-dependent gene expression in kidneys of three groups of 36 day-old rats. RESULTS: The number of genes exhibiting gender-dependent expression was highly influenced by the genetic background of the rat group examined. 373, 288 and 79 genes showed differential gene expression between males and females (p = 0.001) in US, Mhm and Mhm*BN rats, respectively. Of all gender dependently expressed genes, only 39 genes were differentially expressed in all tested groups and the direction of expression change was the same for those genes for all groups. The gene expression profile suggests higher metabolic and transport activities, enhanced cell proliferation, elevated oxidative stress, and altered vascular biology in males. Furthermore, elevated levels of superoxide anion (two- to three-fold) in males compared to females were detected at early puberty, but neither at pre-puberty nor at late puberty/early adulthood. CONCLUSION: Our data suggest that early puberty, with gender-related elevation in oxidative stress in males, is a key compromising factor on kidneys in males. BioMed Central 2007-07-09 /pmc/articles/PMC1934371/ /pubmed/17620128 http://dx.doi.org/10.1186/1471-2164-8-221 Text en Copyright © 2007 Li et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Li Boehn, Susanne N Yu, Xiaolei Zhang, Qingqin Kenzelmann, Marc Techel, Dieter Mohamed, Salah A Jakob, Petra Kraenzlin, Bettina Hoffmann, Sigrid Gretz, Norbert Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty |
title | Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty |
title_full | Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty |
title_fullStr | Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty |
title_full_unstemmed | Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty |
title_short | Faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty |
title_sort | faster rates of post-puberty kidney deterioration in males is correlated with elevated oxidative stress in males vs females at early puberty |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1934371/ https://www.ncbi.nlm.nih.gov/pubmed/17620128 http://dx.doi.org/10.1186/1471-2164-8-221 |
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