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Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure
Preterm neonates are prematurely exposed to high oxygen levels at birth which may adversely impact ongoing renal development. The aim of this study was to determine the effects of neonatal hyperoxia exposure on renal function and morphology with aging. Sprague Dawley rat pups were raised in a hypero...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985552/ https://www.ncbi.nlm.nih.gov/pubmed/27528005 http://dx.doi.org/10.14814/phy2.12887 |
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author | Sutherland, Megan R. Béland, Chanel Lukaszewski, Marie‐Amélie Cloutier, Anik Bertagnolli, Mariane Nuyt, Anne Monique |
author_facet | Sutherland, Megan R. Béland, Chanel Lukaszewski, Marie‐Amélie Cloutier, Anik Bertagnolli, Mariane Nuyt, Anne Monique |
author_sort | Sutherland, Megan R. |
collection | PubMed |
description | Preterm neonates are prematurely exposed to high oxygen levels at birth which may adversely impact ongoing renal development. The aim of this study was to determine the effects of neonatal hyperoxia exposure on renal function and morphology with aging. Sprague Dawley rat pups were raised in a hyperoxic environment (80% oxygen) from P3 to P10 during ongoing postnatal nephrogenesis. Control litters were kept in room air (n = 6–8 litters/group; one male, one female/litter/age). Kidney function (urine and plasma creatinine, sodium, and protein) and morphology (renal corpuscle size, glomerulosclerosis, fibrosis, and glomerular crescents) were assessed at 1, 5, and 11 months of age. Neonatal hyperoxia exposure had no impact on body or kidney weights. Creatinine clearance was significantly reduced following hyperoxia exposure at 5 months; there was no significant effect on renal function at 1 or 11 months. The percentage of crescentic glomeruli (indicative of glomerular injury) was markedly increased in 11 month hyperoxia‐exposed males. Renal corpuscle size, glomerulosclerosis index, and renal fibrosis were not affected. Findings suggest that exposure to high oxygen levels during development may impact renal functional capacity and increase susceptibility to renal disease in adulthood depending on age and sex. |
format | Online Article Text |
id | pubmed-4985552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49855522016-08-22 Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure Sutherland, Megan R. Béland, Chanel Lukaszewski, Marie‐Amélie Cloutier, Anik Bertagnolli, Mariane Nuyt, Anne Monique Physiol Rep Original Research Preterm neonates are prematurely exposed to high oxygen levels at birth which may adversely impact ongoing renal development. The aim of this study was to determine the effects of neonatal hyperoxia exposure on renal function and morphology with aging. Sprague Dawley rat pups were raised in a hyperoxic environment (80% oxygen) from P3 to P10 during ongoing postnatal nephrogenesis. Control litters were kept in room air (n = 6–8 litters/group; one male, one female/litter/age). Kidney function (urine and plasma creatinine, sodium, and protein) and morphology (renal corpuscle size, glomerulosclerosis, fibrosis, and glomerular crescents) were assessed at 1, 5, and 11 months of age. Neonatal hyperoxia exposure had no impact on body or kidney weights. Creatinine clearance was significantly reduced following hyperoxia exposure at 5 months; there was no significant effect on renal function at 1 or 11 months. The percentage of crescentic glomeruli (indicative of glomerular injury) was markedly increased in 11 month hyperoxia‐exposed males. Renal corpuscle size, glomerulosclerosis index, and renal fibrosis were not affected. Findings suggest that exposure to high oxygen levels during development may impact renal functional capacity and increase susceptibility to renal disease in adulthood depending on age and sex. John Wiley and Sons Inc. 2016-08-15 /pmc/articles/PMC4985552/ /pubmed/27528005 http://dx.doi.org/10.14814/phy2.12887 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (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 Sutherland, Megan R. Béland, Chanel Lukaszewski, Marie‐Amélie Cloutier, Anik Bertagnolli, Mariane Nuyt, Anne Monique Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure |
title | Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure |
title_full | Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure |
title_fullStr | Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure |
title_full_unstemmed | Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure |
title_short | Age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure |
title_sort | age‐ and sex‐related changes in rat renal function and pathology following neonatal hyperoxia exposure |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985552/ https://www.ncbi.nlm.nih.gov/pubmed/27528005 http://dx.doi.org/10.14814/phy2.12887 |
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