Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Sutherland, Megan R., Béland, Chanel, Lukaszewski, Marie‐Amélie, Cloutier, Anik, Bertagnolli, Mariane, Nuyt, Anne Monique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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
_version_ 1782448075558617088
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
work_keys_str_mv AT sutherlandmeganr ageandsexrelatedchangesinratrenalfunctionandpathologyfollowingneonatalhyperoxiaexposure
AT belandchanel ageandsexrelatedchangesinratrenalfunctionandpathologyfollowingneonatalhyperoxiaexposure
AT lukaszewskimarieamelie ageandsexrelatedchangesinratrenalfunctionandpathologyfollowingneonatalhyperoxiaexposure
AT cloutieranik ageandsexrelatedchangesinratrenalfunctionandpathologyfollowingneonatalhyperoxiaexposure
AT bertagnollimariane ageandsexrelatedchangesinratrenalfunctionandpathologyfollowingneonatalhyperoxiaexposure
AT nuytannemonique ageandsexrelatedchangesinratrenalfunctionandpathologyfollowingneonatalhyperoxiaexposure