Altered lung function at mid-adulthood in mice following neonatal exposure to hyperoxia.
- Publisher:
- ELSEVIER SCIENCE BV
- Publication Type:
- Journal Article
- Citation:
- Respiratory physiology & neurobiology, 2015, 218, pp. 21-27
- Issue Date:
- 2015-11
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Altered lung function at mid-adulthood in mice following neonatal exposure to hyperoxia.pdf | 386.33 kB |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Sozo, F | |
dc.contributor.author | Horvat, JC | |
dc.contributor.author | Essilfie, A-T | |
dc.contributor.author | O'Reilly, M | |
dc.contributor.author | Hansbro, PM | |
dc.contributor.author | Harding, R | |
dc.date.accessioned | 2021-03-03T05:14:56Z | |
dc.date.available | 2015-07-09 | |
dc.date.available | 2021-03-03T05:14:56Z | |
dc.date.issued | 2015-11 | |
dc.identifier.citation | Respiratory physiology & neurobiology, 2015, 218, pp. 21-27 | |
dc.identifier.issn | 1569-9048 | |
dc.identifier.issn | 1878-1519 | |
dc.identifier.uri | http://hdl.handle.net/10453/146710 | |
dc.description.abstract | Infants born very preterm are usually exposed to high oxygen concentrations but this may impair lung function in survivors in later life. However, the precise changes involved are poorly understood. We determined how neonatal hyperoxia alters lung function at mid-adulthood in mice. Neonatal C57BL/6J mice inhaled 65% oxygen (HE group) from birth for 7 days. They then breathed room air until 11 months of age (P11mo); these mice experienced growth restriction. Controls breathed only room air. To exclude the effects of growth restriction, a group of dams was rotated between hyperoxia and normoxia during the exposure period (HE+DR group). Lung function was measured at P11mo. HE mice had increased inspiratory capacity, work of breathing and tissue damping. HE+DR mice had further increases in inspiratory capacity and work of breathing, and reduced FEV100/FVC. Total lung capacity was increased in HE+DR males. HE males had elevated responses to methacholine. Neonatal hyperoxia alters lung function at mid-adulthood, especially in males. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | ELSEVIER SCIENCE BV | |
dc.relation.ispartof | Respiratory physiology & neurobiology | |
dc.relation.isbasedon | 10.1016/j.resp.2015.07.004 | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 1102 Cardiorespiratory Medicine and Haematology, 1109 Neurosciences, 1116 Medical Physiology | |
dc.subject.classification | Physiology | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Mice, Inbred C57BL | |
dc.subject.mesh | Animals, Newborn | |
dc.subject.mesh | Disease Models, Animal | |
dc.subject.mesh | Body Weight | |
dc.subject.mesh | Hyperoxia | |
dc.subject.mesh | Methacholine Chloride | |
dc.subject.mesh | Bronchoconstrictor Agents | |
dc.subject.mesh | Lung Volume Measurements | |
dc.subject.mesh | Sex Characteristics | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Animals, Newborn | |
dc.subject.mesh | Body Weight | |
dc.subject.mesh | Bronchoconstrictor Agents | |
dc.subject.mesh | Disease Models, Animal | |
dc.subject.mesh | Female | |
dc.subject.mesh | Hyperoxia | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Lung Volume Measurements | |
dc.subject.mesh | Male | |
dc.subject.mesh | Methacholine Chloride | |
dc.subject.mesh | Mice, Inbred C57BL | |
dc.subject.mesh | Sex Characteristics | |
dc.title | Altered lung function at mid-adulthood in mice following neonatal exposure to hyperoxia. | |
dc.type | Journal Article | |
utslib.citation.volume | 218 | |
utslib.location.activity | Netherlands | |
utslib.for | 1102 Cardiorespiratory Medicine and Haematology | |
utslib.for | 1109 Neurosciences | |
utslib.for | 1116 Medical Physiology | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
utslib.copyright.status | closed_access | * |
dc.date.updated | 2021-03-03T05:14:54Z | |
pubs.publication-status | Published | |
pubs.volume | 218 |
Abstract:
Infants born very preterm are usually exposed to high oxygen concentrations but this may impair lung function in survivors in later life. However, the precise changes involved are poorly understood. We determined how neonatal hyperoxia alters lung function at mid-adulthood in mice. Neonatal C57BL/6J mice inhaled 65% oxygen (HE group) from birth for 7 days. They then breathed room air until 11 months of age (P11mo); these mice experienced growth restriction. Controls breathed only room air. To exclude the effects of growth restriction, a group of dams was rotated between hyperoxia and normoxia during the exposure period (HE+DR group). Lung function was measured at P11mo. HE mice had increased inspiratory capacity, work of breathing and tissue damping. HE+DR mice had further increases in inspiratory capacity and work of breathing, and reduced FEV100/FVC. Total lung capacity was increased in HE+DR males. HE males had elevated responses to methacholine. Neonatal hyperoxia alters lung function at mid-adulthood, especially in males.
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