Rat lung antioxidant enzymes: differences in perinatal gene expression and regulation
- PMID: 1415724
- DOI: 10.1152/ajplung.1992.263.4.L466
Rat lung antioxidant enzymes: differences in perinatal gene expression and regulation
Abstract
The lung activity of the antioxidant enzymes (AOEs) copper, zinc superoxide dismutase (Cu,Zn SOD), catalase (CAT), and glutathione peroxidase (GP), but not manganese superoxide dismutase (Mn SOD), increases in rats during late gestation; the concentrations of Cu,Zn SOD mRNA and CAT mRNA also rise. During early postnatal exposure to > 95% O2, the lung activity of Cu,Zn SOD, CAT, and GP increases. We now show 1) the lung concentration of Mn SOD mRNA and GP mRNA does not increase in late gestation; 2) Mn SOD activity and the concentration of its mRNA and of GP mRNA increase during exposure of neonatal rats to > 95% O2; and 3) as previously shown for CAT mRNA, the increase in lung concentration of the mRNAs for Cu,Zn SOD, Mn SOD, and GP during early postnatal hyperoxia occurs with a 70-80% prolongation of the half-life of these mRNAs. We conclude that 1) in late gestation the level at which lung AOE gene expression is regulated differs among the enzymes, 2) the level at which lung AOE gene expression is regulated shortly after birth in response to > 95% O2 is uniform among the enzymes, and 3) the lung's AOE response to neonatal hyperoxia is not merely a step-up of its prenatal regulation but involves different regulatory mechanisms based on increased stability of AOE mRNAs.
Similar articles
-
Tolerance of rats to hyperoxia. Lung antioxidant enzyme gene expression.J Clin Invest. 1993 Feb;91(2):499-508. doi: 10.1172/JCI116228. J Clin Invest. 1993. PMID: 8432858 Free PMC article.
-
Differential gene expression of antioxidant enzymes in the perinatal rat lung.Pediatr Res. 1993 Jul;34(1):27-31. doi: 10.1203/00006450-199307000-00008. Pediatr Res. 1993. PMID: 8356014
-
Expression and developmental profile of antioxidant enzymes in human lung and liver.Am J Respir Cell Mol Biol. 1998 Dec;19(6):942-9. doi: 10.1165/ajrcmb.19.6.3248. Am J Respir Cell Mol Biol. 1998. PMID: 9843929
-
Possible mechanism for late gestational development of the antioxidant enzymes in the fetal rat lung.Biol Neonate. 1996;70(2):116-27. doi: 10.1159/000244356. Biol Neonate. 1996. PMID: 8864431 Review.
-
Genetic modulation of the cellular antioxidant defense capacity.Environ Health Perspect. 1990 Aug;88:77-82. doi: 10.1289/ehp.908877. Environ Health Perspect. 1990. PMID: 2272337 Free PMC article. Review.
Cited by
-
Epithelial ablation of Bcl-XL increases sensitivity to oxygen without disrupting lung development.Am J Respir Cell Mol Biol. 2010 Sep;43(3):376-85. doi: 10.1165/rcmb.2009-0165OC. Epub 2009 Oct 30. Am J Respir Cell Mol Biol. 2010. PMID: 19880821 Free PMC article.
-
Pertussis toxin treatment alters manganese superoxide dismutase activity in lung. Evidence for lung oxygen toxicity in air-breathing rats.J Clin Invest. 1994 Jun;93(6):2482-9. doi: 10.1172/JCI117257. J Clin Invest. 1994. PMID: 8200984 Free PMC article.
-
Transcription factor Klf4, induced in the lung by oxygen at birth, regulates perinatal fibroblast and myofibroblast differentiation.PLoS One. 2013;8(1):e54806. doi: 10.1371/journal.pone.0054806. Epub 2013 Jan 23. PLoS One. 2013. PMID: 23372771 Free PMC article.
-
Tolerance of rats to hyperoxia. Lung antioxidant enzyme gene expression.J Clin Invest. 1993 Feb;91(2):499-508. doi: 10.1172/JCI116228. J Clin Invest. 1993. PMID: 8432858 Free PMC article.
-
Effects of oxidative stress on expression of extracellular superoxide dismutase, CuZn-superoxide dismutase and Mn-superoxide dismutase in human dermal fibroblasts.Biochem J. 1994 Mar 1;298 ( Pt 2)(Pt 2):347-52. doi: 10.1042/bj2980347. Biochem J. 1994. PMID: 8135741 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous