Developmental expression of rabbit cytochrome P450 CYP1 A1, CYP1 A2 and CYP3 A6 genes
- 1 April 1991
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 197 (1) , 145-153
- https://doi.org/10.1111/j.1432-1033.1991.tb15893.x
Abstract
Developmental expression of CYP1A1, CYP1A2 and CYP3A6 in the rabbit have been studied. Cytochromes P450IA1, P450IA2 and P450IIIA6 exhibited comparable patterns of developmental expression. Present at low level (less than 0.05 nmol/mg) in the new born animal up to week 3, these proteins sharply accumulated between weeks 3 and 4 to reach a maximum by week 4 (P450IA1, 0.2 nmol/mg; P450IA2, 0.8 nmol/mg; P450IIIA6, 0.12 nmol/mg) and decreased in the adult (P450IA1, 0.2 nmol/mg; P450IA2, 0.4 nmol/mg; P450IIIA6, 0.09 nmol/mg). Cytochromes P450IA1 and P450IA2 were not expressed in the untreated fetus. Onset of CYP3A6 gene expression occurred at day 30 of gestation and both transcription and mRNA accumulation were transplacentally inducible by rifampicin only shortly before birth, i.e. after treatment of the females between days 28 and 30 of gestation. Both long (1.85 kb) and short (1.7 kb) mRNA transcripts were expressed in untreated or rifampicin-treated fetuses. CYP3A6 gene expression was also induced by rifampicin in 1-week-old and 2-week-old animals. Developmental expression of CYP1A1 and CYP1A2 genes was shown to be closely related to the diet change accompanying weaning which occurs at weeks 3-4. In animals subjected to either delayed (week 6) or early (week 2) weaning, sharp accumulation of messages, proteins and related activities were delayed or anticipated accordingly with respect to normal weaning. Artificially scheduled weaning gave similar results when repeated with biological-grade lucern (grown in the absence of chemical fertilizers, pesticides, etc.), the main constituent of commercial rabbit chow. While CYP3A6 gene expression could be brought forward by early weaning at week 2, both message and protein did not exhibit increased accumulation after delayed weaning at week 6, and remained at the low level of the new born animal. Treatment of 1-week-old and 2-week-old animals with triiodothyronine or of 3-week-old animals with propylthiouracil, an antithyroid factor, did not modify the normal pattern of developmental expression of genes CYP1A1, CYP1A2 and CYP3A6. It is concluded that (a) the onset of CYP3A6 gene expression in the fetus occurs at day 30 of gestation, (b) expression of this gene may be induced transplacentally by rifampicin, (c) CYP1A1, CYP1A2 and CYP3A6 gene expression is sharply activated at weaning, and (d) thyroid hormones appear not to be responsible for the pattern of developmental expression of these genes in the rabbit.Keywords
This publication has 52 references indexed in Scilit:
- Fetus-specific expression of a form of cytochrome P-450 in human liversBiochemistry, 1990
- Ontogenesis of rabbit liver cytochrome P450European Journal of Biochemistry, 1990
- Occurrence and inducibility of cytochrome P 450IIIA in maternal and fetal rats during prenatal developmentBiochemistry, 1989
- Thyroid hormone suppression of hepatic levels of phenobarbital-inducible P-450b AND P-450e and other neonatal P-450S in hypophysectomized ratsBiochemical and Biophysical Research Communications, 1989
- Age-related changes in the expression of cytochrome P-450 (b+e) gene in the rat after phenobarbitone administrationBiochemical and Biophysical Research Communications, 1988
- Effects of growth hormone on cytochrome P-450jBiochemical and Biophysical Research Communications, 1988
- Ontogenic Development of 7‐Ethoxycoumarin and 7‐Ethoxyresorufii 0‐Deethylase in the Rat and Effect of Monoclonal AntibodiesBasic & Clinical Pharmacology & Toxicology, 1988
- Transplacental Pharmacokinetics of the Antituberculosis DrugsClinical Pharmacokinetics, 1987
- Foetal and neonatal development of cytochrome P-450 and cytochrome P-448 catalysed mixed function oxidases in the rat: Induction by 3-methylcholanthreneToxicology, 1985
- Stimulation of 3T3 cells induces transcription of the c-fos proto-oncogeneNature, 1984