Expression of liver carnitine palmitoyltransferase I and II genes during development in the rat - PubMed (original) (raw)
Expression of liver carnitine palmitoyltransferase I and II genes during development in the rat
S Thumelin et al. Biochem J. 1994.
Abstract
The enzyme activity and the expression (protein and mRNA concentrations) of genes encoding for hepatic carnitine palmitoyl-transferases (CPT) I and II were studied during neonatal development, in response to nutritional state at weaning and during the fed-starved transition in adult rats. The activity, the protein concentration and the level of mRNA encoding CPT I are low in foetal-rat liver and increase 5-fold during the first day of extra-uterine life. The activity and gene expression of CPT I are high during the entire suckling period, in the liver of 30-day-old rats weaned at 20 days on to a high-fat diet and in the liver of 48 h-starved adult rats. The activity and CPT I gene expression are markedly decreased in the liver of rats weaned on to a high-carbohydrate diet. By contrast, the activity, the protein concentration and the level of mRNA encoding CPT II are already high in the liver of term foetuses and remain at this level throughout the suckling period, irrespective of the nutritional state of the animals either at weaning or in the adult.
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References
- Biochem J. 1988 Jan 15;249(2):409-14 - PubMed
- J Biol Chem. 1993 Mar 15;268(8):5817-22 - PubMed
- Pediatr Res. 1988 Feb;23(2):224-8 - PubMed
- Nature. 1970 Aug 15;227(5259):680-5 - PubMed
- Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2160-4 - PubMed
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