| Literature DB >> 19823102 |
Ole Hartvig Mortensen1, Hanne Lodberg Olsen, Lis Frandsen, Peter Eigil Nielsen, Finn Cilius Nielsen, Niels Grunnet, Bjørn Quistorff.
Abstract
UNLABELLED: We examined gene expression changes in liver and skeletal muscle of newborn mice subjected to a maternal low protein (LP) or normal protein (NP) diet during pregnancy, with or without taurine supplementation in the drinking water. LP offspring had a 40% lower birthweight than NP offspring, whereas it was reduced by only 20% with taurine supplementation. Microarray gene expression analysis revealed significant changes in 2012 genes in liver and 967 genes in skeletal muscle of LP offspring. By unknown mechanisms, taurine partially or fully prevented 30 and 46% of these expression changes, respectively. Mitochondrial genes, in particular genes associated with oxidative phosphorylation, were more abundantly changed in LP offspring, with primarily up-regulation in liver but down-regulation in skeletal muscle. In both tissues, citrate synthase activity remained unchanged. Taurine preferentially rescued changes in genes concerned with fatty acid metabolism in liver and with oxidative phoshorylation and tri carboxylic acid (TCA) cycle in skeletal muscle. ABBREVIATIONS: Gestational protein restriction resulted in lower birthweight associated with significant gene expression changes, which was different in liver and muscle of offspring. However, a major part of the birthweight decrease and the expression changes were prevented by maternal taurine supplementation, implying taurine is a key component in metabolic fetal programming.Entities:
Mesh:
Substances:
Year: 2010 PMID: 19823102 DOI: 10.1203/PDR.0b013e3181c4735c
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756