Objective-To determine the effect of maternal hypercholesterolemia on hepatic cholesterol metabolism in the offspring in a mouse model. Study Design-Male and female wild type and apoE −/−KO (knockout for the apoprotein E [apoE]) gene) mice were crossbred to obtain all four possible genetic offspring types. The litters were maintained on regular chow and sacrificed at eight months of age. Liver samples were collected and the mRNA expression levels for SCAP, SREBP-1a, SREBP-2, HMGCR and LDLR determined using real-time RT-PCR.Results-We found a significant activation of the transcriptional activity of genes involved in endogenous cholesterol synthesis, as well as LDLR, in the liver of adult mice born to hypercholesterolemic dams.Conclusions-Reprogramming of hepatic cholesterol homeostasis may be the basis for an increased predisposition to hypercholesterolemia and atherosclerosis found in offspring of mice exposed to a high cholesterol environment during early life.
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