Maternal hypercholesterolemia leads to activation of endogenous cholesterol synthesis in the offspring.

Abstract:

OBJECTIVE:The purpose of this study was 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 4 possible genetic offspring types. The litters were maintained on regular chow and sacrificed at 8 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. CONCLUSION: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.

journal_name

Am J Obstet Gynecol

authors

Goharkhay N,Tamayo EH,Yin H,Hankins GD,Saade GR,Longo M

doi

10.1016/j.ajog.2008.06.064

subject

Has Abstract

pub_date

2008-09-01 00:00:00

pages

273.e1-6

issue

3

eissn

0002-9378

issn

1097-6868

pii

S0002-9378(08)00696-0

journal_volume

199

pub_type

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