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Fetal Physiological Programming
1Endocrinology and Metabolism Unit, Developmental Origins of Health and Disease (DOHaD) Division, School of Medicine, University of Southampton, Southampton General Hospital, and 2Centre for DOHaD, University of Southampton, Princess Anne Hospital, Southampton; and 3Department of Clinical Biochemistry, University of Cambridge, Addenbrookes Hospital, Cambridge, United Kingdom
Submitted 26 May 2004 ; accepted in final form 7 September 2004
Maternal dietary Fe restriction reduced fasting plasma cholesterol and triglyceride (TG) concentrations in the fetuses, as well as decreased plasma TG levels in the adult offspring. To investigate how maternal Fe restriction was affecting fetal lipid metabolism, we investigated whether there were changes in liver lipid metabolism in the full-term fetuses. There was a
27% (P < 0.05) increase in cholesterol but
29% reduction (P = 0.01) in TG concentrations in the liver of the Fe-restricted fetuses. Hepatic mRNA levels of cholesterol 7
hydroxylase and liver X receptor-
(LXR
) were reduced by
50% (P < 0.01) and
34% (P < 0.01), respectively. As LXR
regulates expression of sterol response element binding protein-1c (SREBP-1c) expression, we measured SREBP-1c expression. There was an
43% (P < 0.001) reduction in mRNA levels of SREBP-1c and its response genes, including acetyl-CoA carboxylase by
35% (P = 0.01), fatty acid synthase by
18% (P = 0.05), and diacylglycerol acyltransferase by
19% (P = 0.03). Furthermore, protein levels of CD36 were reduced by
27% (P = 0.02) in Fe-restricted fetuses. In conclusion, changes in liver cholesterol and TG concentrations in Fe-restricted fetuses may be coordinated through reduced expression of heme-containing cholesterol 7
hydroxylase and its regulator LXR
, mainly via downregulation of expression of genes in bile acid synthesis and fatty acid synthesis pathways.
cholesterol; cholesterol 7 alpha hydroxylase; liver X receptor-alpha; fetus
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