scholarly journals Early Onset Intrauterine Growth Restriction in a Mouse Model of Gestational Hypercholesterolemia and Atherosclerosis

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Dolores Busso ◽  
Lilian Mascareño ◽  
Francisca Salas ◽  
Loni Berkowitz ◽  
Nicolás Santander ◽  
...  

The susceptibility to develop atherosclerosis is increased by intrauterine growth restriction and prenatal exposure to maternal hypercholesterolemia. Here, we studied whether mouse gestational hypercholesterolemia and atherosclerosis affected fetal development and growth at different stages of gestation. Female LDLR KO mice fed a proatherogenic, high cholesterol (HC) diet for 3 weeks before conception and during pregnancy exhibited a significant increase in non-HDL cholesterol and developed atherosclerosis. At embryonic days 12.5 (E12.5), E15.5, and E18.5, maternal gestational hypercholesterolemia and atherosclerosis were associated to a 22–24% reduction in male and female fetal weight without alterations in fetal number/litter or morphology nor placental weight or structure. Feeding the HC diet exclusively at the periconceptional period did not alter fetal growth, suggesting that maternal hypercholesterolemia affected fetal weight only after implantation. Vitamin E supplementation (1,000 UI of α-tocopherol/kg) of HC-fed females did not change the mean weight of E18.5 fetuses but reduced the percentage of fetuses exhibiting body weights below the 10th percentile of weight (HC: 90% vs. HC/VitE: 68%). In conclusion, our results showed that maternal gestational hypercholesterolemia and atherosclerosis in mice were associated to early onset fetal growth restriction and that dietary vitamin E supplementation had a beneficial impact on this condition.

2012 ◽  
Vol 32 (1-2) ◽  
pp. 116-122 ◽  
Author(s):  
Mónica Cruz-Lemini ◽  
Fàtima Crispi ◽  
Tim Van Mieghem ◽  
Daniel Pedraza ◽  
Rogelio Cruz-Martínez ◽  
...  

Author(s):  
P von Dadelszen ◽  
S Dwinnell ◽  
LA Magee ◽  
BC Carleton ◽  
A Gruslin ◽  
...  

2010 ◽  
Vol 36 (S1) ◽  
pp. 53-53
Author(s):  
M. C. Cruz Lemini ◽  
R. Cruz-Martinez ◽  
T. Van Mieghem ◽  
M. Parra-Cordero ◽  
J. Deprest ◽  
...  

2004 ◽  
Vol 190 (2) ◽  
pp. 296-304 ◽  
Author(s):  
Michal J Simchen ◽  
Fawaz Alkazaleh ◽  
S.Lee Adamson ◽  
Rory Windrim ◽  
Joyce Telford ◽  
...  

2012 ◽  
Vol 4 (2) ◽  
pp. 134-138 ◽  
Author(s):  
S. Mayeur ◽  
O. Cisse ◽  
A. Gabory ◽  
S. Barbaux ◽  
D. Vaiman ◽  
...  

Genetic variants in the FTO (fat mass- and obesity-associated) gene have the highest association of all obesity-associated genes. Its placental expression was shown to relate to birth weight, suggesting that it may participate in the control of fetal weight gain. To gain more insight into the implication of FTO in fetal growth, we measured its placental expression in samples including extremes of abnormal fetal growth, such as after intrauterine growth restriction (IUGR) or macrosomia in both rats and humans. In rats, fetal growth was modulated by maternal nutritional modifications. In humans, placental villi were collected from pathological pregnancies (i.e. with IUGR or fetal macrosomia). Placental FTO mRNA expression was reduced by IUGR but was not significantly affected by macrosomia in either rats or humans. Our data suggest that placental FTO may participate in interactions between the in utero environment and the control of fetal growth under IUGR conditions by modulating epigenetic processes.


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