Intrauterine growth restriction combined with a maternal high‐fat diet increases hepatic cholesterol and low‐density lipoprotein receptor activity in rats

• Published in: Physiological reports 2016-07, Vol.4 (13), p.e12862-n/a
• Main Authors: Zinkhan, Erin K., Zalla, Jennifer M., Carpenter, Jeanette R., Yu, Baifeng, Yu, Xing, Chan, Gary, Joss‐Moore, Lisa, Lane, Robert H.
• Format: Article
• Language: English
• Subjects: Adults; Age Factors; Animal Nutritional Physiological Phenomena; Animals; Carbohydrates; Cesarean section; Cholesterol; Cholesterol - metabolism; Diet; Diet, High-Fat; Disease Models, Animal; Endocrine and Metabolic Conditons, Disorders and Treatments; Female; Females; Fetal Growth Retardation - metabolism; Fetal Growth Retardation - physiopathology; Fetuses; Gender differences; High fat diet; Hypercholesterolemia; Intrauterine exposure; intrauterine growth restriction; Lactation; Ldlr; Lipid metabolism; Lipoproteins; Liver; Liver - metabolism; Low density lipoprotein; Low density lipoprotein receptors; Male; Males; maternal high‐fat diet; Maternal Nutritional Physiological Phenomena; Maternal, Fetal and Neonatal Physiology; Metabolism; Morbidity; Nutrition; Offspring; Original Research; Physiology; Pregnancy; Prenatal Exposure Delayed Effects; Proteins; Rats, Sprague-Dawley; Receptor density; Receptors, LDL - metabolism; Regulatory Pathways; Reproductive Conditions, Disorders and Treatments; Rodents; Studies; Surgery; Up-Regulation
• ISSN: 2051-817X; 2051-817X
• DOI: 10.14814/phy2.12862

Intrauterine growth restriction (IUGR) and maternal consumption of a high‐saturated‐fat diet (HFD) increase the risk of hypercholesterolemia, a leading cause of morbidity and mortality. Many pregnant women eat a HFD, thus exposing the fetus to a HFD in utero. The cumulative effect of in utero exposure to IUGR and a HFD on offspring cholesterol levels remains unknown. Furthermore, little is known about the mechanism through which IUGR and maternal HFD consumption increase cholesterol. We hypothesize that IUGR combined with a maternal HFD would increase offspring serum and hepatic cholesterol accumulation via alteration in levels of key proteins involved in cholesterol metabolism. To test our hypothesis we used a rat model of surgically induced IUGR and fed the dams a regular diet or a HFD. HFD‐fed dams consumed the same kilocalories as regular diet‐fed dams, with no difference between surgical intervention groups. In the offspring, IUGR combined with a maternal HFD increased hepatic cholesterol levels, low‐density lipoprotein (LDL) receptor protein levels, and Ldlr activity in female rat offspring at birth and both sexes at postnatal day 14 relative to non‐IUGR offspring both from regular diet‐ and HFD‐fed dams. These findings suggest that IUGR combined with a maternal HFD increases hepatic cholesterol accumulation via increased LDL cholesterol uptake into the liver with resulting persistent increases in hepatic cholesterol accumulation. Two disparate perinatal insults, intrauterine growth restriction and maternal consumption of a high‐fat diet, frequently occur together and increase the risk of developing hyperlipidemia in the offspring. Our findings show that the combination of intrauterine growth restriction and a maternal high‐fat diet in rats increases offspring hepatic cholesterol, low‐density lipoprotein receptor protein levels, and low‐density lipoprotein receptor activity at birth and at postnatal day 14.