Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J mice

Abstract Background Sex‐specific mechanisms explaining the association between mothers with obesity and the development of obesity in children are poorly characterized. Permanent changes in fetal brain glucocorticoid receptor (GR) expression caused by exposure to overnutrition in utero may program a...

Full description

Bibliographic Details
Main Authors: Debra Kulhanek, Raghavendra B. Rao, Megan E. Paulsen
Format: Article
Language:English
Published: Wiley 2021-08-01
Series:Obesity Science & Practice
Subjects:
Online Access:https://doi.org/10.1002/osp4.506
id doaj-b219dfd7260245dcba9be3f0f323f166
record_format Article
spelling doaj-b219dfd7260245dcba9be3f0f323f1662021-08-07T03:03:17ZengWileyObesity Science & Practice2055-22382021-08-017446247210.1002/osp4.506Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J miceDebra Kulhanek0Raghavendra B. Rao1Megan E. Paulsen2Department of Pediatrics Division of Neonatology University of Minnesota Medical School Minneapolis Minnesota USADepartment of Pediatrics Division of Neonatology University of Minnesota Medical School Minneapolis Minnesota USADepartment of Pediatrics Division of Neonatology University of Minnesota Medical School Minneapolis Minnesota USAAbstract Background Sex‐specific mechanisms explaining the association between mothers with obesity and the development of obesity in children are poorly characterized. Permanent changes in fetal brain glucocorticoid receptor (GR) expression caused by exposure to overnutrition in utero may program aberrant energy homeostasis, thereby predisposing the offspring to obesity. This study explores sex differences in brain GR expression using an established mouse model of overnutrition during pregnancy. Methods Female C57Bl/6J mice were fed control (CON) or high‐fat–high‐sucrose (HFHS) diets. Dam cholesterol, insulin, and triglycerides were measured by colorimetric assays. Fetal corticosterone exposure was measured by placental Abca1, Hsd11β1, Hsd11β2, and brain Nr3c1 (GR); Pomc expression measured by RT‐qPCR. Results Female, but not male, HFHS fetuses had 46% decreased brain GR and twofold increased Pomc expression. There was decreased Abca1 and Hsd11β1 but not Hsd11β2 expression in HFHS placentas. Caloric and sucrose intake, but not fat intake, in dams inversely correlated with fetal GR expression in both sexes. Excess sucrose consumption by dams inversely correlated with female fetal GR and directly correlated with female fetal Pomc expression. Conclusions Excess sucrose consumption in pregnant dams caused lower GR and higher Pomc expression in the female fetal brain. Clinical investigation of excess sucrose intake during pregnancy and its subsequent effect on hypothalamic‐pituitary‐adrenal axis activity and appetite in offspring may lead to novel, sex‐specific obesity prevention strategies in the development of obesity in children.https://doi.org/10.1002/osp4.506brainfetal programmingglucocorticoidsnutrition
collection DOAJ
language English
format Article
sources DOAJ
author Debra Kulhanek
Raghavendra B. Rao
Megan E. Paulsen
spellingShingle Debra Kulhanek
Raghavendra B. Rao
Megan E. Paulsen
Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J mice
Obesity Science & Practice
brain
fetal programming
glucocorticoids
nutrition
author_facet Debra Kulhanek
Raghavendra B. Rao
Megan E. Paulsen
author_sort Debra Kulhanek
title Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J mice
title_short Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J mice
title_full Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J mice
title_fullStr Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J mice
title_full_unstemmed Excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male C57Bl/6J mice
title_sort excess sucrose intake during pregnancy programs fetal brain glucocorticoid receptor expression in female but not male c57bl/6j mice
publisher Wiley
series Obesity Science & Practice
issn 2055-2238
publishDate 2021-08-01
description Abstract Background Sex‐specific mechanisms explaining the association between mothers with obesity and the development of obesity in children are poorly characterized. Permanent changes in fetal brain glucocorticoid receptor (GR) expression caused by exposure to overnutrition in utero may program aberrant energy homeostasis, thereby predisposing the offspring to obesity. This study explores sex differences in brain GR expression using an established mouse model of overnutrition during pregnancy. Methods Female C57Bl/6J mice were fed control (CON) or high‐fat–high‐sucrose (HFHS) diets. Dam cholesterol, insulin, and triglycerides were measured by colorimetric assays. Fetal corticosterone exposure was measured by placental Abca1, Hsd11β1, Hsd11β2, and brain Nr3c1 (GR); Pomc expression measured by RT‐qPCR. Results Female, but not male, HFHS fetuses had 46% decreased brain GR and twofold increased Pomc expression. There was decreased Abca1 and Hsd11β1 but not Hsd11β2 expression in HFHS placentas. Caloric and sucrose intake, but not fat intake, in dams inversely correlated with fetal GR expression in both sexes. Excess sucrose consumption by dams inversely correlated with female fetal GR and directly correlated with female fetal Pomc expression. Conclusions Excess sucrose consumption in pregnant dams caused lower GR and higher Pomc expression in the female fetal brain. Clinical investigation of excess sucrose intake during pregnancy and its subsequent effect on hypothalamic‐pituitary‐adrenal axis activity and appetite in offspring may lead to novel, sex‐specific obesity prevention strategies in the development of obesity in children.
topic brain
fetal programming
glucocorticoids
nutrition
url https://doi.org/10.1002/osp4.506
work_keys_str_mv AT debrakulhanek excesssucroseintakeduringpregnancyprogramsfetalbrainglucocorticoidreceptorexpressioninfemalebutnotmalec57bl6jmice
AT raghavendrabrao excesssucroseintakeduringpregnancyprogramsfetalbrainglucocorticoidreceptorexpressioninfemalebutnotmalec57bl6jmice
AT meganepaulsen excesssucroseintakeduringpregnancyprogramsfetalbrainglucocorticoidreceptorexpressioninfemalebutnotmalec57bl6jmice
_version_ 1721217192930836480