Sexual dimorphism in the fetal cardiac response to maternal nutrient restriction

Sribalasubashini Muralimanoharan, Cun Li, Ernesto S. Nakayasu, Cameron P. Casey, Thomas O. Metz, Peter W. Nathanielsz, Alina Maloyan

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Poor maternal nutrition causes intrauterine growth restriction (IUGR); however, its effects on fetal cardiac development are unclear. We have developed a baboon model of moderate maternal undernutrition, leading to IUGR. We hypothesized that the IUGR affects fetal cardiac structure and metabolism. Six control pregnant baboons ate ad-libitum (CTRL)) or 70% CTRL from 0.16 of gestation (G). Fetuses were euthanized at C-section at 0.9G under general anesthesia. Male but not female IUGR fetuses showed left ventricular fibrosis inversely correlated with birth weight. Expression of extracellular matrix protein TSP-1 was increased (p < 0.05) in male IUGR. Expression of cardiac fibrotic markers TGFβ, SMAD3 and ALK-1 were downregulated in male IUGRs with no difference in females. Autophagy was present in male IUGR evidenced by upregulation of ATG7 expression and lipidation LC3B. Global miRNA expression profiling revealed 56 annotated and novel cardiac miRNAs exclusively dysregulated in female IUGR, and 38 cardiac miRNAs were exclusively dysregulated in males (p < 0.05). Fifteen (CTRL) and 23 (IUGR) miRNAs, were differentially expressed between males and females (p < 0.05) suggesting sexual dimorphism, which can be at least partially explained by differential expression of upstream transcription factors (e.g. HNF4α, and NFκB p50). Lipidomics analysis of fetal cardiac tissue exhibited a net increase in diacylglycerol and plasmalogens and a decrease in triglycerides and phosphatidylcholines. In summary, IUGR resulting from decreased maternal nutrition is associated with sex-dependent dysregulations in cardiac structure, miRNA expression, and lipid metabolism. If these changes persist postnatally, they may program offspring for higher later life cardiac risk.

Original languageEnglish (US)
Pages (from-to)181-193
Number of pages13
JournalJournal of Molecular and Cellular Cardiology
Volume108
DOIs
StatePublished - Jul 1 2017

Fingerprint

Sex Characteristics
Mothers
Food
MicroRNAs
Growth
Fetus
Papio
Hepatocyte Nuclear Factor 4
Plasmalogens
Thrombospondin 1
Fetal Growth Retardation
Extracellular Matrix Proteins
Diglycerides
Autophagy
Fetal Development
Phosphatidylcholines
Lipid Metabolism
Birth Weight
Malnutrition
General Anesthesia

Keywords

  • Autophagy
  • Cardiac fibrosis
  • Lipidomics
  • Maternal undernutrition
  • miRNA
  • Sexual dimorphism

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

Cite this

Sexual dimorphism in the fetal cardiac response to maternal nutrient restriction. / Muralimanoharan, Sribalasubashini; Li, Cun; Nakayasu, Ernesto S.; Casey, Cameron P.; Metz, Thomas O.; Nathanielsz, Peter W.; Maloyan, Alina.

In: Journal of Molecular and Cellular Cardiology, Vol. 108, 01.07.2017, p. 181-193.

Research output: Contribution to journalArticle

Muralimanoharan, Sribalasubashini ; Li, Cun ; Nakayasu, Ernesto S. ; Casey, Cameron P. ; Metz, Thomas O. ; Nathanielsz, Peter W. ; Maloyan, Alina. / Sexual dimorphism in the fetal cardiac response to maternal nutrient restriction. In: Journal of Molecular and Cellular Cardiology. 2017 ; Vol. 108. pp. 181-193.
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