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PMID: 21097804 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Long-term effects of intrauterine growth restriction on cardiac metabolism and susceptibility to ischaemia/reperfusion.

Cardiovascular research ·Vol. 90 ·No. 2 ·2011-05-01 ·Pages 285-94

Rueda-Clausen CF, Morton JS, Lopaschuk GD, Davidge ST

Abstract

Adult offspring who are born intrauterine growth restricted (IUGR) are at risk of developing cardiovascular diseases during adulthood. Additionally, several cardiac diseases are associated with changes in myocardial energy metabolism. However, the potential long-term effects of being born IUGR on cardiac energetics are unknown. The aim of this study was to assess the long-term effect of IUGR on cardiac performance and energy metabolism under aerobic conditions and after ischaemia/reperfusion (IR) injury. To induce IUGR, pregnant Sprague-Dawley rats were randomly assigned to hypoxic (11.5% O(2)) or control (21% O(2)) environments from day 15 to 21 of pregnancy. Cardiac susceptibility to IR was evaluated in male and female offspring at 4 (young-adult) or 12 (ageing) months of age using isolated working hearts. Cardiac production of energy was evaluated using radiolabelled substrates. Both male and female IUGR offspring exhibited an increased susceptibility to IR injury compared with controls (P< 0.05) as well as an increased post-ischaemic production of protons (P< 0.001) secondary to a mismatch between myocardial glycolysis and glucose oxidation rates. Moreover, offspring born IUGR exhibited an increased myocardial production of acetyl-CoA during reperfusion. The mismatch between energy production and cardiac performance indicates that in IUGR offspring, cardiac efficiency during reperfusion was decreased relative to controls. Our results suggest that hypoxia-induced IUGR has long-term effects on cardiac susceptibility to IR injury that are independent of sex and age. Moreover, we identified a mismatch in glucose metabolism, leading to proton accumulation in the post-ischaemic myocardium of offspring born IUGR as a potential mechanism involved.

MeSH Terms
Age Factors Animals Disease Models, Animal Energy Metabolism/physiology Female Fetal Growth Retardation/metabolism,physiopathology Glycolysis/physiology Heart/embryology,physiology Hypoxia/metabolism,physiopathology Male Myocardial Reperfusion Injury/metabolism,physiopathology Myocardium/metabolism Oxygen/administration & dosage Pregnancy Prenatal Exposure Delayed Effects/metabolism,physiopathology Rats Rats, Sprague-Dawley
Chemicals
Oxygen
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rueda-Clausen Christian F
Department of Physiology, University of Alberta, Edmonton, Canada.
Morton Jude S
Lopaschuk Gary D
Davidge Sandra T
Article Info
Journal
Cardiovascular research
Abbr.
Cardiovasc Res
ISSN
1755-3245
Published
2011-05-01
Epub
2010-00-19
Pages
285-94
Language
English
Region
England
NLM ID
0077427
Subset
IM
Grants
Canadian Institutes of Health Research · Canada
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