The age-dependent development of abnormal cardiac metabolism in the peroxisome proliferator-activated receptor α-knockout mouse

Michael Dodd, Lucy Ambrose, Vicky Ball, Kieran Clarke, Carolyn A. Carr, Damian J Tyler

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Background and aims
Peroxisome proliferator-activated receptor α (PPARα) is crucial for regulating cardiac β-oxidation in the heart, liver, and kidney. Ageing can induce cardiac metabolic alterations, but the role of PPARα has not been extensively characterised. The aim of this research was to investigate the role of PPARα in the aged heart.
Methods
Hyperpolarized [1-13C]pyruvate was used to evaluate in vivo cardiac carbohydrate metabolism in fed and fasted young (3 months) and old (20-22 months) PPARα knockout (KO) mice versus controls. Cine MRI assessed cardiac structural and functional changes. Cardiac tissue analysis included qRT-PCR and western blotting for Ppara, medium chain acyl-CoA dehydrenase (MCAD), uncoupling protein (UCP) 3, glucose transporter (GLUT) 4 and PDH kinase (PDK) 1,2, and 4 expression.
Results
PPARα-KO hearts from both young and old mice showed significantly reduced Ppara mRNA and a 58-59% decrease in MCAD protein levels compared to controls. Cardiac PDH flux was similar in young control and PPARα-KO mice but 96% higher in old PPARα-KO mice. Differences between genotypes were consistent in fed and fasted states, with reduced PDH flux when fasted. Increased PDH flux was accompanied by a 179% rise in myocardial GLUT4 protein. No differences in PDK 1, 2, or 4 protein levels were observed between fed groups, indicating the increased PDH flux in aged PPARα-KO mice was not due to changes in PDH phosphorylation.
Conclusions
Aged PPARα-KO mice demonstrated higher cardiac PDH flux compared to controls, facilitated by increased myocardial GLUT4 protein levels, leading to enhanced glucose uptake and glycolysis.
Original languageEnglish
Article number118599
Pages (from-to)(In-Press)
JournalAtherosclerosis
Volume(In-Press)
Early online date10 Sept 2024
DOIs
Publication statusE-pub ahead of print - 10 Sept 2024

Funder

This work was supported by the British Heart Foundation.

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