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Open AccessHighly AccessResearch article

Cardiac insulin-like growth factor-1 and cyclins gene expression in canine models of ischemic or overpacing cardiomyopathy

Maryam Mahmoudabady1,2 email, Myrielle Mathieu1 email, Karim Touihri1 email, Ielham Hadad1 email, Agnes Mendes Da Costa1 email, Robert Naeije1 email and Kathleen Mc Entee1 email

1Laboratory of Physiology, Faculty of Medicine, Université Libre de Bruxelles, Brussels, Belgium

2Department of Physiology, Faculty of Medicine, Mashhad University of Medical Sciences (MUMS), Mashhad, Iran

author email corresponding author email

BMC Cardiovascular Disorders 2009, 9:49doi:10.1186/1471-2261-9-49

Published: 9 October 2009

Abstract

Background

Insulin-like growth factor-1 (IGF-1), transforming growth factor β (TGFβ) and cyclins are thought to play a role in myocardial hypertrophic response to insults. We investigated these signaling pathways in canine models of ischemic or overpacing-induced cardiomyopathy.

Methods

Echocardiographic recordings and myocardial sampling for measurements of gene expressions of IGF-1, its receptor (IGF-1R), TGFβ and of cyclins A, B, D1, D2, D3 and E, were obtained in 8 dogs with a healed myocardial infarction, 8 dogs after 7 weeks of overpacing and in 7 healthy control dogs.

Results

Ischemic cardiomyopathy was characterized by moderate left ventricular systolic dysfunction and eccentric hypertrophy, with increased expressions of IGF-1, IGF-1R and cyclins B, D1, D3 and E. Tachycardiomyopathy was characterized by severe left ventricular systolic dysfunction and dilation with no identifiable hypertrophic response. In the latter model, only IGF-1 was overexpressed while IGF-1R, cyclins B, D1, D3 and E stayed unchanged as compared to controls. The expressions of TGFβ, cyclins A and D2 were comparable in the 3 groups. The expression of IGF-1R was correlated with the thickness of the interventricular septum, in systole and diastole, and to cyclins B, D1, D3 and E expression.

Conclusion

These results agree with the notion that IGF-1/IGF-1R and cyclins are involved in the hypertrophic response observed in cardiomyopathies.


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