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Am J Physiol Heart Circ Physiol (April 18, 2002). doi:10.1152/ajpheart.01088.2001
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Articles in PresS, published online ahead of print April 18, 2002
Am J Physiol Heart Circ Physiol, 10.1152/ajpheart.01088.2001
Submitted on December 11, 2001
Accepted on April 10, 2002

Cardiac Modulations of Angiotensin II Receptor Expression in Rats with Hypoxic Pulmonary Hypertension

Christophe Adamy1, Patricia Oliviero1, Saadia Eddahibi2, Lydie Rappaport1, Jane-Lise Samuel1, Emmanuel Teiger2, and Catherine Chassagne1*

1 U 127, INSERM, Paris, Paris, France
2 U 492, INSERM, Creteil, Val-de-Marne, France

* To whom correspondence should be addressed. E-mail: catherine.chassagne{at}inserm.lrb.ap-hop-paris.fr.

Right-ventricular myocardial hypertrophy during hypoxic pulmonary hypertension is associated with local renin-angiotensin-system activation. The expression of angiotensin II type 1 (AT1) and type 2 (AT2) receptors in this setting has never been investigated. We have therefore examined the chronic hypoxia pattern of AT1 and AT2 expression in the right and left cardiac ventricles, using in situ binding and RT-PCR assays. Hypoxia produced right but not left ventricular hypertrophy after 7, 14 and 21 days, respectively. Hypoxia for 2 days was associated in each ventricle with a simultaneous and transient increase (P < 0.05) in AT1 binding and AT1 mRNA levels, in the absence of any significant change in AT2 expression level. Only after 14 days of hypoxia, AT2 binding increased (P < 0.05) in the two ventricles, concomitantly with a right ventricular decrease (P < 0.05) in AT2 mRNA. Along these data, AT1 and AT2 binding remained unchanged in both the left and hypertrophied right ventricles from rats treated with monocrotaline for 30 days. These results indicate that chronic hypoxia induces modulations of AT1 and AT2 receptors in both cardiac ventricles probably through direct and indirect mechanisms, respectively, which modulations may participate in myogenic (at the level of smooth or striated myocytes) rather than in the growth response of heart to hypoxia.




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K. Rakusan, Z. Chvojkova, P. Oliviero, I. Ostadalova, F. Kolar, C. Chassagne, J.-L. Samuel, and B. Ostadal
ANG II type 1 receptor antagonist irbesartan inhibits coronary angiogenesis stimulated by chronic intermittent hypoxia in neonatal rats
Am J Physiol Heart Circ Physiol, March 1, 2007; 292(3): H1237 - H1244.
[Abstract] [Full Text] [PDF]




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