Key result
Chronic hypoxia in rats transiently increased AT1 binding and mRNA at 2 days (P<0.05) and increased AT2 binding at 14 days (P<0.05) in both cardiac ventricles.
p-value: p=<0.05
Chronic hypoxia induces modulations of AT1 and AT2 receptors in both cardiac ventricles, which may participate in the myogenic response of the heart to hypoxia.
No clinical implications from rat hypoxia model; leaves open AT1/AT2 role in human ventricular adaptation.
Right ventricular myocardial hypertrophy during hypoxic pulmonary hypertension is associated with local renin-angiotensin system activation. The expression of angiotensin II type 1 (AT(1)) and type 2 (AT(2)) receptors in this setting has never been investigated. We have therefore examined the chronic hypoxia pattern of AT(1) and AT(2) 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 AT(1) binding and AT(1) mRNA levels in the absence of any significant change in AT(2) expression level. Only after 14 days of hypoxia, AT(2) binding increased (P < 0.05) in the two ventricles, concomitantly with a right ventricular decrease (P < 0.05) in AT(2) mRNA. Along these data, AT(1) and AT(2) 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 AT(1) and AT(2) 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 the heart to hypoxia.
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Adamy et al. (2002) studied Hypoxic pulmonary hypertension. Chronic hypoxia vs. Monocrotaline treatment / baseline was evaluated on AT1 and AT2 receptor expression in right and left cardiac ventricles (p=<0.05). Chronic hypoxia in rats transiently increased AT1 binding and mRNA at 2 days (P<0.05) and increased AT2 binding at 14 days (P<0.05) in both cardiac ventricles.
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