Key result
Nebivolol treatment (10 mg/kg once or twice daily) significantly attenuated pulmonary arterial pressure and reduced right ventricular hypertrophy in rats with monocrotaline-induced pulmonary hypertension.
Why the study?
Does nebivolol reduce pulmonary arterial pressure and right ventricular hypertrophy in rats with monocrotaline-induced pulmonary hypertension?
Does nebivolol reduce pulmonary arterial pressure and right ventricular hypertrophy in rats with monocrotaline-induced pulmonary hypertension?
In a rat model of monocrotaline-induced pulmonary hypertension, nebivolol attenuated pulmonary arterial pressure and right ventricular hypertrophy without causing systemic hypotension.
Supports preclinical evaluation of nebivolol in pulmonary hypertension; leaves open translation to human disease.
Pulmonary hypertension is a rare disorder that, without treatment, is progressive and fatal within 3-4 years. Current treatment involves a diverse group of drugs that target the pulmonary vascular bed. In addition, strategies that increase nitric oxide (NO) formation have a beneficial effect in rodents and patients. Nebivolol, a selective β1 adrenergic receptor-blocking agent reported to increase NO production and stimulate β3 receptors, has vasodilator properties suggesting that it may be beneficial in the treatment of pulmonary hypertension. The present study was undertaken to determine whether nebivolol has a beneficial effect in monocrotaline-induced (60 mg/kg) pulmonary hypertension in the rat. These results show that nebivolol treatment (10 mg/kg, once or twice daily) attenuates pulmonary hypertension, reduces right ventricular hypertrophy, and improves pulmonary artery remodeling in monocrotaline-induced pulmonary hypertension. This study demonstrates the presence of β3 adrenergic receptor immunoreactivity in pulmonary arteries and airways and that nebivolol has pulmonary vasodilator activity. Studies with β3 receptor agonists (mirabegron, BRL 37344) and antagonists suggest that β3 receptor-mediated decreases in systemic arterial pressure occur independent of NO release. Our results suggest that nebivolol, a selective vasodilating β1 receptor antagonist that stimulates β3 adrenergic receptors and induces vasodilation by increasing NO production, may be beneficial in treating pulmonary hypertensive disorders.
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Pankey et al. (2016) studied Monocrotaline-induced pulmonary hypertension. Nebivolol vs. Untreated monocrotaline-induced pulmonary hypertension rats was evaluated on Pulmonary arterial pressure and right ventricular hypertrophy (p=<0.05). Nebivolol treatment (10 mg/kg once or twice daily) significantly attenuated pulmonary arterial pressure and reduced right ventricular hypertrophy in rats with monocrotaline-induced pulmonary hypertension.
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