Tual L, Morel O-E, Favret F, Fouillit M, Guernier C, Buvry A, Germain L, Dhonneur G, Bernaudin J-F, Richalet J-P
Université Paris 13, Laboratoire , Résponses cellulaires et fonctionnelles à l'hypoxie, EA 2363, Association pour la Recherche en Physiologie de l'Environment, 74 rue Marcen Cachin, 93017, Bobigny, France.
Pflugers Arch. 2006 Jul;452(4):371-9. doi: 10.1007/s00424-006-0058-5. Epub 2006 Apr 26.
Right ventricular hypertrophy induced by chronic hypoxia is mainly due to a mechanical stress upon the ventricular wall secondary to pulmonary arterial hypertension. However, the hypoxic chronic activation of the sympathetic nervous system can contribute to the development of right ventricular hypertrophy either via myocardial adrenergic receptors and/or a vasoconstriction and remodeling of pulmonary arteries. To highlight the specific role of the sympathetic nervous system on hypoxia-induced right ventricular hypertrophy and particularly the efficiency of carvedilol, our study compared physiological, myocardial, and pulmonary arterial morphometric data in rats treated by alpha-(prazosin), or beta-(propranolol) or alphabeta-(carvedilol) antagonist and exposed to chronic hypobaric hypoxia (2 weeks at 380 mmHg barometric pressure). In chronic hypoxia, both systolic right ventricular pressure and Fulton's ratio (right/(left+septum) ventricular weight) were lower in rats treated by prazosin (-16.7 and -13.6%), propranolol (-28.6 and -12.7%) and carvedilol (-15.9 and -14.3%) respectively when compared to glucose (p<0.05). Surprisingly, prazosin was unable to reduce right ventricular hypertrophy induced by chronic hypoxia, whereas, left ventricular weight increased. Wall thickness index of pulmonary arteries increased in chronic hypoxia and was reduced by carvedilol. In conclusion, the hypoxia-induced activation of the adrenergic system participates in the development of right ventricular hypertrophy. Carvedilol is effective in reducing hypoxia-induced right ventricular hypertrophy, pulmonary arterial hypertension, and muscularization of pulmonary arteries.
慢性缺氧诱导的右心室肥厚主要是由于肺动脉高压继发于心室壁的机械应力。然而,交感神经系统的慢性缺氧激活可通过心肌肾上腺素能受体和/或肺动脉的血管收缩及重塑促进右心室肥厚的发展。为突出交感神经系统在缺氧诱导的右心室肥厚中的特定作用,特别是卡维地洛的疗效,我们的研究比较了用α-(哌唑嗪)、β-(普萘洛尔)或αβ-(卡维地洛)拮抗剂治疗并暴露于慢性低压缺氧(在380 mmHg气压下2周)的大鼠的生理、心肌和肺动脉形态学数据。在慢性缺氧状态下,与给予葡萄糖的大鼠相比,给予哌唑嗪(-16.7%和-13.6%)、普萘洛尔(-28.6%和-12.7%)和卡维地洛(-15.9%和-14.3%)的大鼠的右心室收缩压和富尔顿比值(右心室重量/(左心室重量+室间隔重量))均降低(p<0.05)。令人惊讶的是,哌唑嗪无法减轻慢性缺氧诱导的右心室肥厚,而左心室重量增加。慢性缺氧时肺动脉壁厚度指数增加,而卡维地洛可使其降低。总之,缺氧诱导的肾上腺素能系统激活参与了右心室肥厚的发展。卡维地洛可有效减轻缺氧诱导的右心室肥厚、肺动脉高压和肺动脉肌化。