Hanada Kazuhiko, Asari Kazuhiko, Saito Masako, Kawana Jun-Ichi, Mita Mitsuo, Ogata Hiroyasu
Department of Biopharmaceutics, Meiji Pharmaceutical University, Tokyo, Japan.
Eur J Pharmacol. 2008 Jul 28;589(1-3):194-200. doi: 10.1016/j.ejphar.2008.04.055. Epub 2008 May 6.
A recent clinical study has shown that carvedilol has a significantly more favorable effect than metoprolol on survival rate in patients with heart failure. This may be due to actions of carvedilol such as beta(2)-adrenoceptor blockade, alpha-adrenergic receptor blockade and other properties such as anti-oxidant effects that are not yet fully understood. We compared the effects of racemic carvedilol, metoprolol and carvedilol enantiomers on cardiac hypertrophy at similar heart rate in rats with isoproterenol-induced cardiac hypertrophy. Continuous administration of isoproterenol for 2 weeks produced heart failure, which is characterized by an increased heart rate, cardiac hypertrophy and downregulation of beta-adrenoceptors. The doses of racemic carvedilol and metoprolol were adjusted to obtain a similar heart rate in rats with isoproterenol-induced cardiac hypertrophy. The reduction of left ventricular weight and improvement of cAMP production induced by carvedilol were superior to those induced by metoprolol. Although heart rate, blood pressure and cAMP production were not affected by R-carvedilol, left ventricular weight was significantly reduced as a result of alpha-adrenoceptor blockade. The improvement of cAMP production by S-carvedilol was significantly higher than that induced by coadministration of R-carvedilol and metoprolol, suggesting that beta(2)-adrenoceptor blockade partly contributed to the improvement of signal transduction in rats with isoproterenol-induced cardiac hypertrophy. This study has demonstrated that the effects of carvedilol on cAMP production and cardiac hypertrophy in rats with isoproterenol-induced cardiac hypertrophy are superior to those induced by metoprolol at a similar heart rate.
最近的一项临床研究表明,在心力衰竭患者中,卡维地洛对生存率的影响比美托洛尔显著更有利。这可能归因于卡维地洛的一些作用,如β₂-肾上腺素能受体阻滞、α-肾上腺素能受体阻滞以及其他尚未完全了解的特性,如抗氧化作用。我们在异丙肾上腺素诱导的心肌肥厚大鼠中,比较了消旋卡维地洛、美托洛尔和卡维地洛对映体在相似心率下对心肌肥厚的影响。连续给予异丙肾上腺素2周可导致心力衰竭,其特征为心率增加、心肌肥厚以及β-肾上腺素能受体下调。调整消旋卡维地洛和美托洛尔的剂量,以使异丙肾上腺素诱导的心肌肥厚大鼠获得相似的心率。卡维地洛诱导的左心室重量减轻和环磷酸腺苷(cAMP)生成改善优于美托洛尔。虽然R-卡维地洛不影响心率、血压和cAMP生成,但由于α-肾上腺素能受体阻滞,左心室重量显著减轻。S-卡维地洛对cAMP生成的改善显著高于R-卡维地洛与美托洛尔联合给药所诱导的改善,这表明β₂-肾上腺素能受体阻滞在一定程度上有助于异丙肾上腺素诱导的心肌肥厚大鼠信号转导的改善。本研究表明,在相似心率下,卡维地洛对异丙肾上腺素诱导的心肌肥厚大鼠cAMP生成和心肌肥厚的影响优于美托洛尔。