Ochi S, Nakazawa M, Kimura T, Nakagawa Y, Imai S
Department of Pharmacology, Niigata University School of Medicine, Japan.
Eur J Pharmacol. 1991 Feb 26;194(1):1-5. doi: 10.1016/0014-2999(91)90115-7.
The beta-antagonistic effects of celiprolol were assessed in isolated guinea-pig preparations. The pA2 values obtained were 7.84 +/- 0.07, 7.79 +/- 0.06 and 6.45 +/- 0.11 against the positive chronotropic and inotropic effects in the atria and relaxant effects in the trachea induced by isoproterenol, respectively, indicating that celiprolol is a cardioselective beta-antagonist. Celiprolol produced slight positive chronotropic and inotropic effects in atrial preparations and a uniquely strong relaxant effect in tracheal preparations. All these effects were attenuated by pretreatment with 10(-6) M atenolol or 10(-6) M propranolol. In pithed rats, celiprolol produced pressor responses at doses lower than 0.03 mg/kg and hypotensive responses at doses higher than 0.3 mg/kg. It produced sustained increases in heart rate in all doses applied. These effects were attenuated by pretreatment with 1 mg/kg of propranolol. The pressor response might be taken to be a reflection of an increase in cardiac function mediated by cardiac beta 1-receptor stimulation, while the hypotension may be ascribed mainly to stimulation of beta 2-adrenoceptors in the vascular system. It is concluded that celiprolol exerts a uniquely strong partial agonist activity at beta 2-adrenoceptors.
在离体豚鼠标本上评估了塞利洛尔的β受体拮抗作用。针对异丙肾上腺素引起的心房正性变时和变力作用以及气管舒张作用,所获得的pA2值分别为7.84±0.07、7.79±0.06和6.45±0.11,表明塞利洛尔是一种心脏选择性β受体拮抗剂。塞利洛尔在心房标本中产生轻微的正性变时和变力作用,在气管标本中产生独特的强效舒张作用。所有这些作用都可被10⁻⁶ M阿替洛尔或10⁻⁶ M普萘洛尔预处理所减弱。在脊髓麻醉大鼠中,塞利洛尔在低于0.03 mg/kg的剂量下产生升压反应,在高于0.3 mg/kg的剂量下产生降压反应。在所应用的所有剂量下,它都会使心率持续增加。这些作用可被1 mg/kg普萘洛尔预处理所减弱。升压反应可能被认为是心脏β1受体刺激介导的心脏功能增强的反映,而低血压可能主要归因于血管系统中β2肾上腺素能受体的刺激。结论是,塞利洛尔在β2肾上腺素能受体上具有独特的强效部分激动剂活性。