Iuzhakov S D, Dolgun O V, Dorodnikova E V, Aniukhovskiĭ E P, Baldenkov G N, Rozenshtraukh L V, Medvedev O S, Mashkovskiĭ M D
Eksp Klin Farmakol. 1994 May-Jun;57(3):30-3.
The beta- and alpha-adrenoceptor blocking activity, the specificity of its beta-adrenoceptor blocking action, partial agonistic and membrane-stabilizing properties, as well as antihypertensive, antiarrhythmic, and anti-ischemic effects were studied. Proxodolol was shown to be superior to labetalol in its beta-adrenoceptor blocking action and similar to it in its alpha-adrenoceptor blocking agent. The drug has no a partial agonistic activity and produces a moderate membrane-stabilizing action. Proxodolol proved to be effective in treating experimental hypertension and arrhythmias. It exhibits anti-ischemic activity.
研究了其β-和α-肾上腺素能受体阻断活性、β-肾上腺素能受体阻断作用的特异性、部分激动和膜稳定特性,以及降压、抗心律失常和抗缺血作用。结果表明,普索洛尔在β-肾上腺素能受体阻断作用方面优于拉贝洛尔,在α-肾上腺素能受体阻断作用方面与拉贝洛尔相似。该药物无部分激动活性,具有中等程度的膜稳定作用。普索洛尔被证明对治疗实验性高血压和心律失常有效。它具有抗缺血活性。