Ovcharov R, Mikhaĭlova S
Eksp Med Morfol. 1977;16(2):97-100.
The authors carried out a study on beta-adrenergic blockers Proprafnolol, Pindolol and Practolol, on an isolated uterus of a rat, obtained at various phases oestrus. The Beta-adrenergic blocker Pindolol manifested inhibiting effect on the spontaneous contractility of the uterus more marked after elevated level of gestagens. The pharmacological analysis gave foundation to the authors to assume that the relaxation of Pindolol was due to direct myotropic action. Propranolol in large doses and at high gestagenic level manifested antioxytocic activity. Practolol did not affect both spontaneous uterine activity as oxytoxin contraction.
作者对β-肾上腺素能阻滞剂普萘洛尔、吲哚洛尔和醋氨心安进行了一项研究,研究对象是处于发情周期不同阶段的大鼠离体子宫。β-肾上腺素能阻滞剂吲哚洛尔在孕激素水平升高后,对子宫的自发收缩表现出更明显的抑制作用。药理学分析使作者有理由认为,吲哚洛尔的松弛作用是由于直接的肌otropic作用。大剂量的普萘洛尔在高孕激素水平时表现出抗催产活性。醋氨心安对子宫的自发活动和催产素收缩均无影响。