Erina E V, Panfilov V V, Prokopova T N, D'iakonova E G, Beliakova E V
Kardiologiia. 1984 Jul;24(7):52-6.
Thirty-eight patients with stage IIB essential hypertension have been studied to determine the therapeutic activity of prazosine (pratsiol, "Orion" company, Finland) and its influence on the parameters of the central and peripheral hemodynamics. It has been established that following the oral administration of the drug, a hypotensive effect develops in 90-120 min and lasts for about six h. After a three-week course of treatment, the arterial pressure in the majority of patients decreased due to a reduction in the total peripheral resistance and the tone of the resistant vessels (arterioles). Simultaneously, there was an increase in the heart rate, end diastolic and stroke volumes and in the cardiac output. In a smaller portion of patients, the arterial pressure decreased due to the predominant reduction in the venous tone; the elasticity of the veins increased sharply, the end diastolic stroke and minute volumes diminished. The heart rate and total peripheral resistance showed no statistically significant changes. It has been established that pratsiol acts as an arterial and venous vasodilator and that it is advisable to use the drug in combination with beta-blockers and diuretics.
对38例IIB期原发性高血压患者进行了研究,以确定哌唑嗪(普拉西奥,芬兰“奥立安”公司生产)的治疗活性及其对中心和外周血流动力学参数的影响。已确定,口服该药物后,90 - 120分钟出现降压作用,持续约6小时。经过为期三周的治疗疗程后,大多数患者的动脉血压因总外周阻力和阻力血管(小动脉)张力降低而下降。同时,心率、舒张末期容积、每搏量和心输出量增加。在一小部分患者中,动脉血压下降是由于静脉张力的显著降低;静脉弹性急剧增加,舒张末期每搏量和分钟容积减小。心率和总外周阻力无统计学显著变化。已确定普拉西奥具有动脉和静脉血管舒张作用,建议将该药物与β受体阻滞剂和利尿剂联合使用。