Oates H F
Arch Int Pharmacodyn Ther. 1979 Feb;237(2):282-7.
The relationship between the hypotensive and alpha-adrenoceptor blocking actions of prazosin was investigated in anaesthetized rats. Pressor responses to norepinephrine and angiotensin II were determined before and after intravenous administration of prazosin, 0.0005 to 0.7 mg/kg. The prazosin-induced reduction in mean arterial pressure was recorded immediately before measurement of 87 such pairs of pressor reponses. The percentage antagonism of norepinephrine-induced pressor responsivity, corrected where necessary for non-specific changes in pressor sensitivity, was used as an index of alpha-adrenoceptor blockade. Linear regression analysis of the data revealed that there was a highly significant correlation between the degree of alpha-adrenoceptor blockade afforded by prazosin and the hypotensive response to the drug. The findings extend those of previous studies in which alpha-blocking properties of prazosin were demonstrated using doses of the drug 10(2) to 10(4)-fold greater than those producing significant hypotensive effects. The present results show that prazosin exhibits alpha-adrenoceptor blocking properties at much lower doses, such that a close relationship exists between its alpha-blocking activity and its hypotensive effects.
在麻醉大鼠中研究了哌唑嗪的降压作用与α-肾上腺素能受体阻断作用之间的关系。在静脉注射0.0005至0.7mg/kg哌唑嗪之前和之后,测定对去甲肾上腺素和血管紧张素II的升压反应。在测量87对这样的升压反应之前,立即记录哌唑嗪引起的平均动脉压降低。去甲肾上腺素诱导的升压反应性的拮抗百分比(必要时对升压敏感性的非特异性变化进行校正)用作α-肾上腺素能受体阻断的指标。对数据的线性回归分析表明,哌唑嗪提供的α-肾上腺素能受体阻断程度与该药物的降压反应之间存在高度显著的相关性。这些发现扩展了先前研究的结果,在先前的研究中,使用比产生显著降压作用的剂量大10²至10⁴倍的哌唑嗪剂量来证明其α阻断特性。目前的结果表明,哌唑嗪在低得多的剂量下就表现出α-肾上腺素能受体阻断特性,因此其α阻断活性与其降压作用之间存在密切关系。