Elliott H L, McLean K, Meredith P A, Sumner D J, Reid J L
Br J Clin Pharmacol. 1984 May;17(5):565-72. doi: 10.1111/j.1365-2125.1984.tb02391.x.
Medroxalol, a new drug which has been reported to possess both alpha- and beta-adrenoceptor antagonist properties, was compared with labetalol in single dose studies in normotensive males. Oral doses of 400 mg of each drug significantly reduced blood pressure, both supine and erect, without significant changes in heart rate. The chronotropic and diastolic depressor responses to isoprenaline were significantly antagonised by both drugs, for at least 6-8 h after drug administration. Medroxalol was associated with significantly greater beta-adrenoceptor antagonism than labetalol. There was no significant antagonism by either drug of the pressor response to noradrenaline. However, in a sub-group of subjects the responses to the selective alpha 1-adrenoceptor agonist, phenylephrine, were consistent with modest alpha 1-adrenoceptor antagonism. This was significant only for labetalol. The ratios of beta 1- to alpha 1-adrenoceptor antagonism as calculated from the relative shifts of the isoprenaline and phenylephrine dose-response curves, were 3 to 1 for labetalol and about 7 to 1 for medroxalol.
美多心安,一种据报道具有α和β肾上腺素能受体拮抗特性的新药,在正常血压男性的单剂量研究中与拉贝洛尔进行了比较。口服400毫克每种药物均能显著降低仰卧位和直立位血压,心率无显著变化。给药后至少6 - 8小时,两种药物均能显著拮抗异丙肾上腺素引起的变时性和舒张期降压反应。美多心安比拉贝洛尔具有显著更强的β肾上腺素能受体拮抗作用。两种药物对去甲肾上腺素的升压反应均无显著拮抗作用。然而,在一组受试者中,对选择性α1肾上腺素能受体激动剂去氧肾上腺素的反应表明有适度的α1肾上腺素能受体拮抗作用。这仅对拉贝洛尔有显著意义。根据异丙肾上腺素和去氧肾上腺素剂量反应曲线的相对偏移计算得出的β1与α1肾上腺素能受体拮抗作用的比率,拉贝洛尔为3比1,美多心安约为7比1。