Tung L H, Rand M J, Drummer O H, Louis W J
J Auton Pharmacol. 1982 Dec;2(4):217-33. doi: 10.1111/j.1474-8673.1982.tb00512.x.
1 Phenylephrine (1-100 microgram/kg, intravenously) produced dose-dependent increases in heart rate and blood pressure in the pithed rat. 2 The positive chronotropic response to phenylephrine (10 microgram/kg) was reduced in a dose-dependent manner by propranolol (0.01-0.3 mg/kg), but higher doses of propranolol (up to 3 mg/kg) did not reduce the response by more than about 50%. The residual response was virtually abolished by phentolamine (0.3 mg/kg) or prazosin (3 microgram/kg). Labetalol (3 mg/kg) which has both alpha- and beta-blocking activity, also abolished the positive chronotropic response. 3 The pressor response to phenylephrine (1-30 microgram/kg) was enhanced by propranolol (1 mg/kg) and abolished by phentolamine (1 mg/kg) and prazosin (30 microgram/kg). Labetalol (3 mg/kg) reduced the response to phenylephrine by 73%. 4 Propranolol (0.3 mg/kg) completely blocked the chronotropic and vasodepressor effects of isoprenaline (0.1 microgram/kg). 5 It is concluded that phenylephrine acts on both alpha 1- and beta 1-adrenoreceptors to produce an increase in heart rate, on alpha 1-adrenoreceptors to produce vasoconstriction and on beta 2-adrenoreceptors to produce vasodilation. This latter effect is usually masked by the predominant vasoconstrictor action.
1 去氧肾上腺素(1 - 100微克/千克,静脉注射)可使脊髓麻醉大鼠的心率和血压呈剂量依赖性增加。2 普萘洛尔(0.01 - 0.3毫克/千克)可使去氧肾上腺素(10微克/千克)引起的正性变时反应呈剂量依赖性降低,但更高剂量的普萘洛尔(高达3毫克/千克)降低反应的幅度不超过约50%。酚妥拉明(0.3毫克/千克)或哌唑嗪(3微克/千克)几乎完全消除了残余反应。具有α和β阻断活性的拉贝洛尔(3毫克/千克)也消除了正性变时反应。3 普萘洛尔(1毫克/千克)增强了对去氧肾上腺素(1 - 30微克/千克)的升压反应,而酚妥拉明(1毫克/千克)和哌唑嗪(30微克/千克)则消除了该反应。拉贝洛尔(3毫克/千克)使对去氧肾上腺素的反应降低了73%。4 普萘洛尔(0.3毫克/千克)完全阻断了异丙肾上腺素(0.1微克/千克)的变时和血管减压作用。5 得出的结论是,去氧肾上腺素作用于α1和β1肾上腺素能受体以增加心率,作用于α1肾上腺素能受体以产生血管收缩,作用于β2肾上腺素能受体以产生血管舒张。后一种作用通常被主要的血管收缩作用所掩盖。