Arnold J M, O'Connor P C, Riddell J G, Harron D W, Shanks R G, McDevitt D G
Br J Clin Pharmacol. 1985 May;19(5):619-30. doi: 10.1111/j.1365-2125.1985.tb02689.x.
ICI 118,551, 5 to 80 mg orally, did not significantly alter resting heart rate or blood pressure. In doses less than 40 mg the reduction in exercise tachycardia was under 10 beats/min. ICI 118,551, 10 to 40 mg, did not appear to reduce the maximum rise in systolic pressure with isoprenaline but did attenuate the changes in diastolic pressure, forearm blood flow and finger tremor. It also attenuated the isoprenaline-induced changes in serum glucose, insulin and potassium. On these observed changes, the effect of ICI 118,551 20 mg was similar to that of 40 mg and of propranolol 10 mg, but greater than that of atenolol 25 mg. An isoprenaline tachycardia was attenuated by all doses of ICI 118,551 studied. After atropine (0.04 mg/kg) ICI 118,551 20 mg still significantly reduced the effects of isoprenaline suggesting that functional beta 2-adrenoceptors may be present in the human heart. In doses less than 40 mg, ICI 118,551 appears to be a selective and competitive antagonist of beta 2-adrenoceptors in man.
ICI 118,551,口服5至80毫克,对静息心率或血压无显著影响。剂量低于40毫克时,运动性心动过速的降低幅度小于10次/分钟。10至40毫克的ICI 118,551似乎不会降低异丙肾上腺素引起的收缩压最大升高幅度,但会减弱舒张压、前臂血流量和手指震颤的变化。它还减弱了异丙肾上腺素引起的血清葡萄糖、胰岛素和钾的变化。基于这些观察到的变化,20毫克的ICI 118,551的效果与40毫克的ICI 118,551以及10毫克的普萘洛尔相似,但大于25毫克的阿替洛尔。所有研究剂量的ICI 118,551均能减弱异丙肾上腺素引起的心动过速。注射阿托品(0.04毫克/千克)后,20毫克的ICI 118,551仍能显著降低异丙肾上腺素的作用,这表明人类心脏中可能存在功能性β2 - 肾上腺素能受体。剂量低于40毫克时,ICI 118,551似乎是人体β2 - 肾上腺素能受体的选择性竞争性拮抗剂。