首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >Effects of the beta 2-adrenoceptor antagonist ICI 118551 on exercise tachycardia and isoprenaline-induced beta-adrenoceptor responses in man.
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Effects of the beta 2-adrenoceptor antagonist ICI 118551 on exercise tachycardia and isoprenaline-induced beta-adrenoceptor responses in man.

机译:β2肾上腺素受体拮抗剂ICI 118551对人运动性心动过速和异丙肾上腺素诱导的β肾上腺素受体反应的影响。

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摘要

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.
机译:ICI 118,551,口服5至80 mg,不会显着改变静息心率或血压。剂量低于40 mg时,运动性心动过速的减少速度低于10次/分钟。 ICI 118,551,10至40 mg,似乎没有降低异丙肾上腺素的收缩压的最大升高,但并未减弱舒张压,前臂血流和手指震颤的变化。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。在这些观察到的变化上,ICI 118,551 20 mg的作用类似于40 mg和普萘洛尔10 mg的作用,但大于阿替洛尔25 mg的作用。所有研究的ICI 118,551剂量均可减轻异丙肾上腺素的心动过速。在阿托品(0.04 mg / kg)之后,ICI 118,551 20 mg仍显着降低了异丙肾上腺素的作用,表明人心脏中可能存在功能性β2肾上腺素能受体。剂量小于40 mg时,ICI 118,551似乎是人体内β2肾上腺素受体的选择性竞争性拮抗剂。

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