The effects of high doses of oxprenolol and of propranolol on pursuit rotor performance, reaction time and critical flicker frequency.

C W Ogle, P Turner, H Markomihelakis
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引用次数: 14

Abstract

The effects of oral oxprenolol (320 mg) or propranolol (240 or 320 mg) and of diazepam (5 mg) or lorazepam (2 mg) on pursuit rotor performance, reaction time and critical flicker frequency were investigated in healthy subjects in 3 separate studies. A 240-mg dose of propranolol significantly impaired pursuit rotor performance but not 320 mg of propranolol or oxprenolol. Both beta-adrenoceptor blockers did not affect reaction time or critical flicker frequency. Diazepam impaired pursuit rotor performance and reaction time, but not critical flicker frequency. Lorazepam generally impaired all three parameters. The findings suggest that it is possible for beta-adrenoceptor blockers to depress skeletal muscle activity without having a central effect, as shown by impairment of CNS function tests which rely also on muscle coordination but not of those relying only on central activity. These results also show that single oral doses of oxprenolol or propranolol, as high as 320 mg, do not have central effects, and support the belief that small anxiolytic doses of these blockers exert their actions through peripheral blockade of beta-adrenoceptors.

大剂量奥普萘洛尔和心得安对跟踪转子性能、反应时间和临界闪烁频率的影响。
在3个独立的研究中,研究了口服奥普萘洛尔(320 mg)或心得安(240或320 mg)以及地西泮(5 mg)或劳拉西泮(2 mg)对健康受试者的追踪转子性能、反应时间和临界闪烁频率的影响。240毫克的心得安显著损害了追踪转子的性能,而320毫克的心得安或奥普萘洛尔则没有。两种β -肾上腺素受体阻滞剂都不影响反应时间或临界闪烁频率。安定会影响追踪转子的性能和反应时间,但不会影响临界闪烁频率。劳拉西泮通常会损害这三个参数。研究结果表明,β -肾上腺素能受体阻滞剂有可能抑制骨骼肌活动而不产生中枢效应,正如中枢神经系统功能测试的损害所显示的那样,中枢神经系统功能测试也依赖于肌肉协调,而不依赖于中枢活动。这些结果还表明,单次口服剂量高达320毫克的奥普萘洛尔或心得安没有中枢效应,并支持小剂量抗焦虑阻滞剂通过外周阻断β -肾上腺素受体发挥作用的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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