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Effects of selective beta 2-adrenoceptor blockade on serum potassium and exercise performance in normal men.

机译:选择性β2-肾上腺素受体阻滞剂对正常男性血清钾和运动能力的影响。

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摘要

1. The differential effects of beta-adrenoceptor subtypes on potassium fluxes and exercise capacity were compared in eight healthy young men using single oral doses of the selective beta 2-adrenoceptor antagonist ICI-118551, the selective beta 1-adrenoceptor antagonist atenolol or the non-selective beta-adrenoceptor antagonist propranolol. The study was randomized, double-blind and placebo controlled. 2. Potassium in the venous effluent from the exercising muscles increased progressively with increasing exercise intensity. This response was augmented by propranolol, whereas neither atenolol nor ICI-118551 modified the response. After exercise potassium concentration fell exponentially with no difference between the treatment regimens. 3. Cumulative work was significantly reduced by ICI-118551 (6.4%, P = 0.04) and by propranolol (12.4%, P less than 0.01), whereas the reduction with atenolol (5.6%) did not reach statistical significance. 4. Atenolol and propranolol reduced peak heart rate by 23% and 29%, and peak systolic blood pressure by 9% and 11% respectively during maximal exercise. ICI-118551 caused a non-significant reduction in heart rate during submaximal exercise, with a significant reduction at maximum exercise (6% reduction), whereas systolic blood pressure was not different from placebo. Diastolic blood pressures were similar across all treatment regimens. 5. Similar glucose concentrations were obtained at baseline and at exhaustion during all treatment regimens. Lactate concentrations were comparable for any given exercise intensity irrespective of treatment regimens. Propranolol reduced lactate concentrations from the exercising muscles at maximum exercise in proportion to the reduction of maximal exercise capacity. 6. The subjective perception of fatigue was not affected by either beta 1- or beta 2-adrenoceptor blockade.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.比较了八位健康年轻人使用单次口服选择性β2-肾上腺素受体拮抗剂ICI-118551,选择性β1-肾上腺素受体拮抗剂阿替洛尔或非口服β-肾上腺素受体亚型对钾通量和运动能力的不同影响。选择性β-肾上腺素受体拮抗剂普萘洛尔。该研究是随机,双盲和安慰剂对照的。 2.运动强度随着运动强度的增加而逐渐增加。普萘洛尔可增强这种反应,而阿替洛尔和ICI-118551均未改变反应。运动后钾浓度呈指数下降,两种治疗方案之间无差异。 3. ICI-118551(6.4%,P = 0.04)和普萘洛尔(12.4%,P小于0.01)显着减少了累积功,而阿替洛尔(5.6%)的减少却没有统计学意义。 4.在最大程度的运动中,阿替洛尔和普萘洛尔分别使最高心率降低23%和29%,并使收缩压峰值降低9%和11%。 ICI-118551导致次最大运动期间心率无明显下降,最大运动时心率显着下降(下降6%),而收缩压与安慰剂无差异。在所有治疗方案中,舒张压均相似。 5.在所有治疗方案中,基线和力竭时均获得相似的葡萄糖浓度。不管治疗方案如何,对于任何给定的运动强度,乳酸浓度都是可比的。在最大运动量下,普萘洛尔降低了运动肌肉中乳酸的浓度,与最大运动能力的降低成比例。 6.β1或β2肾上腺素受体阻滞剂对疲劳的主观感知没有影响。(摘要截断为250字)

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