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β受体阻滞剂及内在拟交感活性对运动能力的影响。

Effect of beta blockade and intrinsic sympathomimetic activity on exercise performance.

作者信息

Ades P A, Brammell H L, Greenberg J H, Horwitz L D

出版信息

Am J Cardiol. 1984 Dec 1;54(10):1337-41. doi: 10.1016/s0002-9149(84)80093-4.

Abstract

Beta-adrenergic receptor blocking drugs with intrinsic sympathomimetic activity may have the advantage of not depressing myocardial function and pulse rate at rest. Little is known about their effects during exercise. Thus, the effects of small and large doses of pindolol, a nonselective beta-adrenergic blocking drug with intrinsic sympathomimetic activity, were compared with the effects of small and large doses of propranolol in 13 normal men during treadmill exercise. Compared with placebo, all drug regimens decreased exercise duration (p less than 0.001). There were no significant differences in duration between pindolol and propranolol, or between the small and large dose of each drug. Maximal oxygen consumption tended to be lower with all preparations compared with placebo (p less than 0.10). With smaller doses, decrements of maximal heart rate (HR) and HR-blood pressure (BP) product were equivalent for pindolol and propranolol (decreases of 46 vs 43 beats/min, and 13,000 vs 12,000 units). The HR-BP product decreased more with high-dose propranolol than high-dose pindolol (decrease of 18,000 vs 14,800 units) due to a greater decrement in HR with propranolol (decrease of 65 +/- 3 vs 53 +/- 3 beats/min). At both submaximal levels, for both low- and high-dose preparations, HR, BP and HR-BP product were lower for propranolol than for pindolol. Thus, in healthy subjects, pindolol and propranolol at doses that produced equivalent reductions in maximal oxygen consumption, exercise duration and, for the smaller dose, HR, had different effects on submaximal HR-BP product, an index of myocardial oxygen consumption, as a result of a higher HR and BP with pindolol.

摘要

具有内在拟交感活性的β-肾上腺素能受体阻断药物可能具有不抑制静息心肌功能和心率的优势。关于它们在运动期间的作用知之甚少。因此,在13名正常男性进行跑步机运动期间,比较了小剂量和大剂量吲哚洛尔(一种具有内在拟交感活性的非选择性β-肾上腺素能阻断药物)与小剂量和大剂量普萘洛尔的作用。与安慰剂相比,所有药物方案均缩短了运动持续时间(p<0.001)。吲哚洛尔和普萘洛尔之间,以及每种药物的小剂量和大剂量之间在持续时间上没有显著差异。与安慰剂相比,所有制剂的最大耗氧量均有降低趋势(p<0.10)。小剂量时,吲哚洛尔和普萘洛尔使最大心率(HR)和心率-血压(BP)乘积的降低幅度相当(分别降低46次/分钟和43次/分钟,以及13,000单位和12,000单位)。高剂量普萘洛尔使HR-BP乘积的降低幅度大于高剂量吲哚洛尔(分别降低18,000单位和14,800单位),这是因为普萘洛尔使HR的降低幅度更大(降低65±3次/分钟对53±3次/分钟)。在次最大运动水平时,无论是低剂量还是高剂量制剂,普萘洛尔组的HR、BP和HR-BP乘积均低于吲哚洛尔组。因此,在健康受试者中,吲哚洛尔和普萘洛尔在使最大耗氧量、运动持续时间以及小剂量时的HR产生同等程度降低的剂量下,对次最大HR-BP乘积(心肌耗氧量指标)产生了不同影响,这是由于吲哚洛尔使HR和BP更高所致。

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