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首页> 外文期刊>European journal of applied physiology >Effects of beta2-adrenergic stimulation on exercise capacity in normal subjects.
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Effects of beta2-adrenergic stimulation on exercise capacity in normal subjects.

机译:β2-肾上腺素能刺激对正常受试者运动能力的影响。

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beta2-Adrenergic receptor agonists are believed to present with ergogenic properties. However, how combined respiratory, cardiovascular and muscular effects of these drugs might affect exercise capacity remain incompletely understood. The effects of salbutamol were investigated in 23 healthy subjects. The study was randomised, placebo-controlled in double-blind and followed a cross-over design. Salbutamol was given at the dose of 10 mug/min in 11 subjects and 20 mug/min iv in the other 12 subjects. Measurements included muscle sympathetic nerve activity (MSNA), ventilatory responses to hyperoxic hypercapnia (7% CO(2) in O(2,) central chemoreflex), isocapnic hypoxia (10% O(2) in N(2), peripheral chemoreflex) and isometric muscle contraction followed by a local circulatory arrest (metaboreflex), cardiopulmonary exercise test (CPET) variables and isokinetic muscle strength. Salbutamol 10 mug/min increased heart rate and blood pressure, while MSNA burst frequency remained unchanged. Peripheral chemosensitivity increased, as evidenced by an increased ventilatory response to hypoxia, but ventilatory responses to hypercapnia or muscle ischaemia remained unchanged. The effects of salbutamol 20 mug/min were similar. Both doses of salbutamol did not affect CPET. Only the higher dose of salbutamol decreased the anaerobic threshold, but this was not associated with a change in VO(2) max. Salbutamol increased the slopes of ventilation as a function of VO(2) (P < 0.05) and VCO(2) (P < 0.001) during CPET. Maximal isokinetic muscle strength was not affected by salbutamol. In conclusion, the acute administration of either low or high dose salbutamol does not affect exercise capacity in normal subjects, in spite of an earlier anaerobic threshold and increased chemosensitivity.
机译:据信β2-肾上腺素能受体激动剂具有人为产生特性。然而,这些药物的呼吸,心血管和肌肉综合作用如何影响运动能力仍未完全了解。在23名健康受试者中研究了沙丁胺醇的作用。这项研究是随机的,双盲安慰剂对照,并遵循交叉设计。沙丁胺醇的剂量为10杯/分钟(11位受试者),静脉注射20杯/分钟(其他12位受试者)。测量包括肌肉交感神经活动(MSNA),对高氧性高碳酸血症的通气反应(O(2,)中央化学反射中的7%CO(2)),等碳酸血症性低氧(N(2)中的10%O(2),周围性化学反射)等距肌肉收缩,然后是局部循环停搏(代谢不良),心肺运动试验(CPET)变量和等速肌力。沙丁胺醇10杯/分钟可增加心率和血压,而MSNA的爆发频率保持不变。周围化学敏感性增加,这表现为对缺氧的通气反应增加,但对高碳酸血症或肌肉缺血的通气反应保持不变。沙丁胺醇20杯/分钟的作用相似。两种剂量的沙丁胺醇均不影响CPET。只有更高剂量的沙丁胺醇降低了厌氧阈值,但这与VO(2)max的变化无关。沙丁胺醇在CPET期间增加了作为VO(2)(P <0.05)和VCO(2)(P <0.001)的函数的通气斜率。沙丁胺醇不影响最大等速肌力。总之,尽管较早的无氧阈值和增加的化学敏感性,低剂量或高剂量沙丁胺醇的急性给药都不会影响正常受试者的运动能力。

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