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β受体阻滞剂导致肌肉疲劳增加的因素。

Factors contributing to increased muscle fatigue with beta-blockers.

作者信息

McKelvie R S, Jones N L, Heigenhauser G J

机构信息

McMaster University Health Sciences Centre, Hamilton, Ont., Canada.

出版信息

Can J Physiol Pharmacol. 1991 Feb;69(2):254-61. doi: 10.1139/y91-039.

Abstract

beta-Adrenoceptor blockers are widely used clinically and can be classified as nonselective (beta 1 and beta 2) or selective (beta 1). Impairment of exercise performance is a well-known side effect of this group of drugs. This paper reviews mechanisms that could potentially be responsible for this impairment. In addition to cardiovascular and metabolic effects, beta-blockade inhibits Na(+)-K+ ATPase pumps controlling ion movement between muscle and plasma and thus may contribute to muscle fatigue through this mechanism. To investigate the relationship between the change in plasma [K+] and exercise performance, we studied healthy male subjects taking propranolol. Eight subjects performed maximal incremental cycle ergometer exercise tests during control (no drug), low dose (LD) (40 mg daily), and high dose (HD) (265 +/- 4.3 (SE) mg daily) of propranolol. The control plasma [K+] (5.8 +/- 0.12 mequiv./L) during exercise was significantly lower than either the LD (6.4 +/- 0.05 mequiv./L) or HD (6.1 +/- 0.16 mequiv./L) values. There was no significant difference between plasma [K+] for the LD and HD of propranolol. However, maximum oxygen uptake was reduced only while taking the HD of propranolol. Six of the subjects also performed three 30-s bouts of high intensity exercise on an isokinetic cycle ergometer while taking the LD and HD of propranolol. There was no significant difference between doses for the increase in plasma [K+] (LD, 7.8 +/- 0.35 mequiv./L vs. HD, 7.6 +/- 0.36 mequiv./L) during exercise. However, exercise performance was significantly reduced during HD compared with LD. These results suggest that the increases in plasma [K+] with propranolol did not play a direct significant role in the reduced performance observed during the HD.

摘要

β-肾上腺素受体阻滞剂在临床上广泛应用,可分为非选择性(β1和β2)或选择性(β1)。运动能力受损是这类药物众所周知的副作用。本文综述了可能导致这种损害的机制。除了心血管和代谢作用外,β受体阻滞剂抑制控制肌肉与血浆之间离子移动的钠钾ATP酶泵,因此可能通过这种机制导致肌肉疲劳。为了研究血浆[K+]变化与运动能力之间的关系,我们对服用普萘洛尔的健康男性受试者进行了研究。8名受试者在对照(未用药)、低剂量(LD)(每日40毫克)和高剂量(HD)(每日265±4.3(SE)毫克)普萘洛尔状态下进行了最大递增式自行车测力计运动试验。运动期间对照血浆[K+](5.8±0.12毫当量/升)显著低于LD(6.4±0.05毫当量/升)或HD(6.1±0.16毫当量/升)值。普萘洛尔LD和HD的血浆[K+]之间无显著差异。然而,仅在服用普萘洛尔HD时最大摄氧量降低。6名受试者在服用普萘洛尔LD和HD时还在等动自行车测力计上进行了3次30秒的高强度运动。运动期间血浆[K+]升高幅度(LD,7.8±0.35毫当量/升对HD,7.6±0.36毫当量/升)在不同剂量之间无显著差异。然而,与LD相比,HD期间运动能力显著降低。这些结果表明,普萘洛尔导致的血浆[K+]升高在HD期间观察到的运动能力降低中未起直接显著作用。

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