Hespel P, Lijnen P, Vanhees L, Fagard R, Fiocchi R, Moerman E, Amery A
Med Sci Sports Exerc. 1986 Apr;18(2):186-91.
The effect of beta 1- or beta 2-antagonism on the plasma levels of glucose, lactate, triglycerides, and free fatty acids was studied in seventeen normal male volunteers. All subjects performed three graded and uninterrupted exercise tests until exhaustion. Prior to each exercise test they received in a randomized order during three consecutive days either placebo or a predominant beta 1-blocker (atenolol, 50 mg once per day) or a predominant beta 2-blocker (ICI 118,551, 20 mg t.i.d.), according to a double-blind cross-over study design. Atenolol increased the plasma level of glucose at rest but did not influence the rise in plasma glucose during exercise. ICI 118,551 did not change the resting plasma glucose level, but it prevented the exercise-induced rise in plasma glucose, observed during placebo. During beta 1-antagonism the plasma lactate concentration at rest and during or after exercise was not different from placebo. During beta 2-blockade the exercise-induced rise in plasma lactate tended to be suppressed, and during recovery the plasma lactate levels were significantly lower than during placebo. The serum triglycerides concentration at rest and exercise was not altered, either by beta 1- or by beta 2-antagonism. Atenolol and ICI 118,551 did not affect the serum level of free fatty acids at rest, but at moderate exercise the serum free fatty acids concentration was lower during beta 1-blockade than during placebo. Our results provide further evidence that beta 2-adrenergic receptors are involved in the regulation of the plasma levels of glucose and lactate during exercise.
在17名正常男性志愿者中研究了β1或β2受体拮抗作用对血浆葡萄糖、乳酸、甘油三酯和游离脂肪酸水平的影响。所有受试者进行了三次分级且不间断的运动测试,直至精疲力竭。在每次运动测试前,根据双盲交叉研究设计,他们在连续三天内按随机顺序接受安慰剂、主要的β1受体阻滞剂(阿替洛尔,每天50毫克,每日一次)或主要的β2受体阻滞剂(ICI 118,551,20毫克,每日三次)。阿替洛尔使静息时血浆葡萄糖水平升高,但不影响运动期间血浆葡萄糖的升高。ICI 118,551未改变静息时血浆葡萄糖水平,但它阻止了运动诱导的血浆葡萄糖升高,这在安慰剂组中可以观察到。在β1受体拮抗期间,静息时以及运动期间或运动后的血浆乳酸浓度与安慰剂组无差异。在β2受体阻滞期间,运动诱导的血浆乳酸升高趋于被抑制,并且在恢复期间血浆乳酸水平显著低于安慰剂组。β1或β2受体拮抗均未改变静息和运动时的血清甘油三酯浓度。阿替洛尔和ICI 118,551不影响静息时血清游离脂肪酸水平,但在中等强度运动时,β1受体阻滞期间血清游离脂肪酸浓度低于安慰剂组。我们的结果提供了进一步的证据,表明β2肾上腺素能受体参与运动期间血浆葡萄糖和乳酸水平的调节。