Nylander E, Dahlström U
Eur J Appl Physiol Occup Physiol. 1984;53(1):48-52. doi: 10.1007/BF00964689.
Previous studies have shown that the intrinsic heart rate (IHR) may undergo changes, e.g., decrease after long-term endurance training. The mechanism for this adaptation is not known. In this study, rats were subjected to long-term oral treatment with the beta receptor stimulating drug prenalterol. During the treatment period heart rates at rest and during submaximal exercise were measured. Heart rate after 30 min rest and also 2 min after exercise was higher in the treated animals, due to the beta stimulation. The treated rats had a significantly lower heart rate increase during exercise than untreated controls, consistent with a partial beta-blocking effect of the drug in states with a high endogenous sympathetic activity. Therefore, the animals were not trained but only exposed to the increased stimulation of cardiac beta receptors accomplished by the drug while at rest. After 25 weeks, prenalterol was withdrawn and the IHR was measured in situ after a denervation procedure. The treatment with prenalterol had not altered the IHR. Our previous results from training studies indicate that a heart rate increase above a certain level or the stimulation for a lower setting of the IHR as seen after endurance training. In this study chronic beta receptor stimulation with prenalterol did not influence the IHR, which supports that hypothesis.
先前的研究表明,固有心率(IHR)可能会发生变化,例如长期耐力训练后会降低。这种适应性的机制尚不清楚。在本研究中,对大鼠进行了β受体激动剂普瑞特罗的长期口服治疗。在治疗期间,测量了静息心率和次最大运动时的心率。由于β刺激,治疗组动物在休息30分钟后以及运动2分钟后的心率较高。与未治疗的对照组相比,治疗组大鼠在运动期间的心率增加明显较低,这与该药物在高内源性交感神经活动状态下的部分β受体阻滞作用一致。因此,这些动物并未接受训练,只是在休息时受到药物引起的心脏β受体刺激增加的影响。25周后,停用普瑞特罗,并在去神经支配手术后原位测量IHR。普瑞特罗治疗并未改变IHR。我们先前训练研究的结果表明,心率增加超过一定水平或如耐力训练后所见的对较低IHR设定值的刺激。在本研究中,普瑞特罗对β受体的慢性刺激并未影响IHR,这支持了该假设。