Easton P A, Anthonisen N R
Department of Medicine, University of Manitoba, Winnipeg, Canada.
J Appl Physiol (1985). 1988 Apr;64(4):1445-50. doi: 10.1152/jappl.1988.64.4.1445.
During sustained hypoxia the decline in ventilation that occurs in normal adult humans may be related to central accumulation of a neurochemical with net inhibitory effect. Recent investigations have shown that the putative neurotransmitter adenosine can effect a prolonged respiratory inhibition. Therefore we evaluated the possible role of adenosine in the hypoxia ventilatory decline by employing aminophylline as an adenosine blocker. We evaluated the ventilatory response to 25 min of sustained hypoxia (80% arterial O2 saturation), in eight young adults after pretreatment with either intravenous saline or aminophylline. With a mean serum aminophylline level of 15.7 mg/l, over 25 min of sustained hypoxia, peak hypoxic ventilation decreased by only 12.8% compared with 24.8% with saline, a significant difference. However, the ventilatory decline during sustained hypoxia was not abolished by the aminophylline pretreatment. Unlike the usual tidal volume-dependent attenuation of hypoxic ventilation exhibited after saline, after aminophylline the ventilatory decline was achieved predominantly through alterations in respiratory timing. Thus aminophylline pretreatment did alleviate the hypoxic ventilatory decline, although the associated alterations in breathing pattern were uncharacteristic. We conclude that adenosine may play a contributing role in the hypoxic ventilatory decline.
在持续性低氧期间,正常成年人出现的通气量下降可能与具有净抑制作用的神经化学物质在中枢的蓄积有关。最近的研究表明,假定的神经递质腺苷可产生长时间的呼吸抑制作用。因此,我们通过使用氨茶碱作为腺苷阻断剂,评估了腺苷在低氧通气量下降中可能发挥的作用。我们在8名年轻成年人中,分别在静脉注射生理盐水或氨茶碱预处理后,评估了他们对25分钟持续性低氧(动脉血氧饱和度80%)的通气反应。在平均血清氨茶碱水平为15.7毫克/升的情况下,在25分钟的持续性低氧期间,与生理盐水组相比,低氧通气峰值仅下降了12.8%,而生理盐水组下降了24.8%,差异显著。然而,氨茶碱预处理并未消除持续性低氧期间的通气量下降。与生理盐水处理后通常出现的依赖潮气量的低氧通气减弱不同,氨茶碱处理后通气量下降主要是通过呼吸时间的改变实现的。因此,氨茶碱预处理确实减轻了低氧通气量下降,尽管呼吸模式的相关改变并不典型。我们得出结论,腺苷可能在低氧通气量下降中起一定作用。