Richalet J P, Le-Trong J L, Rathat C, Merlet P, Bouissou P, Keromes A, Veyrac P
Institut National de la Santé et de la Recherche Médicale U138 et U296, Faculté de Médecine, Créteil, France.
J Appl Physiol (1985). 1989 Aug;67(2):523-7. doi: 10.1152/jappl.1989.67.2.523.
A decrease in heart rate response to isoproterenol (IP) infusion has been previously described in humans exposed to acute (2-3 days) or chronic (21 days) exposure to altitude hypoxia (J. Appl. Physiol. 65: 1957-1961, 1988). To evaluate this cardiac response in subacute (8 days) hypoxia and to explore its reversal with restoration of normoxia, six subjects received an IP infusion under normoxia (condition N), after 8 days in altitude (4,350 m, condition H8), on the same day in altitude after inhalation of O2 restoring normoxic arterial O2 saturation (SaO2, condition HO), and 6-11 h (condition RN) and 4-5 mo (condition ND) after the return to sea level. Cardiac chronotropic response to IP, evaluated by the mean increase in heart rate from base value (delta HR, min-1), was lower in condition H8 [mean 30 +/- 13 (SD)] than in condition N (50 +/- 14, P less than 0.03); it was slightly higher in condition HO (38 +/- 14) or condition RN (42 +/- 15) than condition H8 but still significantly different from condition N (P less than 0.03), despite normal values of SaO2. delta HR in condition ND (55 +/- 10) returned to base N value. These findings confirm the hypothesis of a hypoxia-induced decrease in cardiac chronotropic function. Two possible mechanisms are suggested: an O2-dependent one, rapidly reversible with recent restoration of normoxia, and a more slowly reversible mechanism, probably a downregulation of the cardiac beta-receptors.
先前已有研究表明,暴露于急性(2 - 3天)或慢性(21天)高原低氧环境的人类,对异丙肾上腺素(IP)输注的心率反应会降低(《应用生理学杂志》65: 1957 - 1961, 1988)。为评估亚急性(8天)低氧环境下的心脏反应,并探究恢复常氧后这种反应的逆转情况,6名受试者在常氧状态下(N状态)接受IP输注,在海拔4350米处停留8天后(H8状态)接受IP输注,在海拔处吸入氧气恢复常氧动脉血氧饱和度(SaO2)当天(HO状态)接受IP输注,以及在返回海平面后6 - 11小时(RN状态)和4 - 5个月(ND状态)接受IP输注。通过心率相对于基础值的平均增加幅度(δHR,次/分钟)评估的心脏变时性反应,在H8状态下[平均30 ± 13(标准差)]低于N状态(50 ± 14,P < 0.03);在HO状态(38 ± 14)或RN状态(42 ± 15)下略高于H8状态,但仍与N状态有显著差异(P < 0.03),尽管SaO2值正常。ND状态下的δHR(55 ± 10)恢复到了基础N值。这些发现证实了低氧诱导心脏变时功能降低的假说。提出了两种可能的机制:一种是依赖氧气的机制,近期恢复常氧后可迅速逆转;另一种是逆转较慢的机制,可能是心脏β受体的下调。