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乙酰唑胺对 5050 米处脑血管功能和呼吸稳定性的影响。

Effects of acetazolamide on cerebrovascular function and breathing stability at 5050 m.

机构信息

Department of Physiology, Otago School of Medical Science, University of Otago, Dunedin, New Zealand.

出版信息

J Physiol. 2012 Mar 1;590(5):1213-25. doi: 10.1113/jphysiol.2011.219923. Epub 2012 Jan 4.

Abstract

One of the many actions of the carbonic anhydrase inhibitor, acetazolamide (ACZ), is to accelerate acclimatisation and reduce periodic breathing during sleep. The mechanism(s) by which ACZ may improve breathing stability, especially at high altitude, remain unclear. We tested the hypothesis that acute I.V. ACZ would enhance cerebrovascular reactivity to CO₂ at altitude, and thereby lower ventilatory drive and improve breathing stability during wakefulness. We measured arterial blood gases, minute ventilation (˙VE) and middle cerebral artery blood flow velocity (MCAv) before and 30 min following ACZ administration (I.V. 10 mg kg⁻¹) in 12 healthy participants at sea level and following partial acclimatisation to altitude (5050 m).Measures were made at rest and during changes in end-tidal PCO₂ and PO₂ (isocapnic hypoxia). At sea level, ACZ increased resting MCAv and its reactivity to both hypocapnia and hypercapnia (P < 0.05), and lowered resting VE, arterial O₂ saturation (Sa,O₂ ) and arterial PO₂ (Pa,O₂) (P < 0.05); arterial PCO₂ (Pa,CO₂ ) was unaltered (P > 0.05). At altitude, ACZ also increased resting MCAv and its reactivity to both hypocapnia and hypercapnia (resting MCAv and hypocapnia reactivity to a greater extent than at sea level). Moreover, ACZ at altitude elevated Pa,CO₂ and again lowered resting Pa,O₂ and Sa,O₂ (P <0.05). Although the ˙VE sensitivity to hypercapnia or isocapnic hypoxia was unaltered following ACZ at both sea level and altitude (P > 0.05), breathing stability at altitude was improved (e.g. lower incidence of ventilatory oscillations and variability of tidal volume; P < 0.05). Our data indicate that I.V. ACZ elevates cerebrovascular reactivity and improves breathing stability at altitude, independent of changes in peripheral or central chemoreflex sensitivities. We speculate that Pa,CO₂-mediated elevations in cerebral perfusion and an enhanced cerebrovascular reactivity may partly account for the improved breathing stability following ACZ at high altitude.

摘要

碳酸酐酶抑制剂乙酰唑胺 (ACZ) 的作用之一是加速适应和减少睡眠期间的周期性呼吸。ACZ 改善呼吸稳定性的机制(多个),特别是在高海拔地区,仍不清楚。我们检验了以下假设,即急性静脉内给予 ACZ 可增强高海拔时脑血管对 CO₂ 的反应性,从而降低通气驱动并改善清醒时的呼吸稳定性。我们在 12 名健康参与者中在海平面和部分适应高海拔(5050 米)后测量了动脉血气、分钟通气量(˙VE)和大脑中动脉血流速度(MCAv),在静脉内给予 ACZ(10mg/kg)前后 30 分钟。在休息时和在呼气末 PCO₂ 和 PO₂ 变化时(等碳酸缺氧)进行了测量。在海平面时,ACZ 增加了静息 MCAv 及其对低碳酸血症和高碳酸血症的反应性(P <0.05),并降低了静息 VE、动脉血氧饱和度(Sa,O₂)和动脉 PO₂(Pa,O₂)(P <0.05);动脉 PCO₂(Pa,CO₂)未改变(P >0.05)。在高海拔时,ACZ 还增加了静息 MCAv 及其对低碳酸血症和高碳酸血症的反应性(静息 MCAv 和低碳酸血症反应性比在海平面时更大)。此外,高海拔时的 ACZ 还升高了 Pa,CO₂,并再次降低了静息 Pa,O₂和 Sa,O₂(P <0.05)。尽管在海平面和高海拔时,ACZ 后对高碳酸血症或等碳酸缺氧的 ˙VE 敏感性没有改变(P >0.05),但高海拔时的呼吸稳定性得到改善(例如,降低了通气波动和潮气量变异性;P <0.05)。我们的数据表明,静脉内给予 ACZ 可升高脑血管反应性并改善高海拔时的呼吸稳定性,而外周或中枢化学感受器敏感性的变化则无关。我们推测,Pa,CO₂介导的脑灌注升高和增强的脑血管反应性可能部分解释了高海拔时 ACZ 后呼吸稳定性的改善。

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