Journal of Applied Physiology
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J Appl Physiol 96: 1745-1754, 2004. First published January 16, 2004; doi:10.1152/japplphysiol.00977.2003
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Effects of five consecutive nocturnal hypoxic exposures on the cerebrovascular responses to acute hypoxia and hypercapnia in humans

Jon C. Kolb,1 Philip N. Ainslie,2 Kojiro Ide,2 and Marc J. Poulin1,2,3

1Faculty of Kinesiology, Departments of 2Physiology and Biophysics and 3Clinical Neurosciences, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada T2N 4N1

Submitted 10 September 2003 ; accepted in final form 7 January 2004

The effects of discontinuous hypoxia on cerebrovascular regulation in humans are unknown. We hypothesized that five nocturnal hypoxic exposures (8 h/day) at a simulated altitude of 4,300 m (inspired O2 fraction = ~13.8%) would elicit cerebrovascular responses that are similar to those that have been reported during chronic altitude exposures. Twelve male subjects (26.6 ± 4.1 yr, mean ± SD) volunteered for this study. The technique of end-tidal forcing was used to examine cerebral blood flow (CBF) and regional cerebral O2 saturation (SrO2) responses to acute variations in O2 and CO2 twice before, immediately after, and 5 days after the overnight hypoxic exposures. Transcranial Doppler ultrasound was used to assess CBF, and near-infrared spectroscopy was used to assess SrO2. Throughout the nocturnal hypoxic exposures, end-tidal PCO2 decreased (P < 0.001) whereas arterial O2 saturation increased (P < 0.001) compared with overnight normoxic control measurements. Symptoms associated with altitude illness were significantly greater than control values on the first night (P < 0.001) and second night (P < 0.01) of nocturnal hypoxia. Immediately after the nocturnal hypoxic intervention, the sensitivity of CBF to acute variations in O2 and CO2 increased 116% (P < 0.01) and 33% (P < 0.05), respectively, compared with control values. SrO2 was highly correlated with arterial O2 saturation (R2 = 0.94 ± 0.04). These results show that discontinuous hypoxia elicits increases in the sensitivity of CBF to acute variations in O2 and CO2, which are similar to those observed during chronic hypoxia.

cerebral blood flow; cerebral O2 saturation; discontinuous hypoxia



Address for reprint requests and other correspondence: M. J. Poulin, Dept. of Physiology & Biophysics, Faculty of Medicine, Heritage Medical Research Bldg. Rm. 212, Univ. of Calgary, 3330 Hospital Drive NW, Calgary, Alberta, Canada T2N 4N1 (E-mail: poulin{at}ucalgary.ca).




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