Journal of Applied Physiology AJP: Gastrointestinal and Liver Physiology
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J Appl Physiol 89: 1333-1339, 2000;
8750-7587/00 $5.00
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Vol. 89, Issue 4, 1333-1339, October 2000

Neurocirculatory consequences of intermittent asphyxia in humans

Ailiang Xie1, James B. Skatrud1, David C. Crabtree1, Dominic S. Puleo1, Brian M. Goodman2, and Barbara J. Morgan3

Departments of 1 Medicine and 3 Surgery, University of Wisconsin, and the 2 William S. Middleton Veterans Hospital, Madison, Wisconsin 53705

We examined the neurocirculatory and ventilatory responses to intermittent asphyxia (arterial O2 saturation = 79-85%, end-tidal PCO2 =3-5 Torr above eupnea) in seven healthy humans during wakefulness. The intermittent asphyxia intervention consisted of 20-s asphyxic exposures alternating with 40-s periods of room-air breathing for a total of 20 min. Minute ventilation increased during the intermittent asphyxia period (14.2 ± 2.0 l/min in the final 5 min of asphyxia vs. 7.5 ± 0.4 l/min in baseline) but returned to the baseline level within 2 min after completion of the series of asphyxic exposures. Muscle sympathetic nerve activity increased progressively, reaching 175 ± 12% of baseline in the final 5 min of the intervention. Unlike ventilation, sympathetic activity remained elevated for at least 20 min after removal of the chemical stimuli (150 ± 10% of baseline in the last 5 min of the recovery period). Intermittent asphyxia caused a small, but statistically significant, increase in heart rate (64 ± 4 beats/min in the final 5 min of asphyxia vs. 61 ± 4 beats/min in baseline); however, this increase was not sustained after the return to room-air breathing. These data demonstrate that relatively short-term exposure to intermittent asphyxia causes sympathetic activation that persists after removal of the chemical stimuli. This carryover effect provides a potential mechanism whereby intermittent asphyxia during sleep could lead to chronic sympathetic activation in patients with sleep apnea syndrome.

sympathetic nervous system; hypoxia; hypercapnia


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