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Increased chemoreceptor output and ventilatory response to sustained hypoxia
D Georgopoulos1, S Walker, N R Anthonisen
1Department of Medicine, University of Manitoba, Winnipeg, Canada.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|September 1, 1989
Summary
Selective stimulation of peripheral chemoreceptors with almitrine enhances the biphasic ventilatory response to sustained hypoxia in humans. This involves a greater initial increase and subsequent decline in ventilation during hypoxic conditions.
Area of Science:
- Physiology
- Respiratory Control
- Neuroscience
Background:
- The human ventilatory response to sustained hypoxia (VRSH) is biphasic: an initial increase from peripheral chemoreceptors followed by a central hypoxic depression.
- Understanding the role of peripheral chemoreceptors in this pattern is crucial for respiratory control research.
Purpose of the Study:
- To investigate the impact of selectively stimulating peripheral chemoreceptors on the biphasic VRSH pattern.
- To evaluate the ventilatory response to hypoxia after pretreatment with almitrine, a known peripheral chemoreceptor stimulant.
Main Methods:
- Eight subjects underwent a single-blind study with almitrine (75 mg) or placebo pretreatment.
- Ventilatory responses were measured during sequential exposure to room air, oxygen, and sustained hypoxia (SaO2 = 80%) with constant end-tidal CO2.
- Inspiratory minute ventilation and breathing patterns were analyzed during different phases of the protocol.
Main Results:
- The VRSH remained biphasic regardless of pretreatment.
- Almitrine pretreatment significantly amplified the initial ventilatory increase during hypoxia compared to placebo (14.2 vs. 4.6 L/min).
- The subsequent decline in ventilation during hypoxia was also significantly greater after almitrine administration.
Conclusions:
- Selective peripheral chemoreceptor stimulation with almitrine potentiates both the initial and subsequent phases of the ventilatory response to sustained hypoxia.
- This suggests a significant role for peripheral chemoreceptor drive in modulating the overall pattern of the human hypoxic ventilatory response.