Journal
JOURNAL OF APPLIED PHYSIOLOGY
Volume 95, Issue 3, Pages 922-930Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00865.2002
Keywords
brain slice; intracellular recording; cardiorespiratory control; high-pressure nervous syndrome; hyperbaric helium; hypercapnia; hyperoxia; neuron
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Funding
- NHLBI NIH HHS [R01-HL-56683] Funding Source: Medline
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Neuronal sensitivity to pressure, barosensitivity, is illustrated by high-pressure nervous syndrome, which manifests as increased central nervous system excitability when heliox or trimix is breathed at >15 atmospheres absolute (ATA). We have tested the hypothesis that smaller levels of pressure (less than or equal to4 ATA) also increase neuronal excitability. The effect of hyperbaric helium, which mimics increased hydrostatic pressure, was determined on putative CO2/H+-chemoreceptor neurons in the solitary complex in rat brain stem slices by intracellular recording. Pressure stimulated firing rate in 31% of neurons (barosensitivity) and decreased input resistance. Barosensitivity was retained during synaptic blockade and was unaffected by antioxidants. Barosensitivity was distributed among CO2/H+-chemosensitive and -insensitive neurons; in CO2/H+-chemosensitive neurons, pressure did not significantly reduce neuronal chemosensitivity. We conclude that moderate pressure stimulates certain solitary complex neurons by a mechanism that possibly involves an increased cation conductance, but that does not involve free radicals. Neuronal barosensitivity to less than or equal to4 ATA may represent a physiological adaptive response to increased pressure or a pathophysiological response that is the early manifestation of high-pressure nervous syndrome.
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