Transient O2-dependent effects of CO2 on ventilation in the anesthetized mouse

• Autorzy: Pokorski M. , Izumizaki M. , Homma I.
• Języki publikacji: EN

Abstrakty

EN

In this study we sought to determine the effects of background hyperoxia on the ventilatory response to hypercapnia. We addressed this issue by examining the temporal profile of the first minute transients of minute ventilation, and its frequency and tidal components, in response to 5% and 10% CO2 each co-applied with the natural (balanced with air) and hyperoxic (balanced with O2) levels of oxygen. The study was performed on the urethane-anesthetized, tracheostomized, spontaneously breathing mouse, placed in a flow-through body plethysmograph. We identified an early suppressant effect of CO2-in-O2 on breathing frequency. The frequency declined to 88.5 ±1.4% and 87.8 ±1.9% relative to the pre-test, baseline level for 5% and 10% CO2, respectively. There was a compensatory rise in tidal volume and no major change in the overall ventilation. In contrast, CO2-in-Air resulted in ventilatory stimulation caused in equal measure by frequency and tidal components. Thus, the inhibitory effect on breathing frequency of the CO2-in-O2 resulted from the O2 content in the mixture and had the temporal characteristics consistent with carotid body function. In conclusion, transient O2-dependent effects can bear on the nascent hypercapnic ventilatory response. The complexity of the O2-CO2 interaction regarding the breathing pattern components should be taken into account while designing the optimal conditions for a hypercapnic test.

Słowa kluczowe

EN

hypercapnia; mouse; breathing frequency; mice; ventilation; ventilatory response; hyperoxia; hypercapnic ventilatory response; carotid body; chemoreceptor

• Wydawca: -
• Czasopismo: Journal of Physiology and Pharmacology
• Rocznik: 2005
• Tom: 56
• Numer: 3
• Opis fizyczny: p.447-454,fig.,ref.

Twórcy

autor

Pokorski M.

• Polish Academy of Sciences, 5 Pawinskiego St., 02-929 Warsaw, Poland

autor

Izumizaki M.

autor

Homma I.