Journal of Applied Physiology AJP: Endocrinology and Metabolism
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J Appl Physiol (August 20, 2004). doi:10.1152/japplphysiol.00645.2004
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Submitted on June 22, 2004
Accepted on August 5, 2004

Effects on Breathing of Focal Acidosis at Multiple Medullary Raphe Sites in Awake Goats

Matthew R Hodges1*, Paul Martino1, Suzanne Davis1, Cynthia Opansky1, Lawrence G Pan2, and Hubert V Forster3

1 Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA
2 Department of Physical Therapy, Marquette University, Milwaukee, Wisconsin, USA
3 Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA; Zablocki VA Medical Center, Milwaukee, Wisconsin, USA

* To whom correspondence should be addressed. E-mail: mhodges46{at}hotmail.com.

Focal acidosis (FA) at single sites in the medullary raphe increases breathing during wakefulness (goats) and sleep (rats)(9, 22). Our aim was to determine the effects of FA at multiple medullary raphe sites in awake goats. FA at single (n=7) or multiple (n=6) sites was created through chronically implanted microtubules into midline raphe regions by microdialysis (MD) of mock cerebral spinal fluid (mCSF) equilibrated with 6.4% (pH=7.3), 50% (pH=6.5) or 80% (pH=6.3) CO2. We have previously shown that MD with a mCSF pH of 6.5 or 6.3, raphe tissue pH decreases by 0.1 and 0.18 respectively 200 µm from the MD site. These changes compare to the 0.06 decrease in the raphe pH with 7.5% inspired CO2 (11). MD with 6.4% CO2 at single or multiple sites had no effect on inspiratory flow (VI), tidal volume (VT), frequency (f), ventilatory drive (VT/TI), heart rate (HR), blood pressure or metabolic rate (VO2). MD at single sites with 80% CO2 increased VI (16.3 ± 4.9%), VT (16.9 ± 7.2%), and f (5.5 ± 1.5%) above control (P < 0.05). FA at multiple sites with either 50% or 80% CO2 increased VI by 18.4 ± 6.8% and 30.1 ± 7.4%, respectively (P < 0.05), where FA with 80% CO2 at multiple sites additionally increased VT, VT/TI, HR, VO2 and VCO2 (P < 0.05), highlighting the influence of the raphe on other physiologic functions in addition to breathing. We also noted hyperventilation (-2 mmHg, P < 0.005) with MD with 80% CO2 at multiple sites indicating that acidification has an effect on breathing independent of increasing metabolic rate. We conclude that: 1) under physiologic conditions the increase in breathing resulting from focal acidification is dependent upon the degree of acidification by increasing both CO2/H+, or the number of acidic foci and we speculate that the ventilatory response to inspired CO2 reflects a cumulative effect of stimulation of multiple chemoreceptor sites. Finally, we conclude that chemoreceptor stimulation affects multiple physiologic variables in addition to breathing.




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