First published online March 2, 2006
Journal of Experimental Biology 209, 1135-1146 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02106
Chronic hypercapnia modulates respiratory-related central pH/CO2 chemoreception in an amphibian, Bufo marinus
Afshan Gheshmy,
Robert Vukelich,
Angelo Noronha and
Stephen G. Reid*
The Centre for the Neurobiology of Stress, Department of Life
Sciences, University of Toronto at Scarborough, 1265 Military Trail, Toronto,
Ontario, M1C 1A4, Canada

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Fig. 1. Variables associated with fictive breathing recorded from the in
vitro brainstemspinal cord preparation at pH levels ranging from
7.4 to 8.2. (A) Fictive breath frequency; (B) episodes per minute; (C) breaths
per episode; (D) integrated vagal activity; (E) fictive breath duration. The
data are reported as the mean ± 1 s.e.m. *Significant difference from
the value at pH 8.2; significant difference between the
control and chronically hypercapnic groups. The solid bold line through the
data in A is a first order regression line (control,
r2=0.83; chronic hypercapnia,
r2=0.96). The dotted lines are 95% confidence
intervals.
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Fig. 3. Variables associated with breathing during a 9 day exposure to CHC in
vivo. (A) Breathing frequency; (B) episodes per minute; (C) breaths per
episode. *Significant difference from the day 0 value. The letter `a'
indicates a significant difference (on days 29) from the value on day
1.
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Fig. 5. The effects of chronic hypercapnia (CHC) (C,D) or control normocapnia (A,B)
on the breathing frequency response to acute hypercapnia in vivo with
the olfactory nerves intact (A,C) or denervated (B,D). The letters `a', `b'
and `c' indicate that the three values in each panel are significantly
different from one another. The asterisk in B indicates a significant
difference from the first air value (white bar).
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© The Company of Biologists Ltd 2006