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Department of Physiology, Faculty of Medicine and Health Science, University of Auckland, Auckland, New Zealand
We examined
developmental changes in breathing pattern and the ventilatory response
to hypoxia (7.4% O2) in unanesthetized Swiss CD-1 mice
ranging in age from postnatal day 0 to 42 (P0-P42) using head-out
plethysmography. The breathing pattern of
P0 mice was unstable. Apneas were frequent at
P0 (occupying 29 ± 6% of total time) but rare by
P3 (5 ± 2% of total time). Tidal volume increased in
proportion to body mass (~10-13 ml/kg), but increases in
respiratory frequency (f) (55 ± 7, 130 ± 13, and 207 ± 20 cycles/min for P0, P3, and
P42, respectively) were responsible for developmental increases in minute ventilation (690 ± 90, 1,530 ± 250, and 2,170 ± 430 ml · min
1 · kg
1
for P0, P3, and P42, respectively).
Between P0 and P3, increases in f were mediated
by reductions in apnea and inspiratory and expiratory times; beyond
P3, increases were due to reductions in expiratory time.
Mice of all ages showed a biphasic hypoxic ventilatory response, which
differed in two respects from the response typical of most mammals.
First, the initial hyperpnea, which was greatest in mature animals,
decreased developmentally from a maximum, relative to control, of 2.58 ± 0.29 in P0 mice to 1.32 ± 0.09 in P42
mice. Second, whereas ventilation typically falls to or below control
in most neonatal mammals, ventilation remained elevated relative to
control throughout the hypoxic exposure in P0 (1.73 ± 0.31), P3 (1.64 ± 0.29), and P9 (1.34 ± 0.17) mice but not in P19 or P42 mice.
respiration; apnea; plethysmography; in vivo
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