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Department of Physiology and Biophysics, University of Calgary, Health Sciences Centre, Calgary, Alberta, Canada T2N 4N1
Experiments were carried
out to determine the threshold level of maternal nicotine that impairs
protective responses of rat pups to hypoxia.
From days 6 or 7 of
gestation, pregnant rats received either vehicle or nicotine (1.50, 3.00, or 6.00 mg of nicotine tartrate · kg body
wt
1 · day
1) or vehicle continuously
via a subcutaneous osmotic minipump. On postnatal days 5 or
6, pups were exposed to a single period of hypoxia produced
by breathing an anoxic gas mixture (97% N2 or 3%
CO2) and their time to last gasp was determined, or they were exposed to intermittent hypoxia and their ability to
autoresuscitate from hypoxic-induced primary apnea was determined.
Perinatal exposure to nicotine did not alter the time to last gasp or
the total number of gasps when the pups were exposed to a single period
of hypoxia. The number of successful autoresuscitations on repeated
exposure to hypoxia was, however, decreased in pups whose dams had
received either 3.00 or 6.00 mg of nicotine tartrate/kg body wt; these dosage regimens produced maternal serum nicotine concentrations of
19 ± 6 and 35 ± 8 ng/ml, respectively. Thus our experiments define the threshold level of maternal nicotine that significantly impairs protective responses of 5- to 6-day-old rat pups to
intermittent hypoxia such as may occur in human infants during episodes
of prolonged sleep apnea or positional asphyxia.
apnea; hypoxic gasping; perinatal drug exposure; sudden infant death syndrome
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