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Department of Physiology and Pharmacology, University of South Dakota School of Medicine, Vermillion, South Dakota 57069
Received 25 January 1996; accepted in final form 20 June 1996.
Schlenker, Evelyn H. Dextromethorphan affects
ventilation differently in male and female rats. J. Appl.
Physiol. 81(5): 1911-1916, 1996.
Subcutaneous administration
of aspartic acid results in a long-lasting but reversible depression of
ventilation in male but not in female rats. Aspartic acid acts on
N-methyl-D-aspartate receptors. The present study
tested the hypothesis that a noncompetitive N-methyl-D-aspartate-receptor antagonist,
dextromethorphan (Dex), would depress ventilation in female rats and
stimulate it in male rats. Moreover, Dex administered prior to aspartic
acid should prevent the aspartic acid-induced depression of ventilation
in male rats. In female rats, Dex caused a 30% depression of
ventilation relative to saline at 5 and 10 mg/kg (P < 0.01)
but not at the highest dose (20 mg/kg). In male rats, Dex had no effect
on ventilation. At a dose of 20 mg/kg, Dex depressed oxygen consumption
to 50% of the saline value at all time points in female rats
(P < 0.001) and in male rats 45 and 60 min
after administration. The time points when Dex depressed ventilation
and oxygen consumption were different in female rats, suggesting that
the depression of ventilation was not the result of a depression in
oxygen consumption. During a hypercapnic challenge (7%
CO2), female rats treated with 5 and 10 mg/kg of Dex
exhibited a smaller increase in ventilatory response relative to saline
treatment. At a dose of 20 mg/kg, the hypercapnic responsiveness of
male rats was markedly stimulated (85.8 ± 8.95 ml/min) relative to
saline (50.6 ± 9.14 ml/min; P < 0.001). Finally, Dex
administered before aspartic acid prevented the aspartic acid-induced depression of ventilation in male rats. Thus, in rats, Dex has gender-specific effects on ventilation and these effects are not associated with changes in oxygen consumption.
sex; oxygen consumption; N-methyl-D-aspartate receptor
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