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Vol. 282, Issue 2, 769-778, 1997
Department of Psychology, Washington State University, Pullman,
Washington
Previous studies indicate that mu opioid agonists such as
morphine may produce greater antinociception in male than in female rodents. The present study was designed to investigate the generality of this finding across dose, time and type of opioid agonist. In adult
female and male Sprague-Dawley rats, time-effect curves were obtained
for vehicle and three doses each of the mu agonists fentanyl
and buprenorphine, the kappa agonists
(5
,7
,8
)-(
)-N-methyl-[7-(1-pyrrolidinyl)-1-oxaspiro(4,5)dec-8-yl]benzeneacetamide (U69,593) and bremazocine and the delta agonists
[D-Pen2,D-Pen5]enkephalin
(DPDPE) and deltorphin on the 52°C hot-plate and tail-withdrawal (immersion) assays. There were sex differences in the antinociceptive effects of the two kappa agonists and the two
delta agonists, but the differences were assay-, dose-
and/or time-dependent. Peak effects of U69,593 on tail withdrawal and
DPDPE on hot plate tended to occur earlier in females than in males,
and bremazocine produced greater tail-withdrawal antinociception in
females than in males, whereas the highest doses of the two
delta opioids produced greater hot-plate antinociception in
males than in females. These results contrast with several previous
reports showing that male rodents are more sensitive than females to
the antinociceptive effects of mu and kappa (but
not delta) opioids. These discrepancies may be caused by the
more comprehensive examination of sex differences across dose and time
used in the present study; sex differences that are dose- or
time-dependent may not be apparent if a single dose or time point is
examined. In addition, repeated testing procedures used in the present
study may produce different results than acute testing procedures
would, if female and male rats develop opioid tolerance at different
rates.
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