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Vol. 296, Issue 1, 132-140, January 2001
Department of Pharmacology and Toxicology, Medical College of
Virginia of Virginia Commonwealth University, Richmond, Virginia
The present study conducted a comprehensive examination of the putative
sex differences in the potency of nicotine between male and female ICR
mice using several pharmacological and behavioral tests. Among the
responses to nicotine where significant sex differences were observed
are the antinociceptive and the anxiolytic effects of nicotine. Female
mice were found less sensitive to the acute effects of nicotine in
these tests after s.c. administration. Similar gender differences were
found after i.t. injection. Influence of gonadal hormones could
underlie sex differences observed in our studies. Indeed, our data
clearly indicate that sex hormones can modulate the effects of nicotine
and nicotinic receptors in a differential manner. Progesterone and
17
-estradiol were found to block nicotine's antinociception in
mice. Testosterone failed to do so. In addition, progesterone and
17
-estradiol blocked nicotine activation of
4
2 neuronal acetylcholine nicotinic
receptors expressed in oocytes. Our findings contribute
to our search for receptor mechanisms in drug dependence and in the
discovery of better pharmacological agents for nicotine dependence.
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