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J Appl Physiol 92: 493-503, 2002; doi:10.1152/japplphysiol.00565.2001
8750-7587/02 $5.00
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Vol. 92, Issue 2, 493-503, February 2002

Sexually dimorphic effects of morphine and MK-801: sex steroid-dependent and -independent mechanisms

Deborah N. D'Souza1, Richard E. Harlan1,3, and Meredith M. Garcia2,3

Departments of 1 Structural and Cellular Biology and 2 Otolaryngology, and 3 Neuroscience Program, Tulane University School of Medicine, New Orleans, Louisiana 70112

Rats show gender differences in responses to morphine and the N-methyl-D-aspartate receptor antagonist dizocilpine (MK-801); the role of sex steroids in mediating these differences is unclear. We tested the overall hypothesis that circulating gonadal steroids determine the gender differences in morphine- and MK-801-induced behavior and c-Fos expression. Morphine caused a greater expression of c-Fos in the striatum of intact males than of that females, which was independent of sex steroids. MK-801 completely inhibited morphine-induced c-Fos in intact females but only caused partial inhibition in intact males; castrated males showed complete inhibition, which was reversed by testosterone, but gonadal steroids had no effect on this response in females. In thalamus, there was a large sex difference in the response to MK-801 that was independent of gonadal steroids. Behavioral responses to morphine were greater in males, but responses to MK-801 were greater in females; both were sex steroid independent. These findings show significant sex differences in response to morphine and MK-801 that are mediated by sex steroid-dependent and -independent mechanisms, which may be important in treatment outcomes of drug addiction.

immediate-early genes; c-Fos; striatum; thalamus; opiate-mediated behavior


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