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Center for Surgical Research and Department of Surgery, University of Alabama, Birmingham, Alabama 35294
Address all correspondence and requests for reprints to: Irshad H. Chaudry, Ph.D., Center for Surgical Research, Department of Surgery, University of Alabama, Volker Hall G094, 1670 University Boulevard, Birmingham, Alabama 35294. E-mail: irshad.chaudry{at}ccc.uab.edu
Immune responses are suppressed in males, but not in proestrous
females, after trauma-hemorrhage. Testosterone and 17ß-estradiol
appear to be responsible for divergent immune effects. There is
considerable evidence to suggest sex steroid hormone involvement in
immune functions. As formation of active steroid depends on the
activity of androgen- and estrogen-synthesizing enzymes, expression and
activity of 5
-reductase, aromatase, and 3ß- and 17ß-
hydroxysteroid dehydrogenases were determined in spleen and T
lymphocytes of male and proestrous female mice after trauma-hemorrhage.
All of the enzymes were present in spleen, specifically in T
lymphocytes. 5
-Reductase expression and activity increased in male T
lymphocytes, whereas aromatase activity, but not expression, increased
in female T lymphocytes. Increased 5
-reductase activity in male T
lymphocytes is immunosuppressive because of increased
5
-dihydrotestosterone synthesis, whereas in females increased
aromatase activity triggering 17ß-estradiol synthesis is
immunoprotective. This study also demonstrates the importance of
17ß-hydroxysteroid dehydrogenase oxidative and reductive functions.
The immunoprotection of proestrous females is associated with enhanced
reductase function of the enzyme. In males, decreased expression of
oxidative isomer type IV, which impairs catabolism of
5
-dihydrotestosterone, probably augments immunosuppression. This
study provides evidence for the involvement of intracrine sex steroid
synthesis in gender dimorphic immune responses after
trauma-hemorrhage.
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