Decreased 5alpha -dihydrotestosterone catabolism suppresses T lymphocyte functions in males after trauma-hemorrhage
Center for Surgical Research and Department of Surgery, University of Alabama School of Medicine, Birmingham, Alabama 35294 Trauma-hemorrhage produces profound immunosuppression in males but not in proestrus females. Prior castration or flutamide treatment of males following trauma-hemorrhage preven...
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Veröffentlicht in: | American Journal of Physiology: Cell Physiology 2002-06, Vol.282 (6), p.C1332-C1338 |
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Sprache: | eng |
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Zusammenfassung: | Center for Surgical Research and Department of Surgery,
University of Alabama School of Medicine, Birmingham, Alabama 35294
Trauma-hemorrhage produces
profound immunosuppression in males but not in proestrus females.
Prior castration or flutamide treatment of males following
trauma-hemorrhage prevents immunosuppression, implicating
5 -dihydrotestosterone for the immunosuppressive effects. 5 -Dihydrotestosterone, a high-affinity androgen receptor-binding steroid, is synthesized in tissues as needed and seldom accumulates. The presence of steroidogenic enzymes in T lymphocytes suggests both
synthesis and catabolism of 5 -dihydrotestosterone. We hypothesized, therefore, that the basis for high 5 -dihydrotestosterone activity in
T lymphocytes of males following trauma-hemorrhage is due to decreased
catabolism. Accordingly, catabolism of 5 -dihydrotestosterone was
assessed in splenic T lymphocytes by examining the activity and
expression of enzymes involved. Analysis showed increased synthesis and
decreased catabolism of 5 -dihydrotestosterone in intact male T
lymphocytes following trauma-hemorrhage. In contrast, reduced
5 -reductase activity and increased expression of
17 -hydroxysteroid dehydrogenase oxidative isomers suggest
inactivation of 5 -dihydrotestosterone in precastrated males. Thus
our study suggests increased synthesis and decreased catabolism of
5 -dihydrotestosterone as a reason for loss of T lymphocyte functions
in intact males following trauma-hemorrhage, as evidenced by decreased
release of interleukin-2 and -6.
gonadal steroids; androgen metabolism; cytokines |
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ISSN: | 0363-6143 1522-1563 |
DOI: | 10.1152/ajpcell.00560.2001 |