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Center for Surgical Research and Department of Surgery, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama 35294
Submitted 30 December 2002 ; accepted in final form 7 April 2003
Studies indicate that administration of the adrenal steroid
dehydroepiandrosterone (DHEA) after trauma-hemorrhage in male mice improved
cellular immune functions and reduced mortality rates from subsequent sepsis.
There is evidence, however, that DHEA is converted to estrogens in males and
that estrogens are immunoprotective after trauma-hemorrhage (TH). In contrast,
DHEA in females can be converted to testosterone that has deleterious effects
on immune functions. The aim of our study, therefore, was to determine whether
administration of DHEA in proestrus females after TH would deteriorate immune
responses. Proestrus female C3H/HeN mice (age 78 wk) were subjected to
laparotomy (i.e., soft tissue trauma induced) and hemorrhagic shock (35
± 5 mmHg for 90 min) or sham operation. The mice then received DHEA
(100 µ/25 g body wt) or vehicle subcutaneously followed by fluid
resuscitation (4x the shed blood volume). Plasma IL-6, splenocyte
proliferation, splenocyte IL-2, IL-3, IFN-
, IL-10 release, and splenic
M
IL-1
, IL-6, IL-10, and IL-12 release were determined 24 h after
TH. Plasma IL-6 levels were significantly increased in vehicle-treated
females, and DHEA administration markedly attenuated this response. In
vehicle-treated females, splenocyte proliferation, IL-2, IL-3, and IFN-
release, and splenic M
IL-1
, IL-6, and IL-12 release were
maintained or slightly enhanced after TH. In DHEA-treated females, however,
these immune functional parameters were either unaltered compared with
vehicle-treated animals or even further enhanced, but surprisingly were not
depressed. Moreover, DHEA reduced splenocyte and splenic M
anti-inflammatory cytokine (i.e., IL-10) production after TH compared with
vehicle-treated females. Because DHEA further enhances the immune
responsiveness in proestrus females after TH, this hormone might be a useful
adjunct even in females for further enhancing immune responses and decreasing
the mortality rate after trauma and severe blood loss.
inflammation; cytokines; gender
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