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Original Studies |
Max-Planck-Institute of Psychiatry (A.S., J.M., E.F., D.M.H., F.H., T.P.), D-80804 München, Germany; and Max-Planck-Institute of Immunobiology (C.G.), D-79108 Freiburg, Germany
Address all correspondence and requests for reprints to: Andreas Schuld, M.D., Max-Planck-Institute of Psychiatry, Kraepelinstraße 10, D-80804 Munich, Germany. E-mail: schuld{at}mpipsykl.mpg.de
Dehydroepiandrosterone (DHEA) and
DHEA-sulfate (DHEA-S) have immunomodulatory
effects in vitro and in vivo.
Additionally, their plasma levels are altered during chronic infection
and inflammation. However, it remains unknown whether these steroids
are involved in early host responses to infection in humans. We
examined DHEA and DHEA-S levels during
experimental endotoxinemia, a well established pathophysiological model
of bacterial infections in humans. Purified Salmonella abortus
equi endotoxin (0.2, 0.4, or 0.8 ng/kg body weight) was
injected in a single-blind, placebo-controlled experiment to 17 healthy
male volunteers. During the following 12 h, rectal temperature and
the plasma levels of ACTH, cortisol, DHEA,
DHEA-S, interleukin 6, and tumor necrosis factor
were
determined. Confirming earlier studies, temperature and cytokine levels
showed monophasic, dose-dependent increases in response to endotoxin.
In contrast, endocrinological effects of endotoxin showed a complex,
biphasic pattern: cortisol levels were not affected by 0.2 ng/kg but
significantly increased during the first 6 h following 0.4 and 0.8
ng/kg endotoxin, whereas ACTH and DHEA levels were
significantly enhanced during the first 6 h following 0.8 ng/kg
only. ACTH, DHEA, and cortisol secretion was blunted 612
h following 0.8 ng/kg. DHEA-S levels were unaffected
during the first 6 h following all dosages, but between 612 h
after injection they were significantly increased following 0.2 ng/kg,
unaffected by 0.4 ng/kg, and significantly decreased following 0.8
ng/kg endotoxin. The present results suggest that similarly to
glucocorticoids, the adrenal androgens DHEA and
DHEA-S play an important role during early host responses
to bacterial infections in humans.
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