Cr. Parker et Ba. Conwaymyers, THE EFFECTS OF DEHYDROEPIANDROSTERONE (DHEA) ON THE THYMUS, SPLEEN, AND ADRENALS OF PREPUBERTAL AND ADULT FEMALE RATS, Endocrine research, 24(2), 1998, pp. 113-126
Administration of dehydroepiandrosterone (DHEA) to female rats produce
s a condition of reproductive failure and ovarian cysts similar to tha
t seen in women having polycystic ovarian disease. On the other hand,
DHEA may have beneficial effects on the immune system We sought to det
ermine the effect of DHEA, when administered in pharmacological amount
s, on the thymus and spleen of prepubertal (25 day old) and young adul
t (60 day old) female rats. Since the adrenal, by means of its product
ion of corticosteroids, also is known to modulate the immune system, w
e also evaluated the effects of DHEA administration on this gland. The
daily SC administration of DHEA (6 mg/100g BW) to young adult female
rats led to progressive and striking reductions in thymic weights (gre
ater than 85% suppression after 20 days compared to vehicle treated an
imals). There were no effects of DHEA on body weights or the weights o
f the spleen. DHEA treatment also led to significantly reduced weights
of the adrenals which was sustained at about 15-20% below normal over
5-20 days treatment. Ovariectomy of the rats 5 days before initiation
of DHEA or vehicle treatment gave rise to significant increases in th
ymic and spleenic weights in control animals and strikingly blunted th
e inhibitory effects of DHEA treatment for 10 days on the thymus; DHEA
had no effect on the ovariectomy-induced rise in the weight of the sp
leen. Ovariectomy also had no effect on the inhibitory effects of DHEA
on adrenal weight. Similar, albeit quantitatively less striking, resp
onses were noted to occur after DHEA treatment in immature female rats
. These data indicate that DHEA in doses sufficient to interfere with
ovarian cyclicity also has potentially adverse effects on the adrenal
and thymus. The ovary appears to, play an independent role in maintena
nce of the size of the thymus and spleen and also may mediate some of
the effects of DHEA on the thymus but not those on the adrenals.