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The Third Department of Internal Medicine, Gifu University School of Medicine, Gifu 500, Japan
We have examined the
effect of adrenal androgen, dehydroepiandrosterone (DHEA), on glucose
uptake, phosphatidylinositol (PI) 3-kinase, and protein kinase C (PKC)
activity in rat adipocytes. DHEA (1 µM) provoked a twofold increase
in 2-[3H]deoxyglucose
(DG) uptake for 30 min. Pretreatment with DHEA increased
insulin-induced
2-[3H]DG uptake
without alterations of insulin specific binding and autophosphorylation
of insulin receptor. DHEA also stimulated PI 3-kinase activity.
[3H]DHEA bound to
purified PKC containing PKC-
, -
, and -
. DHEA provoked the
translocation of PKC-
and -
from the cytosol to the membrane in
rat adipocytes. These results suggest that DHEA stimulates both PI
3-kinase and PKCs and subsequently stimulates glucose uptake. Moreover,
to clarify the in vivo effect of DHEA on Goto-Kakizaki (GK) and Otsuka
Long-Evans fatty (OLETF) rats, animal models of non-insulin-dependent
diabetes mellitus (NIDDM) were treated with 0.4% DHEA for 2 wk.
Insulin- and 12-O-tetradecanoyl phorbol-13-acetate-induced
2-[3H]DG uptakes of
adipocytes were significantly increased, but there was no significant
increase in the soleus muscles in DHEA-treated GK/Wistar or
OLETF/Long-Evans Tokushima (LETO) rats when compared with untreated
GK/Wistar or OLETF/LETO rats. These results indicate that in vivo DHEA
treatment can result in increased insulin-induced glucose uptake in two
different NIDDM rat models.
dehydroepiandrosterone; non-insulin-dependent diabetes mellitus; 2-deoxyglucose
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