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Am J Physiol Endocrinol Metab 276: E196-E204, 1999;
0193-1849/99 $5.00
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Vol. 276, Issue 1, E196-E204, January 1999

DHEA improves glucose uptake via activations of protein kinase C and phosphatidylinositol 3-kinase

Tatsuo Ishizuka, Kazuo Kajita, Atsushi Miura, Masayoshi Ishizawa, Yoshinori Kanoh, Satomi Itaya, Mika Kimura, Naoya Muto, Tomoatsu Mune, Hiroaki Morita, and Keigo Yasuda

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-alpha , -beta , and -gamma . DHEA provoked the translocation of PKC-beta and -zeta 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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