Shepherd A, Cleary M P
Am J Physiol. 1984 Feb;246(2 Pt 1):E123-8. doi: 10.1152/ajpendo.1984.246.2.E123.
Dehydroepiandrosterone (DHEA) is a known noncompetitive inhibitor of glucose-6-phosphate dehydrogenase (G6PD). In the present investigation, the effects of chronic DHEA treatment on G6PD and several other enzymes involved in lipid metabolism were examined in lean and obese Zucker rats. Significant decreases in body weight were found in DHEA-treated rats in comparison with nontreated rats. In lean rats, DHEA treatment did not decrease either liver or adipose tissue G6PD and fatty acid synthetase activity, but malic enzyme activity was increased. In obese rats, decreased liver and adipose tissue G6PD and fatty acid synthetase activities were found. Malic enzyme activity in liver of obese DHEA rats was increased but not in adipose tissue. Adipose tissue lipoprotein lipase activity was decreased in both lean and obese DHEA rats. Serum insulin in obese DHEA rats was also decreased compared with control obese rats. These results indicate that the inhibition of G6PD may not be the mechanism of action of the antiobesity effect of DHEA. However, the metabolic effects of DHEA seen in obese rats may contribute to its antiobesity action.
脱氢表雄酮(DHEA)是一种已知的葡萄糖-6-磷酸脱氢酶(G6PD)非竞争性抑制剂。在本研究中,研究了长期给予DHEA对瘦型和肥胖型 Zucker 大鼠体内G6PD及其他几种参与脂质代谢的酶的影响。与未处理的大鼠相比,DHEA处理的大鼠体重显著下降。在瘦型大鼠中,DHEA处理并未降低肝脏或脂肪组织中的G6PD及脂肪酸合成酶活性,但苹果酸酶活性增加。在肥胖大鼠中,肝脏和脂肪组织中的G6PD及脂肪酸合成酶活性降低。肥胖DHEA大鼠肝脏中的苹果酸酶活性增加,但脂肪组织中未增加。在瘦型和肥胖DHEA大鼠中,脂肪组织脂蛋白脂肪酶活性均降低。与对照肥胖大鼠相比,肥胖DHEA大鼠的血清胰岛素也降低。这些结果表明,抑制G6PD可能不是DHEA抗肥胖作用的作用机制。然而,在肥胖大鼠中观察到的DHEA的代谢效应可能有助于其抗肥胖作用。