Mohan P F, Benghuzzi H
Department of Pathology, University of Mississippi Medical Center, Jackson 39206, USA.
Biomed Sci Instrum. 1997;33:550-5.
The steroid dehydroepiandrosterone (DHEA) is know to have anti-atherosclerotic properties. However, the mechanism by which DHEA exerts its effect is not clear. We hypothesized that DHEA protects against the atherogenic effects of LDL. Therefore attempts were made to test this hypothesis on endothelial cells (EC) in culture. Experiments were performed to determine the effect of DHEA and LDL on EC proliferation. Incubation of DHEA with EC for 24 hours had minimal effect on cell proliferation. However, at 48 hours of incubation, 25 and 50 nanograms DHEA inhibited EC proliferation by 50%. LDL (20 ug) inhibited EC proliferation by 27% and 63% at 24 and 48 hours respectively compared to the corresponding controls. EC proliferation was stimulated by 40% in the presence of 5 ng of DHEA and LDL in 24 hour incubations. However, at 48 hour incubations DHEA negated the inhibitory effect of LDL on EC proliferation. Determination of malondialdehyde (MDA), a measure of oxidative damage shows that in incubations of EC containing 5, 25, and 50 ng of DHEA for 24 hour did not affect the MDA levels. However, at 48 hour incubations, MDA levels were 44% and 50% higher respectively compared to the control. MDA levels increased in EC cultures containing LDL by 259% and 208% at 24 and 48 hours respectively compared to the corresponding controls. EC cultures containing LDL and 5 ng DHEA reduced MDA levels by 62% and 50% at 24 and 48 hours respectively compared to the corresponding controls. These results show that DHEA protects EC against LDL induced cytotoxic effect and suggests a mechanism for anti-atherosclerotic effect of DHEA.
类固醇脱氢表雄酮(DHEA)已知具有抗动脉粥样硬化特性。然而,DHEA发挥其作用的机制尚不清楚。我们推测DHEA可抵御低密度脂蛋白(LDL)的致动脉粥样硬化作用。因此,我们尝试在培养的内皮细胞(EC)上验证这一假设。进行实验以确定DHEA和LDL对EC增殖的影响。DHEA与EC孵育24小时对细胞增殖影响极小。然而,孵育48小时时,25纳克和50纳克的DHEA可使EC增殖抑制50%。与相应对照组相比,LDL(20微克)在24小时和48小时时分别使EC增殖抑制27%和63%。在24小时孵育中,5纳克的DHEA和LDL共同存在时可使EC增殖刺激40%。然而,在48小时孵育时,DHEA消除了LDL对EC增殖的抑制作用。丙二醛(MDA)是氧化损伤的一个指标,其测定结果显示,含有5纳克、25纳克和50纳克DHEA的EC孵育24小时并未影响MDA水平。然而,在48小时孵育时,MDA水平分别比对照组高44%和50%。与相应对照组相比,含有LDL的EC培养物在24小时和48小时时MDA水平分别增加259%和208%。与相应对照组相比,含有LDL和5纳克DHEA的EC培养物在24小时和48小时时分别使MDA水平降低62%和50%。这些结果表明,DHEA可保护EC免受LDL诱导的细胞毒性作用,并提示了DHEA抗动脉粥样硬化作用的一种机制。