Istanbul University, Istanbul, Turkey.
Oxid Med Cell Longev. 2010 May-Jun;3(3):206-13. doi: 10.4161/oxim.3.3.11786.
Albumin represents the predominant circulating antioxidant agent in plasma exposed to continuous oxidative stress and a change in serum albumin structure accounts for its antioxidant properties. Alterations in the redox status of albumin may result in impairments of its biological properties. Alpha-lipoic acid (LA), a naturally occurring thiol compound found in virtually all species, is a potent antioxidant with high efficacy which is also involved in the chelation of metal ions, regeneration of antioxidants, and repair of oxidatively damaged proteins. In human body LA is rapidly reduced to dihydrolipoic acid (DHLA) after intake into the cell. Both, LA and DHLA are amphipathic molecules which act as antioxidants both in hydrophilic and lipophilic environments. The present study aimed to investigate the antioxidant/pro-oxidant effects of LA and DHLA due to their concentrations in metal-catalyzed protein oxidation (MCO) of human serum albumin (HSA). Progressive oxidative modification of albumin was found in MCO system by an increased content of protein hydroperoxides (POOH), protein carbonyl groups (PCO) which is the former's major breakdown product, and other protein oxidation markers such as advanced oxidized protein products (AOPP) and protein thiol groups (P-SH). The possible antioxidant protective effects of LA and DHLA were observed with 25 microM and 50 microM; DHLA being more influential. Protein oxidation parameters were found to be lower and P-SH levels seemed higher. However, prooxidant effects of both LA and DHLA came on the scene with increased concentrations of 75 microM and 100 microM where the latter seemed the most hazardous with contradicted results. It is clear that the loss of biological activity of human serum albumin by MCO system appears of medical relevance and if LA exerts similar effects seen in the present study, it is possible that cellular prooxidant activity can also result consuming this unique antioxidant in certain doses.
白蛋白是血浆中主要的循环抗氧化剂,在持续氧化应激下,血清白蛋白结构发生改变,从而产生其抗氧化特性。白蛋白的氧化还原状态的改变可能导致其生物学特性受损。α-硫辛酸(LA)是一种天然存在的硫醇化合物,几乎存在于所有物种中,是一种高效的抗氧化剂,它还参与金属离子的螯合、抗氧化剂的再生和氧化损伤蛋白质的修复。在人体内,LA 摄入细胞后迅速还原为二氢硫辛酸(DHLA)。LA 和 DHLA 都是两亲性分子,在亲水性和疏水性环境中均具有抗氧化作用。本研究旨在研究 LA 和 DHLA 的抗氧化/促氧化剂作用,因为它们的浓度会影响人血清白蛋白(HSA)的金属催化蛋白氧化(MCO)。在 MCO 体系中,白蛋白发生了渐进性氧化修饰,表现为蛋白质过氧化物(POOH)含量增加、蛋白质羰基(PCO)增加,这是前者的主要分解产物,以及其他蛋白质氧化标志物,如高级氧化蛋白产物(AOPP)和蛋白质巯基(P-SH)。发现 25 μM 和 50 μM 的 LA 和 DHLA 具有可能的抗氧化保护作用,DHLA 的影响更大。发现蛋白质氧化参数较低,P-SH 水平似乎较高。然而,LA 和 DHLA 的促氧化剂作用在浓度增加到 75 μM 和 100 μM 时出现,后者似乎危害更大,结果相互矛盾。很明显,MCO 系统导致人血清白蛋白的生物活性丧失具有医学相关性,如果 LA 产生了与本研究中相同的效果,那么在某些剂量下,细胞的促氧化剂活性也可能会导致这种独特的抗氧化剂的消耗。