Sofic E, Denisova N, Youdim K, Vatrenjak-Velagic V, De Filippo C, Mehmedagic A, Causevic A, Cao G, Joseph J A, Prior R L
Phytochemical Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA.
J Neural Transm (Vienna). 2001;108(5):541-57. doi: 10.1007/s007020170055.
The antioxidant and pro-oxidant capacity of catecholamines (CA) and related compounds were analyzed using the oxygen radical absorbance capacity (ORAC) assay. In the assay 2,2'-azobis (2-amidino-propane) dihydrochloride (AAPH), a peroxyl radical generator, ROO*; H2O2-Cu2+, mainly a hydroxyl radical generator, *OH; and Cu2+ a transition metal were used. The antioxidant effect of CA and its related compounds were in the order: neurotransmitters: dopamine (DA), norepinephrine (NE) > metabolites > amino acid precursors as measured by using AAPH. The antioxidant effect of CA and related compounds as measured by using AAPH were linearly correlated with concentration, while the antioxidant effect of CA in scavenging *OH produced by H2O2-Cu2+ increased proportionally to concentration at low concentration, but after reaching a maximum declined with increasing concentration. In the presence of Cu2+, CA acted as pro-oxidant. Glutathione (GSH) acted as a pro-oxidant when H2O2-Cu2+ or when Cu2+ alone was used as an oxidant and showed much higher pro-oxidant effect than DA, which could have relevance in the vulnerability of dopaminergic neurons to oxidative stress in the aging and aging related diseases. The antioxidant capacity of CA and many related compounds seems to be correlated with the numbers of hydroxyl groups and their position on the benzoic ring. The O-methylation and sulfate conjugation of the hydroxyl substitution inactivates both the antioxidant and pro-oxidant activities of CA. Our results show that oxidative stress induced by low (5 microM) or high (300 microM) doses H2O2 in pheochromocytoma PC12 cells significantly up-regulate the activity of Mg-dependent neutral sphingomyelinase (Sase), and significantly decreased GSH.
使用氧自由基吸收能力(ORAC)分析法分析了儿茶酚胺(CA)及其相关化合物的抗氧化和促氧化能力。在该分析中,使用了过氧自由基发生器2,2'-偶氮二(2-脒基丙烷)二盐酸盐(AAPH),ROO*;主要的羟基自由基发生器H2O2-Cu2+,OH;以及过渡金属Cu2+。通过使用AAPH测定,CA及其相关化合物的抗氧化作用顺序为:神经递质:多巴胺(DA)、去甲肾上腺素(NE)>代谢产物>氨基酸前体。使用AAPH测定时,CA及其相关化合物的抗氧化作用与浓度呈线性相关,而CA清除H2O2-Cu2+产生的OH的抗氧化作用在低浓度时与浓度成比例增加,但达到最大值后随浓度增加而下降。在Cu2+存在的情况下,CA起到促氧化剂的作用。当使用H2O2-Cu2+或单独使用Cu2+作为氧化剂时,谷胱甘肽(GSH)起到促氧化剂的作用,并且显示出比DA更高的促氧化作用,这可能与多巴胺能神经元在衰老及衰老相关疾病中对氧化应激的易感性有关。CA和许多相关化合物的抗氧化能力似乎与苯环上羟基的数量及其位置相关。羟基取代的O-甲基化和硫酸结合会使CA的抗氧化和促氧化活性均失活。我们的结果表明,低剂量(5 microM)或高剂量(300 microM)H2O2诱导的嗜铬细胞瘤PC12细胞中的氧化应激显著上调了镁依赖性中性鞘磷脂酶(Sase)的活性,并显著降低了谷胱甘肽(GSH)的水平。