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在一氧化氮存在的情况下,2-羟基雌激素和4-羟基雌激素在体外生成过氧亚硝酸盐。

In vitro generation of peroxynitrite by 2- and 4-hydroxyestrogens in the presence of nitric oxide.

作者信息

Paquette B, Cantin A M, Kocsis-Bédard S, Barry S, Lemay R, Jay-Gerin J P

机构信息

Département de Médecine Nucléaire et de Radiobiologie, Faculté de Médecine, Université de Sherbrooke, Sherbrooke, Québec J1H 5N4, Canada.

出版信息

Chem Res Toxicol. 2001 May;14(5):547-54. doi: 10.1021/tx0001934.

Abstract

Estrogen metabolism is altered in most, if not all, breast cancer tumors. These alterations primarily lead to the formation of the catechol estrogen metabolites, 2- and 4-hydroxyestrogens, which can generate superoxide anion radicals (O(2)()(-)) through the redox cycling of semiquinone/quinone derivatives. In breast cancer cells, the activity of nitric oxide synthase is also frequently elevated, resulting in an increased level of exposure to nitric oxide (()NO). Since ()NO rapidly reacts with O(2)()(-) to produce the peroxynitrite anion (ONOO(-)), this study was undertaken to determine whether ONOO(-) can be generated when 2- and 4-hydroxyestrogens are incubated in vitro with ()NO donor compounds. Using dihydrorhodamine 123 as a specific probe for ONOO(-) formation, a ratio of 100 microM dipropylenetriamine NONOate (DPTA/NO) to 10 microM 4-hydroxyestradiol (4-OHE(2)) gave an optimal ONOO(-) production of 11.9 +/- 1.9 microM (mean +/- SD). Quantification of ONOO(-) was not modified by mannitol, supporting the idea that the hydroxyl radical was not involved. This production of ONOO(-) required the presence of the catechol structure of estrogen metabolites since all methoxyestrogens that were tested were inactive. Hydroxyestrogen metabolites derived from estradiol showed the same efficiency in producing ONOO(-) as those originating from estrone. With DPTA/NO, the 4-hydroxyestrogens generated 30-40% more ONOO(-) than the 2-hydroxyestrogens. Optimal production of ONOO(-) was assessed with DPTA/NO and diethylenetriamine NONOate (initial ()NO generation rates of 0.76 and 0.08 microM min(-1), respectively). With faster ()NO-releasing compounds, such as diethylamine NONOate and spermine NONOate, lower levels of ONOO(-) were detected. These data suggest that once the optimal concentration of ()NO was obtained, the reaction between ()NO and 4-OHE(2) was saturated. The excess of ()NO would probably react with aqueous oxygen to form nitrite (NO(2)(-)). Since the third-order reaction rate for the reaction between 2()NO and O(2) is 2 x 10(6) M(-2) s(-1), it can therefore be suggested that the reaction between ()NO and 4-OHE(2) occurs at a faster rate.

摘要

在大多数(即便不是全部)乳腺癌肿瘤中,雌激素代谢都会发生改变。这些改变主要导致儿茶酚雌激素代谢物(2-羟基雌激素和4-羟基雌激素)的形成,它们可通过半醌/醌衍生物的氧化还原循环生成超氧阴离子自由基(O₂⁻·)。在乳腺癌细胞中,一氧化氮合酶的活性也常常升高,导致细胞暴露于一氧化氮(·NO)的水平增加。由于·NO能迅速与O₂⁻·反应生成过氧亚硝酸根阴离子(ONOO⁻),因此开展了本研究,以确定在体外将2-羟基雌激素和4-羟基雌激素与·NO供体化合物共同孵育时,是否会生成ONOO⁻。使用二氢罗丹明123作为检测ONOO⁻形成的特异性探针,100 μM的二丙三胺 NONO 酸盐(DPTA/NO)与10 μM的4-羟基雌二醇(4-OHE₂)的比例可使ONOO⁻的最佳生成量达到11.9±1.9 μM(平均值±标准差)。甘露醇对ONOO⁻的定量没有影响,这支持了羟基自由基未参与反应的观点。ONOO⁻的这种生成需要雌激素代谢物的儿茶酚结构存在,因为所有测试的甲氧基雌激素均无活性。源自雌二醇的羟基雌激素代谢物在生成ONOO⁻方面表现出与源自雌酮的代谢物相同的效率。使用DPTA/NO时,4-羟基雌激素生成的ONOO⁻比2-羟基雌激素多30%-40%。使用DPTA/NO和二乙三胺 NONO 酸盐(初始·NO生成速率分别为0.76和0.08 μM min⁻¹)评估了ONOO⁻的最佳生成情况。对于释放·NO速度更快的化合物,如二乙胺 NONO 酸盐和精胺 NONO 酸盐,检测到的ONOO⁻水平较低。这些数据表明,一旦获得最佳浓度的·NO,·NO与4-OHE₂之间的反应就会饱和。过量的·NO可能会与水中的氧气反应生成亚硝酸盐(NO₂⁻)。由于2·NO与O₂反应的三级反应速率为2×10⁶ M⁻² s⁻¹,因此可以认为·NO与4-OHE₂之间的反应速率更快。

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