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大环铜(II)配合物:超氧化物清除活性、结构研究及细胞毒性评估。

Macrocyclic copper(II) complexes: superoxide scavenging activity, structural studies and cytotoxicity evaluation.

作者信息

Fernandes Ana S, Gaspar Jorge, Cabral M Fátima, Caneiras Cátia, Guedes Rita, Rueff José, Castro Matilde, Costa Judite, Oliveira Nuno G

机构信息

CECF, Faculty of Pharmacy, University of Lisbon, Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.

出版信息

J Inorg Biochem. 2007 May;101(5):849-58. doi: 10.1016/j.jinorgbio.2007.01.013. Epub 2007 Feb 11.

Abstract

Synthetic superoxide dismutase mimetics have emerged as a potential novel class of drugs for the treatment of oxidative stress related diseases. Among these agents, metal complexes with macrocyclic ligands constitute an important group. In this work we synthesized five macrocyclic copper(II) complexes and evaluated their ability to scavenge the superoxide anions generated by the xanthine-xanthine oxidase system. Two different endpoints were used, the nitro blue tetrazolium (NBT) reduction assay (colorimetric method) and the dihydroethidium (DHE) oxidation assay (fluorimetric method). IC(50) values in the low micromolar range were found in four out of five macrocyclic complexes studied, demonstrating their effective ability to scavenge the superoxide anion. The IC(50) values obtained with the NBT assay for the macrocyclic copper(II) complexes, were consistently higher, approximately threefold, than those obtained with the DHE assay. Spectroscopic and electrochemical studies were performed in order to correlate the structural features of the complexes with their superoxide scavenger activity. Cytotoxicity assays were also performed using the MTT method in V79 mammalian cells and we found that the complexes, in the range of concentrations tested in the superoxide scavenging assays were not considerably toxic. In summary, some of the presented macrocyclic copper(II) complexes, specially those with a high stability constant and low IC(50), appear to be promising superoxide scavenger agents, and should be considered for further biological assays.

摘要

合成超氧化物歧化酶模拟物已成为一类潜在的新型药物,用于治疗与氧化应激相关的疾病。在这些药物中,含有大环配体的金属配合物是一个重要的类别。在这项工作中,我们合成了五种大环铜(II)配合物,并评估了它们清除黄嘌呤 - 黄嘌呤氧化酶系统产生的超氧阴离子的能力。使用了两种不同的终点方法,即硝基蓝四唑(NBT)还原测定法(比色法)和二氢乙锭(DHE)氧化测定法(荧光法)。在所研究的五种大环配合物中,有四种的半数抑制浓度(IC50)值处于低微摩尔范围内,表明它们具有清除超氧阴离子的有效能力。用NBT测定法获得的大环铜(II)配合物的IC50值始终高于用DHE测定法获得的值,约为其三倍。进行了光谱和电化学研究,以便将配合物的结构特征与其超氧清除剂活性相关联。还使用MTT法在V79哺乳动物细胞中进行了细胞毒性测定,我们发现在超氧清除测定中测试的浓度范围内,这些配合物没有明显的毒性。总之,本文提出的一些大环铜(II)配合物,特别是那些具有高稳定性常数和低IC50的配合物,似乎是有前途的超氧清除剂,应考虑进行进一步的生物学测定。

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