Wada K, Fujibayashi Y, Yokoyama A
Department of Radiopharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.
Arch Biochem Biophys. 1994 Apr;310(1):1-5. doi: 10.1006/abbi.1994.1132.
To obtain a superoxide dismutase (SOD)-like drug that could readily cross the cell membrane, we investigated the SOD-like activity, intracellular uptake, and stability of several Cu(II)Bisthiosemicarbazones (Cu(II)BTS). Among these Cu(II)BTS chelates, Cu(II)[2,3-Butanedionebis(N4-methylthiosemicarbazone)] (Cu(II)BMTS) was the most effective SOD-like compound with activity similar to activity reported for various previously reported SOD-like Cu complexes. Biodistribution studies in mice indicated that Cu(II)BMTS rapidly distributed to all tissues and readily crossed cell membranes as well as the blood-brain barrier with high distributions to the brain and the heart. Moreover, Cu(II)BMTS was stable in mouse brain homogenate and mouse blood. These results suggest that Cu(II)BMTS has the potential to be used as a SOD-like drug capable of reaching intracellular superoxide generating sites.
为了获得一种能够轻易穿过细胞膜的超氧化物歧化酶(SOD)样药物,我们研究了几种双硫代半卡巴腙铜(II)(Cu(II)BTS)的SOD样活性、细胞内摄取和稳定性。在这些Cu(II)BTS螯合物中,Cu(II)[2,3-丁二酮双(N4-甲基硫代半卡巴腙)](Cu(II)BMTS)是最有效的SOD样化合物,其活性与先前报道的各种SOD样铜配合物的活性相似。在小鼠体内的生物分布研究表明,Cu(II)BMTS迅速分布到所有组织,并能轻易穿过细胞膜以及血脑屏障,在脑和心脏中有较高的分布。此外,Cu(II)BMTS在小鼠脑匀浆和小鼠血液中稳定。这些结果表明,Cu(II)BMTS有潜力用作一种能够到达细胞内超氧化物产生部位的SOD样药物。