Inhibition of brain mitochondrial monoamine oxidases by the endogenous compound 5-hydroxyoxindole

被引:16
作者
Crumeyrolle-Arias, M [1 ]
Tournaire, MC
Cane, A
Launay, JM
Barritault, D
Medvedev, A
机构
[1] Univ Paris 12, Lab CRRET, CNRS, FRE 2412, F-94010 Creteil, France
[2] Hop Lariboisiere, Serv Biochim, SFR 6, F-75006 Paris, France
[3] Russian Acad Med Sci, Inst Biomed Chem, Moscow, Russia
基金
俄罗斯基础研究基金会;
关键词
brain MAO; 5-hydroxyoxindole; isatin; endogenous regulation; oxidized indoles;
D O I
10.1016/j.bcp.2003.10.021
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
5-Hydroxyoxindole is a recently identified endogenous compound. Its physiological role remains unclear but certain evidence exists, that it may share some regulatory properties with isatin, a known endogenous inhibitor of monoamine oxidase (MAO) type B (MAO-B). In this study several oxidized indoles were tested for their in. vitro inhibition of MAO type A (MAO-A) and B of rat brain non-synaptic mitochondria. 5-Hydroxyoxindole was less potent MAO-A inhibitor (IC50 56.8 muM) than isatin (31.8 muM) and especially 5-hydroxyisatin (6.5 muM), but it was the only highly selective MAO-A inhibitor among the all compounds studied (IC50 MAO-A:IC50 MAO-B = 0.044). Thus, the in vitro data suggest that MAO-A may represent potential target for 5-hydroxyoxindole. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:977 / 979
页数:3
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