Neuroactive flavonoids: new ligands for the Benzodiazepine receptors

被引:75
作者
Medina, JH
Viola, H
Wolfman, C
Marder, M
Wasowski, C
Calvo, D
Paladini, AC
机构
[1] Univ Buenos Aires, Fac Farm & Bioquim, Inst Quim & Fisioquim Biol, CONICET, RA-1113 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Fac Med, Inst Biol Celular & Neurociencias, Buenos Aires, DF, Argentina
关键词
flavonoids; anxiolysis; benzodiazepine receptors; partial agonist;
D O I
10.1016/S0944-7113(98)80034-2
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Flavonoids isolated from plants used as tranquilizers in folkloric medicine have a selective affinity, for central benzodiazepine receptors (BDZ-Rs) and some of them possess a pharmacological profile compatible with a partial agonist action. Synthetic derivatives of the common flavone nucleus, give rise to high affinity ligands when electronegative groups are introduced in carbons 6 and/or 3'. Representative compounds such as 6,3'-dinitroflavone and, 6-bromo-3'-nitroflavone exhibit a high affinity for the BDZ-Rs (Ki = 1.5 to 30 nM) and have anxiolytic effects not associated with myorelaxant, sedative or amnesic actions. These compounds or similar ones, could lead to improved therapeutic drugs in the treatment of anxiety.
引用
收藏
页码:235 / 243
页数:9
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