Paladini A C, Marder M, Viola H, Wolfman C, Wasowski C, Medina J H
Instituto de Quimica y Fisicoquimica Biologicas, Facultad de Farmacia y Bioquimica, Buenos Aires, Argentina.
J Pharm Pharmacol. 1999 May;51(5):519-26. doi: 10.1211/0022357991772790.
The list of activities of plant flavonoids did not include effects on the central nervous system (CNS) up to 1990, when our laboratory described the existence of natural anxiolytic flavonoids. The first of these was chrysin (5,7-dihydroxyflavone), followed by apigenin (5,7,4'-trihydroxyflavone) and flavone itself. Semisynthetic derivatives of flavone obtained by introducing halogens, nitro groups or both in its molecule, give rise to high affinity ligands for the benzodiazepine receptor, active in-vivo; 6,3'-dinitroflavone, for example, is an anxiolytic drug 30 times more potent than diazepam. The data collected in this paper make clear that some natural flavonoids are CNS-active molecules and that the chemical modification of the flavone nucleus dramatically increases their anxiolytic potency.
直到1990年,植物黄酮类化合物的活性列表中都没有对中枢神经系统(CNS)的影响,当时我们实验室描述了天然抗焦虑黄酮类化合物的存在。其中第一种是白杨素(5,7 - 二羟基黄酮),其次是芹菜素(5,7,4'-三羟基黄酮)和黄酮本身。通过在黄酮分子中引入卤素、硝基或两者而获得的半合成衍生物,产生了对苯二氮䓬受体具有高亲和力的配体,在体内具有活性;例如,6,3'-二硝基黄酮是一种抗焦虑药物,其效力比地西泮强30倍。本文收集的数据表明,一些天然黄酮类化合物是中枢神经系统活性分子,并且黄酮核的化学修饰显著提高了它们的抗焦虑效力。