Inhibition of Human Monoamine Oxidase: Biological and Molecular Modeling Studies on Selected Natural Flavonoids

被引:88
作者
Carradori, Simone [1 ]
Gidaro, Maria Concetta [2 ]
Petzer, Anel [3 ]
Costa, Giosue [2 ]
Guglielmi, Paolo [4 ]
Chimenti, Paola [4 ]
Alcaro, Stefano [2 ]
Petzer, Jacobus P. [3 ]
机构
[1] G dAnnunzio Univ Chieti Pescara, Dept Pharm, Via Vestini 31, I-66100 Chieti, Italy
[2] Magna Graecia Univ Catanzaro, Dipartimento Sci Salute, Campus Univ S Venuta,Viale Europa Loc Germaneto, I-88100 Catanzaro, Italy
[3] North West Univ, Ctr Excellence Pharmaceut Sci, ZA-2531 Potchefstroom, South Africa
[4] Sapienza Univ Rome, Dept Drug Chem & Technol, Ple A Moro 5, I-00185 Rome, Italy
关键词
monoamine oxidase inhibitor; apigenin; taxifolin; diosmetin; naringin; eriocitrin; isorhamnetin; hesperidin; quercetin-3-O-glucoside; HUMAN MAO-A; HIGH-POTENCY; QUERCETIN; CAFFEINE; DESIGN;
D O I
10.1021/acs.jafc.6b03529
中图分类号
S [农业科学];
学科分类号
082806 [农业信息与电气工程];
摘要
Naturally occurring flavonoids display a plethora of different biological activities, but emerging evidence suggests that this class of compounds may also act as antidepressant agents endowed with multiple mechanisms of action in the central nervous system, increasing central neurotransmission, limiting the reabsorption of bioamines by synaptosomes, and modulating the neuroendocrine and GABA(A) systems. Due to their presence in foods, food-derived products, and nutraceuticals, we established their role and structure-activity relationships as reversible and competitive human monoamine oxidase (MAO) inhibitors. In addition, molecular modeling studies, which evaluated their modes of MAO inhibition, are presented. These findings could provide pivotal implications in the quest of novel drug-like compounds and for the establishment of harmful drug-dietary supplement interactions commonly reported in the therapy with antidepressant agents.
引用
收藏
页码:9004 / 9011
页数:8
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