Epileptic Targets and Drugs: A Mini-Review

被引:4
|
作者
Rodrigues, Teresa Carolliny Moreira Lustoza [1 ]
de Moura, Jessica Paiva [1 ]
dos Santos, Aline Matilde Ferreira [1 ]
Monteiro, Alex France M. [1 ]
Lopes, Simone Mendes [1 ]
Scotti, Marcus Tullius [1 ]
Scotti, Luciana [1 ,2 ]
机构
[1] Univ Fed Paraiba, Hlth Sci Ctr, BR-50670910 Joao Pessoa, PB, Brazil
[2] Univ Fed Paraiba, Univ Hosp, Teaching & Res Management, Joao Pessoa, PB, Brazil
关键词
Molecular docking; AMPA; NMDA; GAT1; KCNQ; Cav; Nav e GABAA; SODIUM-CHANNEL; ANXIOLYTIC-LIKE; ANTICONVULSANT; DERIVATIVES; DESIGN; INHIBITORS; PHYSIOLOGY; RECEPTORS; MECHANISM; ACID;
D O I
10.2174/1389450123666220927103715
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Epilepsy is a neurological disease affected by an imbalance of inhibitory and excitatory signaling in the brain. Introduction: In this disease, the targets are active in pathophysiology and thus can be used as a focus for pharmacological treatment. Methods: Several studies demonstrated the antiepileptic effect of drugs acting on the following targets: N-methyl-D-aspartate (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor, voltage-gated calcium channel (Cav), Gamma aminobutyric acid transporter type 1 (GAT1), voltage-gated sodium channels (Nav), voltage-gated potassium channel of the Q subfamily (KCNQ) and Gamma aminobutyric acid type A (GABAA) receiver. Results: These studies highlight the importance of molecular docking. Conclusion: Quantitative Structure-Activity Relationship (QSAR) and computer aided drug design (CADD) in predicting of possible pharmacological activities of these targets.
引用
收藏
页码:212 / 224
页数:13
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