嗜中性
药理学
拉莫三嗪
抗惊厥药
抗抑郁药
苯妥英钠
敌手
作用机理
癫痫
化学
医学
神经科学
心理学
海马体
受体
生物化学
体外
出处
期刊:PubMed
日期:2002-11-01
卷期号:60 (6): 415-22
被引量:10
摘要
Pharmacological studies on tetrahydro-N, N-dimethyl-5, 5-diphenyl-3-furanemethanamine (AE14) pointed out its prominent action in the passive avoidance test, its antagonist effect on electrogenic (maximal electroshock, MES) or pentetrazole-induced tonic convulsions, and its anti-immobility effect in the forced swim test (FST) in mice. These pharmacological data suggest that AE14 could exhibit nootropic, antiepileptic and antidepressant actions. Molecular pharmacology studies (receptology, bioresponse) with AE14 showed a selective M1 muscarinic agonism, one of the most potent currently known, and an affinity for site 2 of the sodium ion channels, at least as strong as those of first or second generation antiepileptics (phenytoin, lamotrigine). These molecular effects show that AE14 could be a potential second generation anti-Alzheimer drug, a third generation antiepileptic, and an adjunct for antidepressants.
科研通智能强力驱动
Strongly Powered by AbleSci AI