神经保护
兴奋剂
敌手
受体
地唑西平
神经毒性
NMDA受体
受体拮抗剂
药理学
化学
Sigma-1受体
西格玛受体
生物
内科学
内分泌学
毒性
生物化学
医学
作者
Agostino Marrazzo,Filippo Caraci,Elisa Trovato Salinaro,Tsung‐Ping Su,Agata Copani,Giuseppe Ronsisvalle
出处
期刊:Neuroreport
[Ovid Technologies (Wolters Kluwer)]
日期:2005-07-13
卷期号:16 (11): 1223-1226
被引量:116
标识
DOI:10.1097/00001756-200508010-00018
摘要
Prolonged exposure of cultured cortical neurons to the residue 25-35 fragment of beta-amyloid protein, in the presence of dizocilpine, an antagonist of the N-methyl-D-aspartate receptor, and of 6,7-dinitroquinoxaline-2,3-dione, an antagonist of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate receptors, resulted in the expression of the proapoptotic protein Bax and neuronal death. Beta-amyloid protein(25-35)-induced neuronal death was substantially attenuated by the sigma1 receptor agonist 2-(4-morpholinethyl)1-phenylcyclohexanecarboxylate. The neuroprotective action of 2-(4-morpholinethyl)1-phenylcyclohexanecarboxylate was mimicked by the sigma1 ligand methyl (1S,2R)-2-[1-adamantyl(methyl)amino]methyl-1-phenylcyclopropanecarboxylate and was antagonized by the sigma1 receptor antagonist N,N-dipropyl-2-[4-methoxy-3-(2-phenylethoxy)-phenyl]-ethylamine monohydrochloride. These results suggest that sigma1 receptor agonists might function as neuroprotectant agents in Alzheimer's disease.
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