Donepezil, But Not Galantamine, Blocks Muscarinic Receptor-Mediated In Vitro and In Vivo Responses

被引:13
作者
Ago, Yukio [1 ]
Koda, Ken [1 ]
Ota, Yuki [1 ]
Kita, Yuki [1 ]
Fukada, Asako [1 ]
Takuma, Kazuhiro [1 ]
Matsuda, Toshio [1 ,2 ,3 ]
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Lab Med Pharmacol, Osaka 565871, Japan
[2] Kanazawa Univ, Osaka Univ, United Grad Sch Child Dev, Osaka 565871, Japan
[3] Osaka Univ, Hamamatsu Univ Sch Med, Osaka 565871, Japan
基金
日本学术振兴会;
关键词
donepezil; galantamine; muscarinic receptor; Ca2+; DA release; SH-SY5Y cell; mouse cerebral cortex; PREPULSE INHIBITION; N-DESMETHYLCLOZAPINE; INDUCED DEFICITS; DOPAMINE; ACETYLCHOLINE; MODULATION; CLOZAPINE;
D O I
10.1002/syn.20969
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have found that galantamine, but not donepezil, reversed isolation rearing-induced deficits of prepulse inhibition (PPI) via an activation of muscarinic M1 receptors. To explain this difference, the present study examined the effects of these acetylcholinesterase inhibitors on muscarinic receptor-mediated responses in in vitro and in vivo systems. Ca2+-imaging study showed that donepezil, but not galantamine, blocked a muscarinic agonist carbachol-induced increase in intracellular Ca2+ levels in SH-SY5Y cells. Moreover, a microdialysis study showed that intraperitoneal administration of donepezil, but not galantamine, attenuated a preferential M1 receptor agonist Ndesmethylclozapine-induced increase in dopamine release in mouse cerebral cortex. These results suggest that donepezil, but not galantamine, has an ability to block muscarinic receptor function and imply that the differential effects may be responsible for the difference in the effects on isolation rearing-induced deficits of PPI between these drugs. Synapse 65:1373-1377, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1373 / 1377
页数:5
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