EMD 68843, a serotonin reuptake inhibitor with selective presynaptic 5-HT1A receptor agonistic properties

被引:70
作者
Bartoszyk, GD
Hegenbart, R
Ziegler, H
机构
[1] Merck KGaA, Department of CNS-Research, CNS-Pharmacology
关键词
5-HT1A autoreceptor; EMD; 68843; 8-OH-DPAT (8-hydroxy-2-(di-n-propylamino)tetralin); fluoxetine; WAY; 100635; hypothermia; ultrasonic vocalization; (rat);
D O I
10.1016/S0014-2999(96)00999-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The 5-HT1A receptor agonist 8-hydroxy-(di-n-propylamino)tetralin (8-OH-DPAT; 0.55 mg/kg s.c.) and the 5-HT (5-hydroxytryptamine, serotonin) reuptake inhibitor/5-HT1A receptor ligand 5-{4-[4-(5-cyano-3-indolyl)-butyl]-1-piperazinyl}-benzofuran-2-carboxamide (EMD 68843; 55 mg/kg p.o.) inhibited ultrasonic vocalization in rats, an effect which was antagonized by the 5-HT1A receptor antagonist N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]-ethyl]-N-(2-pyridyl)-cyclohexancarboxamide(WAY 100635; 1.0 mg/kg s.c.). 8-OH-DPAT decreased body temperature in rats, an effect which was also antagonized by WAY 100635, whereas EMD 68843 neither affected body temperature by itself nor interacted with 8-OH-DPAT or WAY 100635. The selective 5-HT reuptake inhibitor fluoxetine (100 mg/kg p.o.) had no effect on ultrasonic vocalization or body temperature. Therefore EMD 68843 is suggested to be a 5-HT1A receptor agonist selective for presynaptic 5-HT1A receptors. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:147 / 153
页数:7
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