MIXED AGONIST ANTAGONIST PROPERTIES OF NAN-190 AT 5-HT1A RECEPTORS - BEHAVIORAL AND INVIVO BRAIN MICRODIALYSIS STUDIES

被引:145
作者
HJORTH, S
SHARP, T
机构
[1] UNIV OXFORD, RADCLIFFE INFIRM, MRC UNIT, OXFORD OX2 6HE, ENGLAND
[2] UNIV OXFORD, RADCLIFFE INFIRM, DEPT CLIN, OXFORD OX2 6HE, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0024-3205(90)90097-B
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
1-(2-Methoxyphenyl)-4-[4-(2-phthalimido)butyl]piperazine, NAN-190, is a novel compound with putative 5-HT1A antagonist properties. In the present study, the effects of NAN-190 were examined with regard to functional pre- and postsynaptic 5-HT1A receptor-mediated events, using in vivo brain microdialysis and behavioural techniques. Our findings provide evidence that NAN-190 acts as a mixed agonist/antagonist at central 5-HT1A receptors. Thus, NAN-190 blocked (+)8-OH-DPAT-induced behaviour in reserpinized rats, indicating antagonist properties at postsynaptic 5-HT1A receptors. However, the compound was also able to decrease the release of 5-HT in vivo, tentatively due to an agonist action at somatodendritic 5-HT1A autoreceptors. These data extend previous information on the pharmacological profile of NAN-190 and further emphasizes the difference between pre- and postsynaptic 5-HT1A receptors in brain. © 1990.
引用
收藏
页码:955 / 963
页数:9
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