Characterization of LY344864 as a pharmacological tool to study 5-HT1F receptors: Binding affinities, brain penetration and activity in the neurogenic dural inflammation model of migraine

被引：107

作者：

Phebus, LA ^{[1
]}

Johnson, KW ^{[1
]}

Zgombick, JM ^{[1
]}

Gilbert, PJ ^{[1
]}

VanBelle, K ^{[1
]}

Mancuso, V ^{[1
]}

Nelson, DLG ^{[1
]}

Calligaro, DO ^{[1
]}

Kiefer, AD ^{[1
]}

Branchek, TA ^{[1
]}

Flaugh, ME ^{[1
]}

机构：

[1] SYNAPT PHARMACEUT CORP,PARAMUS,NJ 07652

来源：

LIFE SCIENCES | 1997年 / 61卷 / 21期

关键词：

LY344864; migraine; neurogenic dural inflammation;

D O I：

10.1016/S0024-3205(97)00885-0

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：

LY344864 is a selective receptor agonist with an affinity of 6 nM (K-i) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined. When examined for its ability to inhibit forskolin-induced cyclic AMP accumulation in cells stably transfected with human 5-HT1F receptors, LY344864 was shown to be a full agonist producing an effect similar in magnitude to serotonin itself. After an intravenous dose of 1 mg/kg, rat plasma LY344864 levels declined with time whereas brain cortex levels remained relatively constant for the first 6 hours after injection. Oral and intravenous LY344864 administration potently inhibited dural protein extravasation caused by electrical stimulation of the trigeminal ganglion in rats. Taken together, these data demonstrate that LY344864 is a selective 5-HT1F receptor agonist that can be used to explore both the in vitro and in vivo functions of this receptor.

引用

页码：2117 / 2126

页数：10

共 22 条

[11] 5-HT1F receptor agonists inhibit neurogenic dural inflammation in guinea pigs [J].