Contractile responses to sumatriptan and ergotamine in the rabbit saphenous vein:: effect of selective 5-HT1F receptor agonists and PGF2α

被引:28
作者
Cohen, ML [1 ]
Schenck, K [1 ]
机构
[1] Eli Lilly & Co, Lilly Corp Ctr, Indianapolis, IN 46285 USA
关键词
rabbit saphenous vein; ergotamine; sumatriptan; contraction; PGF(2 alpha) augmented contraction; 5-HT1F receptor agonists;
D O I
10.1038/sj.bjp.0703587
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Contractile responses to ergotamine. sumatriptan and the novel 5-HT1F receptor agonists LY334370 and LY334864 were examined using the rabbit saphenous vein. 2 Ergotamine (pEC(50) = 8.7 +/- 0.06) was 30 fold more potent than 5-hydroxytryptamine (5-HT) (pEC(50) = 7.2 +/- 0.13) and 300 fold more potent than sumatriptan (pEC(50) = 6.0 +/- 0.08) in contracting the rabbit saphenous vein in vitro. The selective 5-HT1F receptor agonists, LY334370 or LY344864 (up to 10(-4) M). did not contract the rabbit saphenous vein. 3 The contractile response to ergotamine in this tissue resulted from activation of both alpha, and 5-HT1B1D receptors based on the observation that prazosin (10(-6) M), an alpha-adrenoceptor antagonist, and GR127935 (10(-8) M) a 5-HT1B1D receptor antagonist, dextrally shifted the contractile response to ergotamine. In contrast, prazosin (10(-6) M) did not alter contraction to sumatriptan whereas GR127935 (10(-8) M) was a potent antagonist (-log K-B = 10.0) suggesting that sumatriptan-induced contraction of the rabbit saphenous vein was mediated only by activation of receptors similar or identical to 5-HT1B1D receptors. 4 PGF(2 alpha) (3 x 10(-7) M) produced a modest increase (approximately 5.0-10.0% maximum PGF(2 alpha) contraction! In saphenous vein force. Precontraction with PGF(2 alpha) (3 x 10(-7) M) dramatically augmented the potency and maximal contractile response to sumatriptan (pEC(50) = 7.1) and modestly enhanced the contractile potency of ergotamine (pEC(50) = 9.0) in the rabbit saphenous vein. However. PGF(2 alpha) (3 x 10(-7) M) only unmasked a contraction to the 5-HT1F receptor agonists when concentrations exceeded 10(-5) M. concentrations considerably higher than their 5-HT1F receptor affinities. 5 LY334370(10(-6) M) pretreatment did not alter contraction to either sumatriptan or ergotamine aod a higher concentration (10(-5) M) of LY334370 or LY344864 inhibited contraction to sumatriptan. 6 Thus, activation of 5-HT1F receptors will not induce vascular contraction (either alone or following modest tone with PGF(2 alpha)) or augment contraction to other contractile agonists in the rabbit saphenous vein.
引用
收藏
页码:562 / 568
页数:7
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