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依来曲普坦(UK-116,044)的体内药理学特征:一种强效新型5-HT(1B/1D)受体激动剂。

The in vivo pharmacological profile of eletriptan (UK-116,044): a potent and novel 5-HT(1B/1D) receptor agonist.

作者信息

Gupta P, Butler P, Shepperson N B, McHarg A

机构信息

Department of Discovery Biology, Pfizer Central Research, Sandwich, CT13 9NJ, Kent, UK.

出版信息

Eur J Pharmacol. 2000 Jun 9;398(1):73-81. doi: 10.1016/s0014-2999(00)00240-5.

Abstract

The anti-migraine drug, eletriptan [(R)-3-(1-methyl-2-pyrrolidinylmethyl)-5-[2-(phenylsulphonyl )ethyl]-1 H-indole; UK-116,044], is a novel 5-HT(1B/1D) receptor agonist. In this paper, the regional vasoconstrictor profile of eletriptan, in comparison with sumatriptan, was examined in the anaesthetised dog. The inhibitory actions of eletriptan on neurogenic inflammation in rat dura mater were also assessed. In the anaesthetised dog, eletriptan (1-1000 microg kg(-1) i.v.) produced a dose-dependent reduction of carotid arterial blood flow with a similar potency and maximum effect to sumatriptan (ED(50) values: eletriptan and sumatriptan, 12 and 9 microg kg(-1), i.v., respectively). However, eletriptan exhibited a significantly lower potency than sumatriptan in reducing coronary artery diameter (ED(50) values: 63 and 19 microg kg(-1), i.v., respectively, P<0.05). In the femoral circulation, sumatriptan caused a significant reduction in arterial blood flow (ED(50) 35 microg kg(-1) i.v.) whereas eletriptan (1-1000 microg kg(-1) i.v.) had no significant effect upon femoral arterial blood flow when compared to vehicle-treated animals. In rats, eletriptan (30-300 microg kg(-1) i.v.) administered prior to electrical stimulation of the trigeminal ganglion produced a dose-related and complete inhibition of plasma protein extravasation in the dura mater (mean extravasation ratio: control 1.9; eletriptan 1.0, minimum effective dose 100 microg kg(-1), P<0.05). The potency and maximum effect of eletriptan was identical to that of sumatriptan in this model. When administered during a period of continual stimulation of the trigeminal nerve, eletriptan (100 microg kg(-1) i.v.) produced a complete inhibition of plasma protein extravasation. The ability to reduce canine carotid arterial blood flow and inhibit neurogenic inflammation in rat dura mater suggests that vascular and neurogenic mechanisms may contribute to eletriptan's clinical efficacy in migraine patients. In addition, eletriptan exhibits some selectivity for reducing carotid arterial blood flow when compared with femoral arterial blood flow and coronary artery diameter, in the anaesthetised dog.

摘要

抗偏头痛药物依立曲坦[(R)-3-(1-甲基-2-吡咯烷基甲基)-5-[2-(苯磺酰基)乙基]-1H-吲哚;UK-116,044]是一种新型的5-HT(1B/1D)受体激动剂。本文在麻醉犬中研究了依立曲坦与舒马曲坦相比的局部血管收缩情况。还评估了依立曲坦对大鼠硬脑膜神经源性炎症的抑制作用。在麻醉犬中,依立曲坦(1 - 1000微克·千克⁻¹静脉注射)使颈动脉血流量呈剂量依赖性减少,其效力和最大效应与舒马曲坦相似(半数有效剂量值:依立曲坦和舒马曲坦分别为12和9微克·千克⁻¹静脉注射)。然而,在减少冠状动脉直径方面,依立曲坦的效力显著低于舒马曲坦(半数有效剂量值:分别为63和19微克·千克⁻¹静脉注射,P<0.05)。在股循环中,舒马曲坦使动脉血流量显著减少(半数有效剂量35微克·千克⁻¹静脉注射),而与给予赋形剂处理的动物相比,依立曲坦(1 - 1000微克·千克⁻¹静脉注射)对股动脉血流量无显著影响。在大鼠中,在电刺激三叉神经节之前静脉注射依立曲坦(30 - 300微克·千克⁻¹)可使硬脑膜血浆蛋白外渗产生剂量相关的完全抑制(平均外渗率:对照组1.9;依立曲坦1.0,最小有效剂量100微克·千克⁻¹,P<0.05)。在该模型中,依立曲坦的效力和最大效应与舒马曲坦相同。当在持续刺激三叉神经期间给药时,依立曲坦(100微克·千克⁻¹静脉注射)可使血浆蛋白外渗完全抑制。依立曲坦减少犬颈动脉血流量和抑制大鼠硬脑膜神经源性炎症的能力表明,血管和神经源性机制可能有助于依立曲坦对偏头痛患者的临床疗效。此外,在麻醉犬中,与股动脉血流量和冠状动脉直径相比,依立曲坦在减少颈动脉血流量方面表现出一定的选择性。

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