首页> 美国卫生研究院文献>The Journal of Headache and Pain >The pharmacological effect of BGC20-1531 a novel prostanoid EP4 receptor antagonist in the Prostaglandin E2 human model of headache
【2h】

The pharmacological effect of BGC20-1531 a novel prostanoid EP4 receptor antagonist in the Prostaglandin E2 human model of headache

机译:新型前列腺素EP4受体拮抗剂BGC20-1531在前列腺素E2头痛人类模型中的药理作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Using a human Prostaglandin E2 (PGE2) model of headache, we examined whether a novel potent and selective EP4 receptor antagonist, BGC20-1531, may prevent headache and dilatation of the middle cerebral (MCA) and superficial temporal artery (STA). In a three-way cross-over trial, eight healthy volunteers were randomly allocated to receive 200 and 400 mg BGC20-1531 and placebo, followed by a 25-min infusion of PGE2. We recorded headache intensity on a verbal rating scale, MCA blood flow velocity and STA diameter. There was no difference in headache response or prevention of the dilation of the MCA or the STA (P > 0.05) with either dose of BGC20-1531 relative to placebo, although putative therapeutic exposures were not reached in all volunteers. In conclusion, these data suggest that the other EP receptors may be involved in PGE2 induced headache and dilatation in normal subjects.
机译:使用人类前列腺素E2(PGE2)头痛模型,我们检查了新型有效且选择性的EP4受体拮抗剂BGC20-1531是否可以预防中脑(MCA)和颞浅动脉(STA)的头痛和扩张。在一项三项交叉试验中,随机分配了八名健康志愿者接受200和400 mg BGC20-1531和安慰剂,然后输注PGE2 25分钟。我们以语言评定量表,MCA血流速度和STA直径记录头痛强度。 BGC20-1531的任一剂量与安慰剂相比,头痛反应或预防MCA或STA扩张均无差异(P> 0.05),尽管并未在所有志愿者中达到假定的治疗暴露水平。总之,这些数据表明其他EP受体可能与正常受试者中PGE2引起的头痛和扩张有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号