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

被引:22
作者
Antonova, Maria [1 ,2 ]
Wienecke, Troels [1 ,2 ]
Maubach, Karen [3 ]
Thomas, Emma [3 ]
Olesen, Jes [1 ,2 ]
Ashina, Messoud [1 ,2 ]
机构
[1] Univ Copenhagen, Danish Headache Ctr, DK-2600 Glostrup, Denmark
[2] Univ Copenhagen, Dept Neurol, Fac Hlth Sci, Glostrup Hosp, DK-2600 Glostrup, Denmark
[3] BTG, London EC4M 7RD, England
关键词
Prostaglandin E-2; EP4 receptor antagonist; BGC20-1531; Vasodilatation; Headache; CEREBRAL-ARTERIES; CARBOXYL-TERMINUS; IN-SITU; SUBTYPE; MIGRAINE; AGONIST; CAMP; DESENSITIZATION; CLASSIFICATION; SENSITIZATION;
D O I
10.1007/s10194-011-0358-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Using a human Prostaglandin E-2 (PGE(2)) 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 PGE(2). 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 PGE(2) induced headache and dilatation in normal subjects.
引用
收藏
页码:551 / 559
页数:9
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