CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine

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Standard

CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine. / Tvedskov, J F; Tfelt-Hansen, P; Petersen, K A; Jensen, Lars Thorbjørn; Olesen, J.

I: Cephalalgia : an international journal of headache, Bind 30, Nr. 11, 11.2010, s. 1346-53.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Tvedskov, JF, Tfelt-Hansen, P, Petersen, KA, Jensen, LT & Olesen, J 2010, 'CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine', Cephalalgia : an international journal of headache, bind 30, nr. 11, s. 1346-53. https://doi.org/10.1177/0333102410363491

APA

Tvedskov, J. F., Tfelt-Hansen, P., Petersen, K. A., Jensen, L. T., & Olesen, J. (2010). CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine. Cephalalgia : an international journal of headache, 30(11), 1346-53. https://doi.org/10.1177/0333102410363491

Vancouver

Tvedskov JF, Tfelt-Hansen P, Petersen KA, Jensen LT, Olesen J. CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine. Cephalalgia : an international journal of headache. 2010 nov.;30(11):1346-53. https://doi.org/10.1177/0333102410363491

Author

Tvedskov, J F ; Tfelt-Hansen, P ; Petersen, K A ; Jensen, Lars Thorbjørn ; Olesen, J. / CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine. I: Cephalalgia : an international journal of headache. 2010 ; Bind 30, Nr. 11. s. 1346-53.

Bibtex

@article{f46b0092617c4b0eb52971a56767845d,
title = "CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine",
abstract = "UNLABELLED: There is a striking similarity between the migraine-provoking effect of the nitric oxide (NO) donor glyceryl trinitrate (GTN) and that of calcitonin gene-related peptide (CGRP). We tested the hypothesis that NO releases CGRP to cause the delayed migraine attack after GTN.METHODS: In a double-blind-cross-over study, 13 migraine without aura (MO) patients were administered GTN 0.5 µg/kg/minute for 20 minutes and subsequently BIBN4096BS (olcegepant) 10 mg or placebo. Headache scores and development of MO were followed for 24 hours.RESULTS: MO developed in seven of 13 with olcegepant and in nine of 13 with placebo (p=0.68). The headache scores were similar after the two treatments (p=0.58). Thus CGRP receptor blockade did not prevent GTN-induced migraine.CONCLUSIONS: The present study indicates that NO does not induce migraine by liberating CGRP. The most likely explanation for our findings is that CGRP has its effect higher than NO in the cascade of events leading to MO attacks.",
keywords = "Adult, Cross-Over Studies, Dipeptides, Double-Blind Method, Female, Humans, Male, Middle Aged, Migraine Disorders, Nitroglycerin, Quinazolines, Receptors, Calcitonin Gene-Related Peptide, Vasodilator Agents, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't",
author = "Tvedskov, {J F} and P Tfelt-Hansen and Petersen, {K A} and Jensen, {Lars Thorbj{\o}rn} and J Olesen",
year = "2010",
month = nov,
doi = "10.1177/0333102410363491",
language = "English",
volume = "30",
pages = "1346--53",
journal = "Cephalalgia",
issn = "0800-1952",
publisher = "SAGE Publications",
number = "11",

}

RIS

TY - JOUR

T1 - CGRP receptor antagonist olcegepant (BIBN4096BS) does not prevent glyceryl trinitrate-induced migraine

AU - Tvedskov, J F

AU - Tfelt-Hansen, P

AU - Petersen, K A

AU - Jensen, Lars Thorbjørn

AU - Olesen, J

PY - 2010/11

Y1 - 2010/11

N2 - UNLABELLED: There is a striking similarity between the migraine-provoking effect of the nitric oxide (NO) donor glyceryl trinitrate (GTN) and that of calcitonin gene-related peptide (CGRP). We tested the hypothesis that NO releases CGRP to cause the delayed migraine attack after GTN.METHODS: In a double-blind-cross-over study, 13 migraine without aura (MO) patients were administered GTN 0.5 µg/kg/minute for 20 minutes and subsequently BIBN4096BS (olcegepant) 10 mg or placebo. Headache scores and development of MO were followed for 24 hours.RESULTS: MO developed in seven of 13 with olcegepant and in nine of 13 with placebo (p=0.68). The headache scores were similar after the two treatments (p=0.58). Thus CGRP receptor blockade did not prevent GTN-induced migraine.CONCLUSIONS: The present study indicates that NO does not induce migraine by liberating CGRP. The most likely explanation for our findings is that CGRP has its effect higher than NO in the cascade of events leading to MO attacks.

AB - UNLABELLED: There is a striking similarity between the migraine-provoking effect of the nitric oxide (NO) donor glyceryl trinitrate (GTN) and that of calcitonin gene-related peptide (CGRP). We tested the hypothesis that NO releases CGRP to cause the delayed migraine attack after GTN.METHODS: In a double-blind-cross-over study, 13 migraine without aura (MO) patients were administered GTN 0.5 µg/kg/minute for 20 minutes and subsequently BIBN4096BS (olcegepant) 10 mg or placebo. Headache scores and development of MO were followed for 24 hours.RESULTS: MO developed in seven of 13 with olcegepant and in nine of 13 with placebo (p=0.68). The headache scores were similar after the two treatments (p=0.58). Thus CGRP receptor blockade did not prevent GTN-induced migraine.CONCLUSIONS: The present study indicates that NO does not induce migraine by liberating CGRP. The most likely explanation for our findings is that CGRP has its effect higher than NO in the cascade of events leading to MO attacks.

KW - Adult

KW - Cross-Over Studies

KW - Dipeptides

KW - Double-Blind Method

KW - Female

KW - Humans

KW - Male

KW - Middle Aged

KW - Migraine Disorders

KW - Nitroglycerin

KW - Quinazolines

KW - Receptors, Calcitonin Gene-Related Peptide

KW - Vasodilator Agents

KW - Journal Article

KW - Randomized Controlled Trial

KW - Research Support, Non-U.S. Gov't

U2 - 10.1177/0333102410363491

DO - 10.1177/0333102410363491

M3 - Journal article

C2 - 20959429

VL - 30

SP - 1346

EP - 1353

JO - Cephalalgia

JF - Cephalalgia

SN - 0800-1952

IS - 11

ER -

ID: 168532410