Migraine pain associated with middle cerebral artery dilatation: reversal by sumatriptan
- PMID: 1676084
- DOI: 10.1016/0140-6736(91)90005-a
Migraine pain associated with middle cerebral artery dilatation: reversal by sumatriptan
Abstract
The combination of measurements of regional cerebral blood flow (rCBF) and blood velocity in the middle cerebral arteries (MCA) by transcranial doppler sonography was used to investigate cerebrovascular involvement in migraine. Ten migraine patients with unilateral headache were studied during an attack and when they had been free of attacks for 5 days (non-attack). On both occasions they were given as intravenous infusion of sumatriptan (2 mg), a 5-HT1-like receptor agonist, which relieved the symptoms within 30 min without affecting rCBF. The MCA velocity was normal on both sides on the non-attack day and on the unaffected side during the attack. However, during the attack the MCA velocity on the headache side was significantly lower than that on the non-headache side (45 vs 61 cm/s:mean difference 16.3 [95% confidence interval 10.3-22.3]; p = 0.02). The MCA velocity on the headache side returned to normal after treatment with sumatriptan and recovery. Since rCBF in the MCA supply territory was unaffected, the lower velocity can be explained only by dilatation of the MCA. The mean MCA diameter increase was estimated to be 20%. Thus, headache was associated with intracranial large arterial dilatation on the headache side. Sumatriptan predominantly had effects on the distended artery, which suggests that the 5-HT receptor system has a role in the pathogenesis of migraine.
Comment in
-
Peripheral sympathetic activity during a migraine attack.Lancet. 1991 Oct 26;338(8774):1084-5. doi: 10.1016/0140-6736(91)91945-q. Lancet. 1991. PMID: 1681389 No abstract available.
Similar articles
-
Ergotamine, flunarizine and sumatriptan do not change cerebral blood flow velocity in normal subjects and migraneurs.J Neurol. 1991 Aug;238(5):245-50. doi: 10.1007/BF00319734. J Neurol. 1991. PMID: 1655985
-
Subcutaneous sumatriptan in the treatment of headache during withdrawal from drug-induced headache.Headache. 1991 Apr;31(4):205-9. doi: 10.1111/j.1526-4610.1991.hed3104205.x. Headache. 1991. PMID: 1646775 Clinical Trial.
-
Antimigraine drug sumatriptan increases blood flow velocity in large cerebral arteries during migraine attacks.Neurology. 1992 Aug;42(8):1522-6. doi: 10.1212/wnl.42.8.1522. Neurology. 1992. PMID: 1322512 Clinical Trial.
-
Rationale for the use of 5-HT1-like agonists in the treatment of migraine.J Neurol. 1991;238 Suppl 1:S57-61. doi: 10.1007/BF01642908. J Neurol. 1991. PMID: 1646289 Review.
-
Clinical effects and mechanism of action of sumatriptan in migraine.Clin Neurol Neurosurg. 1992;94 Suppl:S73-7. doi: 10.1016/0303-8467(92)90028-2. Clin Neurol Neurosurg. 1992. PMID: 1320526 Review.
Cited by
-
Calcitonin gene-related peptide (CGRP) modulates nociceptive trigeminovascular transmission in the cat.Br J Pharmacol. 2004 Aug;142(7):1171-81. doi: 10.1038/sj.bjp.0705807. Epub 2004 Jul 5. Br J Pharmacol. 2004. PMID: 15237097 Free PMC article.
-
Role of the 5-HT7 receptor in the central nervous system: from current status to future perspectives.Mol Neurobiol. 2011 Jun;43(3):228-53. doi: 10.1007/s12035-011-8175-3. Epub 2011 Mar 22. Mol Neurobiol. 2011. PMID: 21424680 Review.
-
Dural vasodilation causes a sensitization of rat caudal trigeminal neurones in vivo that is blocked by a 5-HT1B/1D agonist.Br J Pharmacol. 1999 Mar;126(6):1478-86. doi: 10.1038/sj.bjp.0702444. Br J Pharmacol. 1999. PMID: 10217543 Free PMC article.
-
Non-invasive methods for measuring vascular changes in neurovascular headaches.J Cereb Blood Flow Metab. 2019 Apr;39(4):633-649. doi: 10.1177/0271678X17724138. Epub 2017 Aug 7. J Cereb Blood Flow Metab. 2019. PMID: 28782410 Free PMC article. Review.
-
The effect of i.v. sumatriptan, a selective 5-HT1-receptor agonist on central haemodynamics and the coronary circulation.Br J Clin Pharmacol. 1992 Dec;34(6):541-6. Br J Clin Pharmacol. 1992. PMID: 1337261 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical