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Clinical and animal pharmacology of migraine: new perspectives.

Abstract
Animal and clinical pharmacological studies show in certain vascular beds a biphasic action [potentiation and inhibition of serotonin (5-HT) responses] of some anti-migraine drugs, such as ergotamine, methysergide and more recently Org GC 94. Potentiation occurs at therapeutic drug concentrations. The present investigations seem to support the 5-HT theory of migraine and other essential headaches. In this theory, anti-migraine drugs, such as ergotamine, methysergide, pizotifen, and Org GC 94 could reduce the occurrence of pain in migraine and other esscutial headaches by acting as partial agonists tending to correct a deficiency of central 5-HT concentrations or turnover.
AuthorsB Anselmi, P L Del Bianco, C J de Vos, P Galli, J C Lamar, E Schönbaum, F Sicuteri, F van der Veen
JournalMonographs in neural sciences (Monogr Neural Sci) Vol. 3 Pg. 45-59 ( 1976) ISSN: 0300-5186 [Print] Switzerland
PMID979997 (Publication Type: Journal Article)
Chemical References
  • Bronchodilator Agents
  • Dibenzoxazepines
  • Serotonin Antagonists
  • Vasoconstrictor Agents
Topics
  • Animals
  • Bronchodilator Agents
  • Dibenzoxazepines (metabolism, pharmacology)
  • Dogs
  • Female
  • Guinea Pigs
  • In Vitro Techniques
  • Male
  • Migraine Disorders (physiopathology)
  • Muscle Contraction (drug effects)
  • Nose (blood supply)
  • Rats
  • Regional Blood Flow (drug effects)
  • Serotonin Antagonists
  • Stomach (drug effects)
  • Time Factors
  • Uterus (drug effects)
  • Vasoconstrictor Agents

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