Advances in understanding migraine pathophysiology: a bench to bedside review of research insights and therapeutics

被引:3
|
作者
Frimpong-Manson, Kofi [1 ]
Ortiz, Yuma T. [1 ]
McMahon, Lance R. [1 ]
Wilkerson, Jenny L. [1 ]
机构
[1] Texas Tech Univ, Dept Pharmaceut Sci, Hlth Sci Ctr, Amarillo, TX 79106 USA
来源
关键词
serotonin; calcitonin gene related peptide (CGRP); cannabinoid; rodent; cortical spreading depression; purinergic receptor; nitroglycerin; addiction; CORTICAL SPREADING DEPRESSION; GENE-RELATED PEPTIDE; CYCLASE-ACTIVATING POLYPEPTIDE; PATENT FORAMEN OVALE; VASOACTIVE-INTESTINAL-PEPTIDE; MAST-CELL DEGRANULATION; SPINAL; 5-HT7; RECEPTORS; BRAIN-STEM ACTIVATION; DOUBLE-BLIND; ADENYLATE-CYCLASE;
D O I
10.3389/fnmol.2024.1355281
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The individual and global burden of migraine is of such significance that there are accelerated efforts to develop new therapies. New migraine therapeutics are needed to address the current deficiencies that exist in the efficacy and adherence rate of approved anti-migraine medications. The recent discovery of the calcitonin gene related peptide as an add-on to the role of serotonin has markedly increased the range of new treatment options for acute and chronic migraine. Despite this, tackling the complexity of migraine disorders requires a complete understanding of its pathophysiology. Preclinical animal models can shed light on disease-related pathophysiology, including migraine. Indeed, the use of animal models has been instrumental in developing many therapeutics. However, an animal model is limited by the predictive and face validity of that model, and this extends to preclinical migraine models. In this review, a summary of the current understanding of the pathophysiology of migraine is given from both a preclinical and clinical perspective, and an emphasis is placed on the animal models of migraine. We will discuss the strengths and pitfalls of common preclinical migraine models as well as experimental research areas to explore further.
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页数:26
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