TY - JOUR
T1 - Could Experimental Inflammation Provide Better Understanding of Migraines?
AU - Reducha, Philip Victor
AU - Edvinsson, Lars
AU - Haanes, Kristian Agmund
PY - 2022
Y1 - 2022
N2 - Migraines constitute a common neurological and headache disorder affecting around 15% of the world's population. In addition to other mechanisms, neurogenic neuroinflammation has been proposed to play a part in migraine chronification, which includes peripheral and central sensitization. There is therefore considerable evidence suggesting that inflammation in the intracranial meninges could be a key element in addition to calcitonin gene-related peptide (CGRP), leading to sensitization of trigeminal meningeal nociceptors in migraines. There are several studies that have utilized this approach, with a strong focus on using inflammatory animal models. Data from these studies show that the inflammatory process involves sensitization of trigeminovascular afferent nerve terminals. Further, by applying a wide range of different pharmacological interventions, insight has been gained on the pathways involved. Importantly, we discuss how animal models should be used with care and that it is important to evaluate outcomes in the light of migraine pathology.
AB - Migraines constitute a common neurological and headache disorder affecting around 15% of the world's population. In addition to other mechanisms, neurogenic neuroinflammation has been proposed to play a part in migraine chronification, which includes peripheral and central sensitization. There is therefore considerable evidence suggesting that inflammation in the intracranial meninges could be a key element in addition to calcitonin gene-related peptide (CGRP), leading to sensitization of trigeminal meningeal nociceptors in migraines. There are several studies that have utilized this approach, with a strong focus on using inflammatory animal models. Data from these studies show that the inflammatory process involves sensitization of trigeminovascular afferent nerve terminals. Further, by applying a wide range of different pharmacological interventions, insight has been gained on the pathways involved. Importantly, we discuss how animal models should be used with care and that it is important to evaluate outcomes in the light of migraine pathology.
KW - inflammation
KW - migraine
KW - CGRP
KW - CFA
KW - inflammatory soup
KW - TRIGEMINAL GANGLION NEURONS
KW - GENE-RELATED PEPTIDE
KW - MAGNETIC-RESONANCE-SPECTROSCOPY
KW - CGRP RECEPTOR ANTAGONIST
KW - RAT MODEL
KW - CENTRAL SENSITIZATION
KW - PLASMA EXTRAVASATION
KW - ANIMAL-MODEL
KW - MITOCHONDRIAL DYSFUNCTION
KW - MENINGEAL NOCICEPTORS
U2 - 10.3390/cells11152444
DO - 10.3390/cells11152444
M3 - Review
C2 - 35954288
SN - 2073-4409
VL - 11
JO - Cells
JF - Cells
IS - 15
M1 - 2444
ER -