TY - JOUR
T1 - Opening of BKCa channels causes migraine attacks
T2 - a new downstream target for the treatment of migraine
AU - Al-Karagholi, Mohammad Al-Mahdi
AU - Ghanizada, Hashmat
AU - Waldorff Nielsen, Cherie Amalie
AU - Skandarioon, Camilla
AU - Snellman, Josefin
AU - Lopez-Lopez, Cristina
AU - Hansen, Jakob Møller
AU - Ashina, Messoud
N1 - Copyright © 2021 International Association for the Study of Pain.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Migraine is a common and frequently disabling neurological disorder, but the initiating migraine mechanisms are still poorly understood. Potassium channel opening may cause migraine, and we therefore examined the migraine-inducing effect of MaxiPost, a large (big)-conductance calcium-activated potassium (BKCa) channel opener, on migraine induction and cephalic vasodilation in individuals with migraine. Twenty-six patients with migraine without aura were randomly allocated to receive an infusion of MaxiPost or placebo on 2 study days separated by at least 1 week. The primary endpoint was the difference in incidence of migraine attacks after MaxiPost compared with placebo. The secondary endpoints were the difference in incidence of headaches and the difference in area under the curve for headache intensity scores (0-12 hours), for middle cerebral artery blood flow velocity (VMCA) (0-2 hours), and for superficial temporal artery and radial artery diameter. Twenty-two patients completed the study. Twenty-one of 22 (95%) developed migraine attacks after MaxiPost compared with none after placebo (P < 0.0001); the difference of incidence is 95% (95% confidence interval 86%-100%). The incidence of headache over the 12-hour observation period was higher after MaxiPost day (n = 22) than after placebo (n = 7) (P < 0.0001). We found a significant increase of VMCA and superficial temporal and radial arteries' diameter. Because BKCa channel opening initiates migraine attacks, we suggest that BKCa channel blockers could be potential candidates for novel antimigraine drugs.
AB - Migraine is a common and frequently disabling neurological disorder, but the initiating migraine mechanisms are still poorly understood. Potassium channel opening may cause migraine, and we therefore examined the migraine-inducing effect of MaxiPost, a large (big)-conductance calcium-activated potassium (BKCa) channel opener, on migraine induction and cephalic vasodilation in individuals with migraine. Twenty-six patients with migraine without aura were randomly allocated to receive an infusion of MaxiPost or placebo on 2 study days separated by at least 1 week. The primary endpoint was the difference in incidence of migraine attacks after MaxiPost compared with placebo. The secondary endpoints were the difference in incidence of headaches and the difference in area under the curve for headache intensity scores (0-12 hours), for middle cerebral artery blood flow velocity (VMCA) (0-2 hours), and for superficial temporal artery and radial artery diameter. Twenty-two patients completed the study. Twenty-one of 22 (95%) developed migraine attacks after MaxiPost compared with none after placebo (P < 0.0001); the difference of incidence is 95% (95% confidence interval 86%-100%). The incidence of headache over the 12-hour observation period was higher after MaxiPost day (n = 22) than after placebo (n = 7) (P < 0.0001). We found a significant increase of VMCA and superficial temporal and radial arteries' diameter. Because BKCa channel opening initiates migraine attacks, we suggest that BKCa channel blockers could be potential candidates for novel antimigraine drugs.
KW - Cross-Over Studies
KW - Double-Blind Method
KW - Headache
KW - Humans
KW - Middle Cerebral Artery
KW - Migraine Disorders/drug therapy
KW - BMS-204352
KW - Migraine
KW - Large (big)-conductance calcium-activated potassium channel
KW - Human models
KW - MaxiPost
UR - http://www.scopus.com/inward/record.url?scp=85106457630&partnerID=8YFLogxK
U2 - 10.1097/j.pain.0000000000002238
DO - 10.1097/j.pain.0000000000002238
M3 - Journal article
C2 - 34252916
VL - 162
SP - 2512
EP - 2520
JO - Pain
JF - Pain
SN - 0304-3959
IS - 10
ER -