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  4. The α6 subunit-containing GABA A receptor: A novel drug target for inhibition of trigeminal activation
 
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The α6 subunit-containing GABA A receptor: A novel drug target for inhibition of trigeminal activation

Journal
Neuropharmacology
Journal Volume
140
Pages
1-13
Date Issued
2018
Author(s)
PI-CHUAN FAN  
Lai T.-H.
Hor C.C.
Lee M.T.
Huang P.
Sieghart W.
Ernst M.
Knutson D.E.
Cook J.
LIH-CHU CHIOU  
DOI
10.1016/j.neuropharm.2018.07.017
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85053217858&doi=10.1016%2fj.neuropharm.2018.07.017&partnerID=40&md5=64325a31c7685e0c84c0bf46503d68f7
https://scholars.lib.ntu.edu.tw/handle/123456789/529202
Abstract
Novel treatments against migraine are an urgent medical requirement. The α6 subunit-containing GABA A receptors (α6GABA A Rs) are expressed in trigeminal ganglia (TG), the hub of the trigeminal vascular system (TGVS) that is involved in the pathogenesis of migraine. Here we reveal an unprecedented role of α6GABA A Rs in ameliorating TGVS activation using several pharmacological approaches in an animal model mimicking pathological changes in migraine. TGVS activation was induced by intra-cisternal (i.c.) instillation of capsaicin in Wistar rats. Centrally, i.c. capsaicin activated the trigeminal cervical complex (TCC) measured by the increased number of c-Fos-immunoreactive (c-Fos-ir) TCC neurons. Peripherally, it elevated calcitonin gene-related peptide immunoreactivity (CGRP-ir) in TG and depleted CGRP-ir in the dura mater. Pharmacological approaches included a recently identified α6GABA A R-selective positive allosteric modulator (PAM), the pyrazoloquinolinone Compound 6, two α6GABA A R-active PAMs (Ro15-4513 and loreclezole), an α6GABA A R-inactive benzodiazepine (diazepam), an α6GABA A R-selective antagonist (furosemide), and a clinically effective antimigraine agent (topiramate). We examined effects of these compounds on both central and peripheral TGVS responses induced by i.c. capsaicin. Compound 6 (3–10 mg/kg, i.p.) significantly attenuated the TCC neuronal activation and TG CGRP-ir elevation, and dural CGRP depletion induced by capsaicin. All these effects of Compound 6 were mimicked by topiramate, Ro15-4513 and loreclezole, but not by diazepam. The brain-impermeable furosemide antagonized the peripheral, but not central, effects of Compound 6. These results suggest that the α6GABA A R in TG is a novel drug target for TGVS activation and that α6GABA A R-selective PAMs have the potential to be developed as a novel pharmacotherapy for migraine.
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[SDGs]SDG3

Publisher
Elsevier Ltd
Type
journal article

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