Impact of Astroglial Connexins on Modafinil Pharmacological Properties

Modafinil is a non-amphetaminic wake-promoting compound used as therapy against sleepiness and narcolepsy. Its mode of action is complex, but modafinil has been recently proposed to act as a cellular-coupling enhancer in glial cells, through modulation of gap junctions constituted by connexins. The...

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Published inSleep (New York, N.Y.) Vol. 39; no. 6; pp. 1283 - 1292
Main Authors Duchêne, Adeline, Perier, Magali, Zhao, Yan, Liu, Xinhe, Thomasson, Julien, Chauveau, Frédéric, Piérard, Christophe, Lagarde, Didier, Picoli, Christèle, Jeanson, Tiffany, Mouthon, Franck, Dauvilliers, Yves, Giaume, Christian, Lin, Jian-Sheng, Charvériat, Mathieu
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 01.06.2016
Associated Professional Sleep Societies, LLC
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ISSN0161-8105
1550-9109
DOI10.5665/sleep.5854

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Summary:Modafinil is a non-amphetaminic wake-promoting compound used as therapy against sleepiness and narcolepsy. Its mode of action is complex, but modafinil has been recently proposed to act as a cellular-coupling enhancer in glial cells, through modulation of gap junctions constituted by connexins. The present study investigated in mice the impact of connexins on the effects of modafinil using connexin inhibitors. Modafinil was administered alone or combined with inhibitors of astrocyte connexin, meclofenamic acid, or flecainide, respectively, acting on Cx30 and Cx43. Sleep-wake states were monitored in wild-type and narcoleptic orexin knockout mice. A spontaneous alternation task was used to evaluate working memory in wild-type mice. The effects of the compounds on astroglial intercellular coupling were determined using dye transfer in acute cortical slices. Meclofenamic acid had little modulation on the effects of modafinil, but flecainide enhanced the wake-promoting and pro-cognitive effects of modafinil. Co-administration of modafinil/flecainide resulted in a marked decrease in the number and duration of direct transitions to rapid eye movement sleep, which are characteristic of narcoleptic episodes in orexin knockout mice. Furthermore, modafinil enhanced the connexin-mediated astroglial cell coupling, whereas flecainide reduced it. Finally, this modafinil-induced effect was reversed by co-administration with flecainide. Our study indicates that flecainide impacts the pharmacological effects of modafinil, likely through the normalization of Cx30-dependent gap junctional coupling in astroglial networks. The enhancement of the wake-promoting, behavioral, and cognitive outcomes of modafinil demonstrated here with flecainide would open new perspectives in the management of sleep disorders such as narcolepsy. A commentary on this article appears in this issue on page 1175.
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PMCID: PMC4863218
contributed equally to this paper
ISSN:0161-8105
1550-9109
DOI:10.5665/sleep.5854