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dc.contributor.authorFriedman, Allyson K.
dc.contributor.authorJuarez, Barbara
dc.contributor.authorKu, Stacy M.
dc.contributor.authorZhang, Hongxing
dc.contributor.authorCalizo, Rhodora C.
dc.contributor.authorWalsh, Jessica J.
dc.contributor.authorChaudhury, Dipesh
dc.contributor.authorZhang, Song
dc.contributor.authorHawkins, Angel
dc.contributor.authorDietz, David M.
dc.contributor.authorMurrough, James W.
dc.contributor.authorRibadeneira, Maria
dc.contributor.authorWong, Erik H.
dc.contributor.authorNeve, Rachael L.
dc.contributor.authorHan, Ming-Hu
dc.date.accessioned2017-07-26T19:12:09Z
dc.date.available2017-07-26T19:12:09Z
dc.date.issued2016-05
dc.date.submitted2016-03
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1721.1/110861
dc.description.abstractLess than half of patients suffering from major depressive disorder, a leading cause of disability worldwide, achieve remission with current antidepressants, making it imperative to develop more effective treatment. A new therapeutic direction is emerging from the increased understanding of natural resilience as an active stress-coping process. It is known that potassium (K+) channels in the ventral tegmental area (VTA) are an active mediator of resilience. However, no druggable targets have been identified to potentiate active resilience mechanisms. In the chronic social defeat stress model of depression, we report that KCNQ-type K+ channel openers, including FDA-approved drug retigabine (ezogabine), show antidepressant efficacy. We demonstrate that overexpression of KCNQ channels in the VTA dopaminergic neurons and either local infusion or systemic administration of retigabine normalized neuronal hyperactivity and depressive behaviours. These findings identify KCNQ as a target for conceptually novel antidepressants that function through the potentiation of active resilience mechanisms.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). Ruth L. Kirschstein National Research Service Award (F31 MH095425)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). Ruth L. Kirschstein National Research Service Award (T32 MH 087004)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). Ruth L. Kirschstein National Research Service Award (F32 MH096464)en_US
dc.description.sponsorshipNational Institute of Mental Health (U.S.) (NIMH R01 MH092306)en_US
dc.language.isoen_US
dc.publisherSpringer Natureen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/ncomms11671en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleKCNQ channel openers reverse depressive symptoms via an active resilience mechanismen_US
dc.typeArticleen_US
dc.identifier.citationFriedman, Allyson K., Barbara Juarez, Stacy M. Ku, Hongxing Zhang, Rhodora C. Calizo, Jessica J. Walsh, Dipesh Chaudhury, et al. “KCNQ Channel Openers Reverse Depressive Symptoms via an Active Resilience Mechanism.” Nat Comms 7 (May 24, 2016): 11671.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.mitauthorNeve, Rachael L.
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsFriedman, Allyson K.; Juarez, Barbara; Ku, Stacy M.; Zhang, Hongxing; Calizo, Rhodora C.; Walsh, Jessica J.; Chaudhury, Dipesh; Zhang, Song; Hawkins, Angel; Dietz, David M.; Murrough, James W.; Ribadeneira, Maria; Wong, Erik H.; Neve, Rachael L.; Han, Ming-Huen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3854-5968
mit.licensePUBLISHER_CCen_US


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