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dc.contributor.authorLu, Yi
dc.contributor.authorZhong, Cheng
dc.contributor.authorWang, Lulu
dc.contributor.authorWei, Pengfei
dc.contributor.authorHe, Wei
dc.contributor.authorHuang, Kang
dc.contributor.authorZhang, Yi
dc.contributor.authorZhan, Yang
dc.contributor.authorFeng, Guoping
dc.contributor.authorWang, Liping
dc.date.accessioned2017-05-12T22:42:46Z
dc.date.available2017-05-12T22:42:46Z
dc.date.issued2016-10
dc.date.submitted2015-12
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1721.1/109064
dc.description.abstractTemporal lobe epilepsy (TLE) is one of the most common drug-resistant forms of epilepsy in adults and usually originates in the hippocampal formations. However, both the network mechanisms that support the seizure spread and the exact directions of ictal propagation remain largely unknown. Here we report the dissection of ictal propagation in the hippocampal–entorhinal cortex (HP–EC) structures using optogenetic methods in multiple brain regions of a kainic acid-induced model of TLE in VGAT-ChR2 transgenic mice. We perform highly temporally precise cross-area analyses of epileptic neuronal networks and find a feed-forward propagation pathway of ictal discharges from the dentate gyrus/hilus (DGH) to the medial entorhinal cortex, instead of a re-entrant loop. We also demonstrate that activating DGH GABAergic interneurons can significantly inhibit the spread of ictal seizures and largely rescue behavioural deficits in kainate-exposed animals. These findings may shed light on future therapeutic treatments of TLE.en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/ncomms10962en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Publishing Groupen_US
dc.titleOptogenetic dissection of ictal propagation in the hippocampal–entorhinal cortex structuresen_US
dc.typeArticleen_US
dc.identifier.citationLu, Yi et al. “Optogenetic Dissection of Ictal Propagation in the Hippocampal–entorhinal Cortex Structures.” Nature Communications 7 (2016): 10962. © 2017 Macmillan Publishers Limiteden_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.mitauthorFeng, Guoping
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.orderedauthorsLu, Yi; Zhong, Cheng; Wang, Lulu; Wei, Pengfei; He, Wei; Huang, Kang; Zhang, Yi; Zhan, Yang; Feng, Guoping; Wang, Lipingen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8021-277X
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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