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dc.contributor.authorLi, Wenchang
dc.contributor.authorMerrison-Hort, Robert
dc.contributor.authorZhang, Hong Yan
dc.contributor.authorBorisyuk, Roman
dc.date.accessioned2014-05-15T15:31:11Z
dc.date.available2014-05-15T15:31:11Z
dc.date.issued2014-04-23
dc.identifier.citationLi , W , Merrison-Hort , R , Zhang , H Y & Borisyuk , R 2014 , ' The generation of antiphase oscillations and synchrony by a rebound-based vertebrate central pattern generator ' , The Journal of Neuroscience , vol. 34 , no. 17 , pp. 6065-77 . https://doi.org/10.1523/JNEUROSCI.4198-13.2014en
dc.identifier.issn0270-6474
dc.identifier.otherPURE: 117052413
dc.identifier.otherPURE UUID: 36bde9f0-8ef1-462b-b18d-6139ed2ff6a6
dc.identifier.otherScopus: 84899482774
dc.identifier.otherWOS: 000334929100034
dc.identifier.otherORCID: /0000-0002-1179-6636/work/64361121
dc.identifier.urihttps://hdl.handle.net/10023/4804
dc.description.abstractMany neural circuits are capable of generating multiple stereotyped outputs after different sensory inputs or neuromodulation.We have previously identified the central pattern generator (CPG) forXenopustadpole swimming that involves antiphase oscillations of activitybetween the left and right sides. Here we analyze the cellular basis for spontaneous left–right motor synchrony characterized by simul-taneous bursting on both sides at twice the swimming frequency. Spontaneous synchrony bouts are rare in most tadpoles, and theyinstantly emerge from and switch back to swimming, most frequently within the first second after skin stimulation. Analyses show thatonly neurons that are active during swimming fire action potentials in synchrony, suggesting both output patterns derive from the sameneural circuit. The firing of excitatory descending interneurons (dINs) leads that of other types of neurons in synchrony as it does inswimming. During synchrony, the time window between phasic excitation and inhibition is 7.91 ms, shorter than that in swimming (412.3 ms). The occasional, extra midcycle firing of dINs during swimming may initiate synchrony, and mismatches of timing in theleft and right activity can switch synchrony back to swimming. Computer modeling supports these findings by showing that the sameneural network, in which reciprocal inhibition mediates rebound firing, can generate both swimming and synchrony without circuitreconfiguration. Modeling also shows that lengthening the time window between phasic excitation and inhibition by increasing dINsynaptic/conduction delay can improve the stability of synchrony.
dc.format.extent13
dc.language.isoeng
dc.relation.ispartofThe Journal of Neuroscienceen
dc.rights© 2014 Li et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.en
dc.subjectCentral patten generatoren
dc.subjectLocomotionen
dc.subjectOscillationsen
dc.subjectSpinal corden
dc.subjectSwimmingen
dc.subjectSynchronyen
dc.subjectQH301 Biologyen
dc.subject.lccQH301en
dc.titleThe generation of antiphase oscillations and synchrony by a rebound-based vertebrate central pattern generatoren
dc.typeJournal articleen
dc.contributor.sponsorThe Wellcome Trusten
dc.contributor.sponsorThe Royal Societyen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Psychology and Neuroscienceen
dc.contributor.institutionUniversity of St Andrews. Institute of Behavioural and Neural Sciencesen
dc.identifier.doihttps://doi.org/10.1523/JNEUROSCI.4198-13.2014
dc.description.statusPeer revieweden
dc.identifier.grantnumber089319/Z/09/Zen
dc.identifier.grantnumber516002.K5880/ROGen


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