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dc.contributor.authorRodrigues, Sen
dc.contributor.authorDesroches, Men
dc.contributor.authorKrupa, Men
dc.contributor.authorCortes, Jen
dc.contributor.authorAfia, Aen
dc.date.accessioned2018-08-13T10:44:23Z
dc.date.available2018-08-13T10:44:23Z
dc.date.issued2013-08-14en
dc.identifier.urihttp://hdl.handle.net/10026.1/12023
dc.description.abstract

Asynchronous and spontaneous neurotransmitter release remain elusive and constitute topics of considerable research both from the experimental and modeling perspective. This study proposes a parsimonious model that accounts for all modes of vesicle exocytosis and Short-Term Synaptic Plasticity (STSP). The modeling novelty is based on principles of slow-fast dynamical systems theory. The model's validity is shown by its good agreement with experimental data obtained from in vitro electrophysiological dual whole-cell recordings between local cholecystokinin (CKK)-positive, Schaffer collateral associated (SCA) interneurons in the CA1 region of rat hippocampus~\cite{AfiaAli2007,AfiaAli2010}. These unitary synapses display asynchronous release, governed by the retrograde release of endocannabinoid in response to post-synaptic membrane depolarisation. This work will advance our understanding of the physiology underlying differential exocytosis, and facilitate large-scale neuronal simulations.

en
dc.language.isoenen
dc.titleModel for (a)synchronous/spontaneous release, applied to CCK-positive Interneuron synapsesen
dc.typeReport
plymouth.confidentialfalseen
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering/School of Engineering, Computing and Mathematics
dc.rights.embargoperiodNot knownen
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.typeTechnical Reporten


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