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dc.contributor.authorAmjad, Usamma
dc.contributor.authorChoi, Jiwon
dc.contributor.authorGibson, Daniel J
dc.contributor.authorMurray, Raymond
dc.contributor.authorGraybiel, Ann M
dc.contributor.authorSchwerdt, Helen N
dc.date.accessioned2026-04-08T15:43:31Z
dc.date.available2026-04-08T15:43:31Z
dc.date.issued2024-07
dc.identifier.urihttps://hdl.handle.net/1721.1/165364
dc.description.abstractMeasuring the dynamic relationship between neuromodulators, such as dopamine, and neuronal action potentials is imperative to understand how these fundamental modes of neural signaling interact to mediate behavior. We developed methods to measure concurrently dopamine and extracellular action potentials (i.e., spikes) in monkeys. Standard fast-scan cyclic voltammetric (FSCV) electrochemical (EChem) and electrophysiological (EPhys) recording systems are combined and used to collect spike and dopamine signals, respectively, from an array of carbon fiber (CF) sensors implanted in the monkey striatum. FSCV requires the application of small voltages at the implanted sensors to measure redox currents generated from target molecules, such as dopamine. These applied voltages create artifacts at neighboring EPhys measurement sensors which may lead to misclassification of these signals as physiological spikes. Therefore, simple automated temporal interpolation algorithms were designed to remove these artifacts and enable accurate spike extraction. We validated these methods using simulated artifacts and demonstrated an average spike recovery rate of 84.5%. We identified and discriminated cell type-specific units in the monkey striatum that were shown to correlate to specific behavioral task parameters related to reward size and eye movement direction. Synchronously recorded spike and dopamine signals displayed contrasting relations to the task variables, suggesting a complex relationship between these two modes of neural signaling. Future application of our methods will help advance our understanding of the interactions between neuromodulator signaling and neuronal activity, to elucidate more detailed mechanisms of neural circuitry and plasticity mediating behaviors in health and in disease.en_US
dc.language.isoen
dc.publisherSociety for Neuroscienceen_US
dc.relation.isversionofhttps://doi.org/10.1523/ENEURO.0001-24.2024en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceSociety for Neuroscienceen_US
dc.titleSynchronous Measurements of Extracellular Action Potentials and Neurochemical Activity with Carbon Fiber Electrodes in Nonhuman Primatesen_US
dc.typeArticleen_US
dc.identifier.citationUsamma Amjad, Jiwon Choi, Daniel J. Gibson, Raymond Murray, Ann M. Graybiel, Helen N. Schwerdt eNeuro 25 June 2024, 11 (7) ENEURO.0001-24.2024.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.relation.journaleNeuroen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2026-04-08T15:36:58Z
dspace.orderedauthorsAmjad, U; Choi, J; Gibson, DJ; Murray, R; Graybiel, AM; Schwerdt, HNen_US
dspace.date.submission2026-04-08T15:36:59Z
mit.journal.volume11en_US
mit.journal.issue7en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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