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dc.contributor.authorNieh, Horng-An Edward
dc.contributor.authorNamburi, Praneeth
dc.contributor.authorTye, Kay
dc.contributor.authorKim, Sung-Yon
dc.date.accessioned2015-01-15T18:00:28Z
dc.date.available2015-01-15T18:00:28Z
dc.date.issued2012-11
dc.date.submitted2012-11
dc.identifier.issn0006-8993
dc.identifier.urihttp://hdl.handle.net/1721.1/92890
dc.description.abstractThe neural circuits underlying emotional valence and motivated behaviors are several synapses away from both defined sensory inputs and quantifiable motor outputs. Electrophysiology has provided us with a suitable means for observing neural activity during behavior, but methods for controlling activity for the purpose of studying motivated behaviors have been inadequate: electrical stimulation lacks cellular specificity and pharmacological manipulation lacks temporal resolution. The recent emergence of optogenetic tools provides a new means for establishing causal relationships between neural activity and behavior. Optogenetics, the use of genetically-encodable light-activated proteins, permits the modulation of specific neural circuit elements with millisecond precision. The ability to control individual cell types, and even projections between distal regions, allows us to investigate functional connectivity in a causal manner. The greatest consequence of controlling neural activity with finer precision has been the characterization of individual neural circuits within anatomical brain regions as defined functional units. Within the mesolimbic dopamine system, optogenetics has helped separate subsets of dopamine neurons with distinct functions for reward, aversion and salience processing, elucidated GABA neuronal effects on behavior, and characterized connectivity with forebrain and cortical structures. Within the striatum, optogenetics has confirmed the opposing relationship between direct and indirect pathway medium spiny neurons (MSNs), in addition to characterizing the inhibition of MSNs by cholinergic interneurons. Within the hypothalamus, optogenetics has helped overcome the heterogeneity in neuronal cell-type and revealed distinct circuits mediating aggression and feeding. Within the amygdala, optogenetics has allowed the study of intra-amygdala microcircuitry as well as interconnections with distal regions involved in fear and anxiety. In this review, we will present the body of optogenetic studies that has significantly enhanced our understanding of emotional valence and motivated behaviors.en_US
dc.description.sponsorshipPicower Institute for Learning and Memory (Innovation Fund)en_US
dc.description.sponsorshipWhitehall Foundation (2012-08-45)en_US
dc.description.sponsorshipWade Awarden_US
dc.description.sponsorshipPicower Neurological Disorder Research Funden_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.description.sponsorshipIntegrative Neuronal Systems Center (Grant 6926328)en_US
dc.description.sponsorshipBrain and Cognitive Sciences Special Award (1497200)en_US
dc.description.sponsorshipMarcus Fellowship to Honor Norman B. Leventhal (3891441)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.brainres.2012.11.001en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleOptogenetic dissection of neural circuits underlying emotional valence and motivated behaviorsen_US
dc.typeArticleen_US
dc.identifier.citationNieh, Edward H., Sung-Yon Kim, Praneeth Namburi, and Kay M. Tye. “Optogenetic Dissection of Neural Circuits Underlying Emotional Valence and Motivated Behaviors.” Brain Research 1511 (May 2013): 73–92.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentPicower Institute for Learning and Memoryen_US
dc.contributor.mitauthorNieh, Horng-An Edwarden_US
dc.contributor.mitauthorNamburi, Praneethen_US
dc.contributor.mitauthorTye, Kayen_US
dc.relation.journalBrain Researchen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsNieh, Edward H.; Kim, Sung-Yon; Namburi, Praneeth; Tye, Kay M.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2154-6224
dc.identifier.orcidhttps://orcid.org/0000-0002-1410-8675
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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