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Modification of the visual response properties of cerebellar neurons by norepinephrine

dc.contributor.authorMoises, Hylan C.en_US
dc.contributor.authorBurne, Richard A.en_US
dc.contributor.authorWoodward, Donald J.en_US
dc.date.accessioned2006-04-10T13:45:40Z
dc.date.available2006-04-10T13:45:40Z
dc.date.issued1990-04-30en_US
dc.identifier.citationMoises, Hylan C., Burne, Richard A., Woodward, Donald J. (1990/04/30)."Modification of the visual response properties of cerebellar neurons by norepinephrine." Brain Research 514(2): 259-275. <http://hdl.handle.net/2027.42/28612>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6SYR-484778N-15D/2/aa0b0f28860b91f8b096a73c959bfee8en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28612
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2162710&dopt=citationen_US
dc.description.abstractExtracellular recordings were conducted in the paraflocculus of anesthetized Long-Evans pigmented rats to determine how iontophoresis of norepinephrine (NE) affects the responsiveness of individual Purkinje cells and interneurons to presentations of visual stimuli within their visual receptive fields. Presentations of moving or stationary visual stimuli during the control (pre-NE) period elicited simple spike excitations or inhibitory responses in slightly more than one-half (55%, n = 32) of the cells tested (20 of 38 Purkinje cells, 12 of 20 interneurons). The predominant effect of NE iontophoresis was to improve visually evoked responses in those neurons which showed modulations in their simple spike discharge to control presentations of visual stimuli. A clear enhancement of visual responses by NE (i.e., absolute increase over control) was observed in 18 of the units, and in 12 of the 14 remaining cells, reductions in stimulus-bound discharge during catecholamine iontophoresis were accompanied by much larger depressions in background activity, resulting in a net enhancement in the ratio of signal-to-noise. NE differentially affected responses to stimulus movement in the preferred and non-preferred direction in one-third of these neurons, such that directional selectivity was increased. However, the orientation bias of individual units was unchanged by NE. Iontophoretic application of the [beta]-adrenergic antagonist sotalol but not the [alpha]-adrenergic antagonist phentolamine blocked these facilitating noradrenergic effects. An additional feature of noradrenergic action was revealed in tests conducted in 26 cells which did not respond to control presentations of visual stimuli. Iontophoresis of NE resulted in the elicitation of visual responses in 11 of these units, suggesting the possibility that NE might act in some cases to gate the efficacy of subliminal synaptic input conveyed by classical afferent channels. It is proposed that an important aspect of noradrenergic action within local cerebellar circuits might be to refine the receptive field properties of individual neuronal elements and thereby improve information flow through the cerebellum.en_US
dc.format.extent1638818 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleModification of the visual response properties of cerebellar neurons by norepinephrineen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Physiology, The University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationotherAdvanced Technology Center, Allied-Bendix, Corp., Columbia, MD 21045, U.S.A.en_US
dc.contributor.affiliationotherDepartment of Cell Biology and Anatomy, The University of Texas Health Science Center at Dallas, Dallas, TX 75235, U.S.A.en_US
dc.identifier.pmid2162710en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28612/1/0000424.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-8993(90)91421-Cen_US
dc.identifier.sourceBrain Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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