Synaptic Zinc and Cortical Sensory Processing in the Laboratory Mouse

atmire.migration.oldid1915
dc.contributor.advisorDyck, Richard
dc.contributor.authorWu, Hsia-Pai Patrick
dc.date.accessioned2014-01-30T18:04:30Z
dc.date.available2014-03-15T07:00:21Z
dc.date.issued2014-01-30
dc.date.submitted2014en
dc.description.abstractA growing body of evidence indicates that synaptic zinc plays an important role in regulating neocortical neurotransmission. The goal of this thesis was to further examine the pattern of the distribution of synaptic zinc in the mammalian cortex and how synaptic zinc mediates synaptic transmission to affect cortical function and the generation of behaviour. The mouse visual cortex was used as a model system to observe the experience-dependent regulation of synaptic zinc levels. Histochemical analysis revealed that monocular deprivation dynamically altered the distribution of synaptic zinc in the deprived ocular domains of the visual cortex. Short (1 day) deprivation dramatically increased synaptic zinc density in layer IV of the deprived domains while long-term (3 months) deprivation elevated synaptic zinc levels in layers V and II/III. This result was similar to observations made in the visual cortex of cats and monkeys as well the barrel cortex of mice. The relationship between synaptic zinc in the barrel cortex and the processing of vibrissal sensory input was examined by assessing barrel cortex-dependent behaviour in a transgenic mouse that does not have synaptic zinc (ZnT3 KO mouse). A novel behavioural test that measured barrel cortex-dependent texture discrimination was devised and used to assay mystacial vibrissae function in ZnT3 KO mice. It was observed that ZnT3 KO mice retained the ability to use vibrissal tactile information to discriminate between textures but the acuity of the vibrissal sensory system was greatly reduced. In vivo voltage-sensitive dye imaging revealed that stimulation-evoked activity in the barrel cortex of ZnT3 KO mice is altered. Together, the results of this thesis suggest that synaptic zinc levels are dynamically modulated by sensory experience and that synaptic zinc contributes to the integration of sensory information within the primary sensory cortices.en_US
dc.identifier.citationWu, H. P. (2014). Synaptic Zinc and Cortical Sensory Processing in the Laboratory Mouse (Doctoral thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/27948en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/27948
dc.identifier.urihttp://hdl.handle.net/11023/1346
dc.language.isoeng
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectNeuroscience
dc.subject.classificationzincen_US
dc.subject.classificationsynaptic zincen_US
dc.subject.classificationvesicular zincen_US
dc.subject.classificationbarrel cortexen_US
dc.subject.classificationtexture discriminationen_US
dc.subject.classificationvisual cortex plasticityen_US
dc.subject.classificationcortical plasticityen_US
dc.subject.classificationsensory processingen_US
dc.titleSynaptic Zinc and Cortical Sensory Processing in the Laboratory Mouse
dc.typedoctoral thesis
thesis.degree.disciplinePsychology
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameDoctor of Philosophy (PhD)
ucalgary.item.requestcopytrue
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