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dc.contributor.authorLi, Frederick Wai-Tsin
dc.date.accessioned2011-04-15T14:01:28Z
dc.date.available2011-04-15T14:01:28Z
dc.date.issued2011-04-15
dc.identifier.urihttp://hdl.handle.net/10222/13362
dc.description.abstractAlthough the perifornical lateral hypothalamic area (PeFLH), which contains orexin/hypocretin (OX) neurons, plays an important role in arousal-related behaviors, its neuromodulatory inputs are incompletely understood. The present study examined the role of glutamatergic inputs to the PeFLH in various arousal-related behaviors. Adult male rats received a microinjection of the ionotropic glutamate receptor agonists AMPA (1 and 2 mM) or NMDA (1 and 10 mM), or vehicle into the PeFLH, and were placed in an open field; 90 min later, rats were perfused for immunohistochemistry for OX and c-Fos as a marker of neuronal activation. AMPA injections dose-dependently increased locomotion, rearing, and drinking. NMDA injections (at 10 mM) increased locomotion and feeding. All these behaviors (except feeding) were positively correlated with the number of c-Fos/OX-immunoreactive neurons. These results support the role of ionotropic glutamate receptors on OX (and other) neurons in the PeFLH in the regulation of locomotor and ingestive behaviors.en_US
dc.language.isoen_USen_US
dc.subjectorexinen_US
dc.subjectlocomotor activityen_US
dc.subjectfeeding/drinkingen_US
dc.subjectc-Fosen_US
dc.titleANALYSIS OF BEHAVIORAL AND NEURONAL ACTIVATION FOLLOWING AMPA AND NMDA MICROINJECTIONS INTO THE PERIFORNICAL LATERAL HYPOTHALAMIC AREA IN RATSen_US
dc.date.defence2011-01-28
dc.contributor.departmentDepartment of Anatomy & Neurobiologyen_US
dc.contributor.degreeMaster of Scienceen_US
dc.contributor.external-examinerDr. Jennifer Stampen_US
dc.contributor.graduate-coordinatorDr. Kazue Sembaen_US
dc.contributor.thesis-readerDr. John Rutherforden_US
dc.contributor.thesis-readerDr. Douglas Rasmussonen_US
dc.contributor.thesis-supervisorDr. Kazue Sembaen_US
dc.contributor.ethics-approvalNot Applicableen_US
dc.contributor.manuscriptsNoen_US
dc.contributor.copyright-releaseNoen_US
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