Expression of Kv3.1b in the MNTB of normal hearing in congenitally deaf mice

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Expression of Kv3.1b in the MNTB of normal hearing in congenitally deaf mice

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dc.contributor Fyffe, Robert
dc.contributor.author Deardorff, Adam
dc.coverage.temporal 2010 en_US
dc.date.accessioned 2011-06-17T15:03:08Z
dc.date.available 2011-06-17T15:03:08Z
dc.date.created 2010-04
dc.date.issued 2010-04
dc.identifier.other celebration_abstract10_deardorff_a_2
dc.identifier.uri http://hdl.handle.net/2374.WSU/4761
dc.description.abstract

The medial nucleus of the trapezoid body (MNTB) is a key brainstem relay nucleus involved in sound localization. The primary excitatory input to MNTB principal cells is formed by specialized Calyx of Held synapses, arising from axons of globular bushy cells of the of the contralateral anteroventral cochlear nucleus (AVCN). Neurons in the MNTB are topographically organized according to a tonotopic map present throughout the auditory system. Cells responding best to high frequency stimulation are located medially within the nucleus, while cells responding best to low frequency stimulation are located laterally. A variety of mechanisms underlies MNTB synaptic response properties and discharge capabilities in accordance with the tonotopic map. One such mechanism is likely to be rapidly activating K+ currents.The functions of channels containing Kv3.1 subunits have been extensively characterized throughout the central nervous system. Within the MNTB, they contribute to a rapid high voltage activating K+ current that repolarizes action potentials (APs), facilitates high frequency firing, and aids in the faithful propagation of synaptic inputs. Further, tonotopically organized expression gradients of Kv3.1b have been demonstrated in several auditory brainstem nuclei including the rat MNTB, the avian nucleus mangocellularis, and mouse spiral ganglion. That these studies show stronger Kv3.1b expression in portions of the nucleus containing neurons with high characteristic frequency (CF), suggests such expression may correspond with other specializations in higher CF neurons allowing more rapid APs and higher transmission rates. The aim of this study is to determine 1) the distribution of Kv3.1b within the MNTB of normal hearing mice and 2) using a congenitally deaf (dn/dn) mouse model that lacks auditory nerve activity throughout development, if altered neural activity causes changes in the level and or pattern of Kv3.1b expression within the MNTB.

This presentation occurred at the Wright State University Campus-Wide Celebration of Research, Scholarship and Creative Activities on April 16, 2010

dc.language.iso en_US en_US
dc.publisher Wright State University en_US
dc.relation.ispartof Celebration of Research, Scholarship, and Creative Activities en_US
dc.rights.uri http://www.wright.edu/web/copyright.html
dc.subject Deardorff, Adam en_US
dc.subject Fyffe, Robert en_US
dc.subject Wright State University. Department of Neuroscience, Cell Biology and Physiology en_US
dc.title Expression of Kv3.1b in the MNTB of normal hearing in congenitally deaf mice en_US
dc.type Presentation en_US
dc.permissions World
dc.publisher.digital Digital Services Department, Wright State University Libraries en_US
dc.date.digitized 2010-04
dc.publisher.OLinstitution Wright State University

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