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J Neurophysiol 96: 1215-1226, 2006. First published June 14, 2006; doi:10.1152/jn.00180.2006
0022-3077/06 $8.00
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Emergence of Action Potential Generation and Synaptic Transmission in Vestibular Nucleus Neurons

Mei Shao, June C. Hirsch and Kenna D. Peusner

Department of Anatomy and Cell Biology, George Washington University Medical Center, Washington, D.C.

Submitted 17 February 2006; accepted in final form 25 May 2006

Principal cells of the chick tangential nucleus are vestibular nucleus neurons in the hindbrain. Although detailed information is available on the morphogenesis of principal cells and synaptogenesis of primary vestibular fibers, this is the first study of their early functional development, when vestibular terminals emerge at embryonic days 10 and 13 (E10 and E13). At E10, 60% of principal cells generated spikes on depolarization, whereas 50% exhibited excitatory postsynaptic currents (EPSCs) on vestibular-nerve stimulation. The frequency was 0.2 Hz for glutamatergic spontaneous EPSCs (sEPSCs) at –60 mV, and 0.6 Hz for spontaneous inhibitory postsynaptic current (sIPSC) at +10 mV and completely GABAergic. All of these synaptic events were TTX-insensitive, miniature events. At E13, 50% of principal cells generated spikes on depolarization and 82% exhibited EPSCs on vestibular-nerve stimulation. The frequency was 0.7 Hz for sEPSCs at –60 mV, and 0.8 Hz for sIPSCs at +10 mV. Most principal cells had sIPSCs composed of both GABAergic (75%) and glycinergic (25%) events, but a few cells had only GABAergic sIPSCs. TTX decreased the frequency of EPSCs by 12%, and the IPSCs by 17%. In summary, at E10, some principal cells generated immature spikes on depolarization and EPSCs on vestibular-nerve stimulation. At E10, GABAergic events predominated, AMPA events had low frequencies, and glycinergic activity was absent. By E13, glycinergic events first appeared. This data were compared systematically to that obtained from the late-term embryo and hatchling to reveal the long-term sequence of changes in synaptic events and excitability and offer a broader understanding of how the vestibular system is assembled during development.


Address for reprint requests and other correspondence: K. D. Peusner, Dept. of Anatomy and Cell Biology, George Washington University Medical Center, 2300 I Street NW, Washington, DC 20037 (E-mail: anakdp{at}gwumc.edu)




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