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J Neurophysiol (April 17, 2003). doi:10.1152/jn.01169.2002
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Submitted on December 26, 2002
Accepted on February 10, 2003

Optical Detection of Developmental Origin of Synaptic Function in the Embryonic Chick Vestibulo-Cochlear Nuclei

Katsushige Sato1* and Yoko Momose-Sato1

1 Department of Physiology and Cell Biology, Tokyo Medical and Dental University, Graduate School and Faculty of Medicine, Tokyo, Japan

* To whom correspondence should be addressed. E-mail: katsushige.phy2{at}tmd.ac.jp.

Functional organization of the brainstem vestibulo-cochlear nuclei during embryogenesis was investigated using a multiple-site optical recording technique with a fast voltage-sensitive dye. Brainstem slices with the cochlear and/or vestibular nerves attached were dissected from 6- to 8-day old (E6 to E8) chick embryos. Electrical responses evoked by cochlear or vestibular nerve stimulation were optically recorded simultaneously from many loci of the preparations. In E7 and E8 preparations, we identified two components of the optical response with cochlear or vestibular nerve stimulation; one was a fast spike-like signal related to the action potential, and the other was a slow signal related to the glutamate-mediated excitatory postsynaptic potential. The location of the cochlear nerve response area was mainly located on the dorsolateral region, while that of the vestibular nerve was deviated ventro-medially. At E6, cochlear nerve stimulation evoked only the fast spike-like signals in normal Ringer's solution. However, when we removed Mg2+ from the extracellular solution, significant slow signals were elicited in the E6 preparation. The present results demonstrated that in the chick vestibulo-cochlear nuclei functional synapses are already generated by the E7 embryonic stage, and that postsynaptic activity related to NADA receptors emerges latently, at least in the cochlear nerve-related nucleus, at the E6 embryonic stage. This chronological sequence of the emergence of postsynaptic function is different from that reported previously (E10-E11), suggesting that the developmental origin of sensory information transfer in the auditory pathway is much earlier than has been anticipated.




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