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[Abstract Title]. - Society for Neuroscience

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Authors: N. ROTEM 1 , E. SESTIERI 3 , Y. YAROM 2 , *J. HOUNSGAARD 4 ;<br />

1 Dept. of Neurobiology/ The Otto Loewi Ctr., 2 Neurobio., Hebrew Univ., Jerusalem & Eilat,<br />

Israel; 3 Otto Loewi Minerva Ctr., Inter-University Inst., Eilat, Israel; 4 MFI, Panum Inst., 2200N<br />

Copenhagen, Denmark<br />

<strong>Abstract</strong>: Hair cell driven sensory systems track rapid changes in the environment. However,<br />

early processing of vestibular and auditory in<strong>for</strong>mation is complicated by a diversity of CNS<br />

projections with specialized primary afferent terminals and target neurons. In elasmobranches the<br />

near-body electric field is monitored by hair cells in Ampullae Lorenzini. This in<strong>for</strong>mation is<br />

transmitted exclusively to ascending efferent neurons (AENs) in the ipsilateral dorsal<br />

octavolateral brain stem nucleus. Thus, the precise goal-directed behaviors elicited by particular<br />

changes in the near-body electric field crucially depend on the fidelity of mapping primary<br />

afferent activity onto the AENs. Here we present the first study of transmission at this first<br />

synapse in early processing of electrosensory in<strong>for</strong>mation in the CNS.<br />

Intracellular recordings were obtained from AENs in the isolated brainstem from Iago omanensis<br />

sharks. Stimulating the anterior lateral line nerve selectively activated primary afferents (AFFs).<br />

Only monosynaptic excitatory responses were evoked by the stimulus. The range in stimulus<br />

intensity from just threshold to supramaximal intensity was narrow. In this range the synaptic<br />

response typically increased in amplitude from 0.5 to 4.5 mV. We noted that this increase was<br />

non-continuous. Indeed, amplitude histogram revealed clustering around 2-5 amplitude means.<br />

In most AENs the synaptic response evoked by an AFF stimulus readily elicited an action<br />

potential. Furthermore, the voltage threshold <strong>for</strong> action potentials was distinctly lower <strong>for</strong> AFF<br />

evoked response than <strong>for</strong> depolarization by intracellularly injected current and the synaptic<br />

response evoked by a parallel fiber stimulus. This suggests that each AEN is innervated by only<br />

few afferents that <strong>for</strong>m a highly efficient synaptic transmission.<br />

The response to AFF stimulation was depressed by paired stimulation. Paired-pulse depression<br />

reached a maximum with a delay of 30 ms and was observed at all stimulus intensities. The<br />

depression was not associated with a detectable postsynaptic conductance increase and inhibitory<br />

synaptic potential could not be discerned. Paired-pulse depression was blocked by bicculline and<br />

there<strong>for</strong>e most likely mediated by GABAA receptors. These observations suggest that pairedpulse<br />

depression is caused by presynaptic inhibition.<br />

In conclusion, electrosensory in<strong>for</strong>mation in the shark is mapped from primary afferents to AENs<br />

with minimal convergence. Each AEN is dominated by 2-5 afferents that <strong>for</strong>m robustly reliable<br />

excitatory synaptic connections. Temporal integration of electrosensory in<strong>for</strong>mation is regulated<br />

by feed-<strong>for</strong>ward presynaptic inhibition.<br />

Disclosures: N. Rotem, None; E. Sestieri, None; Y. yarom, None; J. Hounsgaard , None.<br />

Poster<br />

237. Synaptic Integration II<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm

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