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[Abstract Title]. - Society for Neuroscience

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<strong>Abstract</strong>: We determined the peak excitatory conductance necessary to reach threshold <strong>for</strong><br />

action potential (AP) generation in CA1 pyramidal cells (PCs) recorded in acute hippocampal<br />

slices obtained from 3-4 weeks old rats. PCs were initially recorded in the loose patch<br />

configuration and Schaffer collaterals stimulated at an intensity just sufficient to reach threshold<br />

<strong>for</strong> AP generation. We subsequently gained whole cell access to the neurons and determined the<br />

peak conductance of the underlying "threshold" excitatory postsynaptic current (EPSG) by<br />

holding the PC at the reversal potential <strong>for</strong> inhibition. We found that the threshold EPSG varied<br />

over a wide range, between 3 and 30 nS. The threshold EPSG correlated with the number of<br />

stimulated Schaffer collaterals. Both the variability in the threshold EPSG and the correlation<br />

with the number of activated Schaffer collaterals were abolished in the presence of the GABA A<br />

receptor antagonists gabazine. We determined the peak conductance of feed <strong>for</strong>ward inhibitory<br />

postsynaptic currents (IPSGs) elicited in response to stimulation of Schaffer collaterals at<br />

threshold <strong>for</strong> AP generation and found that it strongly correlated with the evoked threshold<br />

EPSG.<br />

These data suggest that the threshold excitation in PCs is not fixed but varies as a function of<br />

input strength. This variability depends on the presence of feed-<strong>for</strong>ward inhibition. By<br />

instantaneously adjusting pyramidal cell excitability to the strength of incoming activity, feed<strong>for</strong>ward<br />

inhibitory circuits allow the pyramidal cell population to be sensitive to weak stimuli yet<br />

not to saturate with stronger ones. This results in an expansion of the dynamic range of the CA1<br />

region to incoming activity.<br />

Disclosures: A. Marin-Burgin , None; F.R. Pouille, None; M. Scanziani, None.<br />

Poster<br />

237. Synaptic Integration II<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm<br />

Program#/Poster#: 237.5/D30<br />

Topic: B.07.c. Synaptic integration<br />

Support: Ribble Undergraduate Scholarship, University of Kentucky, Department of Biology<br />

<strong>Title</strong>: Comparison of the autonomic response of multiple sensory modalities in crayfish<br />

Authors: *M. M. ROBINSON, T. SPENCE, T. MCLAURINE, S. M. BIERBOWER, R. L.<br />

COOPER;<br />

Univ. Kentucky, Lexington, KY<br />

<strong>Abstract</strong>: Most organisms show diversity in the type and amount of peripheral sensors which<br />

allow <strong>for</strong> detection of different sensory stimuli within and across multiple sensory modalities.

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