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[Abstract Title]. - Society for Neuroscience

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indicative of reduced postsynaptic receptor sensitivity to glutamate transmission. ATPA, a<br />

kainate receptor agonist, mimics kainate action both pre- and post-synaptically. Domoic acid, a<br />

quisqualate receptor antagonist, blocks the postsynaptic receptors without depolarizing the<br />

muscle, which supports earlier findings of the muscle containing quisqualate subtype receptors.<br />

No effects are seen on the frequency of spontaneous events in low concentration of domoic acid<br />

which causes a 50% reduction in quantal amplitude. The results suggest a kainate pre-synaptic<br />

auto-inhibitory feedback on evoked release. The feedback could be partly responsible <strong>for</strong> the<br />

rapid depression with evoked high quantal release and facilitation with evoked low quantal<br />

release during repetitive stimulation. The mechanism of action within the presynaptic terminal<br />

remains to be elucidated. The mild direct postsynaptic action of kainate is likely due to partial<br />

antagonist action on the quisqualate receptors.<br />

Disclosures: J. Lee , None; D.M. Bhatt, None; D.M. Bhatt, None; W. Chung, None; N. Lee,<br />

None; R.L. Cooper, None.<br />

Poster<br />

237. Synaptic Integration II<br />

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

Program#/Poster#: 237.10/D35<br />

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

Support: 1R21 NS056124-01A1<br />

RO1 MH065924<br />

RO1 AA010983<br />

<strong>Title</strong>: Concentration-dependent dopamine modulation of recurrent synaptic activity and<br />

enhancement of signal-to-noise ratio in the prefrontal cortex<br />

Authors: *S. KROENER 1 , P. E. M. PHILLIPS 2 , L. J. CHANDLER 1 , J. K. SEAMANS 3 ;<br />

1 <strong>Neuroscience</strong>s, Med. Univ. South Carolina, Charleston, SC; 2 Dept. of Psychiatry & Behavioral<br />

Sci., Univ. of Washington, Seattle, WA; 3 Dept of Psychiatry and Brain Res. Ctr., Univ. of British<br />

Columbia, Vancouver, BC, Canada<br />

<strong>Abstract</strong>: The membrane potential of cortical neurons periodically shifts from a hyperpolarized<br />

down-state into a depolarized up-state which shapes synaptic integration and action potential<br />

generation. In the prefrontal cortex (PFC) the recurrent network activity that sustains the up-state<br />

may be modulated by dopamine (DA). Here we used organotypic co-cultures consisting of slices

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