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[Abstract Title]. - Society for Neuroscience

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296. Learning and Memory: Physiology and Imaging III<br />

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

Program#/Poster#: 296.3/TT9<br />

Topic: F.02.i. Learning and memory: Physiology and imaging<br />

Support: NIH Grant MH58847<br />

NIH Grant MH071847<br />

<strong>Title</strong>: Modulation of correlated activity in primate entorhinal cortex cell pairs <strong>for</strong> well-learned<br />

associations compared to new associations<br />

Authors: *A. TAMBINI 1 , E. L. HARGREAVES 2 , W. A. SUZUKI 2 ;<br />

1 Ctr. <strong>for</strong> Neural Sci., 2 New York Univ., New York, NY<br />

<strong>Abstract</strong>: Several studies have shown that measures of correlated activity across cells can reflect<br />

complex cognitive operations, such as engaging working memory (Jones & Wilson, 2005) or<br />

goal selection and maintenance (Tsujimoto et al., 2008). Here we compared correlated activity in<br />

response to novel vs. very well-learned associations during the per<strong>for</strong>mance of a location-scene<br />

association task (Wirth et al., 2003). Animals initiated each trial by fixating on a central spot <strong>for</strong><br />

500 ms. Four identical targets superimposed on a complex visual scene were then presented <strong>for</strong><br />

500 ms followed by a 700 ms delay period, during which only the fixation spot and targets<br />

remained on the screen. The disappearance of the fixation spot cued the animal to make an eye<br />

movement to one of the four targets, of which only one was rewarded. Reward was followed by<br />

a 2000-3000 ms inter-trial interval period. Animals typically learned 2-4 new location-scene<br />

associations (new trials) together with 4 highly familiar “reference” associations (reference<br />

trials). We analyzed data from 210 entorhinal cortex cell pairs recorded from two monkeys. In<br />

order to determine the correlated activity across cell pairs, we computed the cross-correlation<br />

coefficient <strong>for</strong> different trial types and task periods <strong>for</strong> each pair. Since no a priori direction of<br />

spiking between cells was expected, we computed the bias corrected cross-correlation between<br />

cells with a window of ±25 ms. First, we asked if there were any differences in the overall<br />

correlations across the various trial periods <strong>for</strong> correctly executed new trials compared to<br />

correctly executed reference trials. We found significantly larger correlations in entorhinal cortex<br />

cell pairs in the scene, delay, and inter-trial interval periods of the task <strong>for</strong> reference trials<br />

compared to new trials (p

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