05; MCC permutation test; Figure S5). To investigate whether D-AP5 affects local phase-synchronization of single units, we computed the spike-LFP pairwise phase consistency (PPC; Vinck et al., 2010, 2012). D-AP5 had a three-fold effect (Figures 5C and 5D; p < 0.05, MCC permutation test on T statistics). First, it strongly increased theta locking (∼10 Hz) by about 100%. Second, a beta (20–25 Hz) rhythm emerged, which was absent in the control condition. Third, it increased spike-LFP phase-locking in the supra-gamma range (110–160 Hz). Finally, we tested whether D-AP5 altered the relationship between neuronal

www.selleckchem.com/products/Dasatinib.html discrimination scores and spike-LFP phase-locking patterns. For the 0.5–1.0 s. period of odor sampling (during which ROC values peaked) we correlated the unit’s time-resolved Dcorrected ROC values with their spike-LFP PPC values, separately for D-AP5 and aCSF. Differences in Spearman-rank correlations between the drug and control condition were observed in the theta and supra-gamma range ( Figure 6A; p < 0.05; MCC permutation test). For the control condition, we found that spike-LFP theta PPC positively predicted Dcorrected, with significant correlations peaking ( Figure 6B; p < 0.05, MCC permutation test on difference in Spearman rhos) around the time when the Dcorrected values peaked (0.5–1 s after odor onset; Figure 3). However, in the same time window D-AP5 induced a

negative correlation between Talazoparib molecular weight Dcorrected and supra-gamma PPC values ( Figures 6A and 6C). In conditions where a unilateral NMDAR blockade in rat OFC did not affect task acquisition behavior and modestly increased task-related firing rates relative to baseline, we showed that this receptor plays a significant role in neural representations discriminating between stimulus-outcome conditions and plastic changes in firing patterns associated with learning these representations. Especially during odor processing and decision-making the capacity of OFC neurons to discriminate between cues predictive of different

Tryptophan synthase outcomes was impaired by NMDAR blockade. In addition, NMDAR blockade increased local rhythmic synchronization, as indexed by spike-LFP phase-locking, particularly in the theta (∼10 Hz), beta (20–30 Hz), and high-frequency range (110–150 Hz). Finally, we found a positive relationship between theta phase-locking and neuronal discrimination scores under control conditions, which was abolished by NMDAR blockade. One concern, when examining drug effects on neurophysiological correlates of cognitive processes, is that the drug may affect behavior, which could in turn affect firing patterns in OFC known to represent relevant behavioral task components (Pennartz et al., 2011a; Schoenbaum et al., 2009). Bilateral infusion of NMDAR antagonist in OFC has been shown to increase impulsive responding and impair reversal learning (Bohn et al., 2003b).