- Oral presentation
- Open Access
Inferred network from prefrontal cortex activity of rats unveils cell assemblies
© Tavoni et al; licensee BioMed Central Ltd. 2013
- Published: 8 July 2013
- External Input
- Sleep Phase
- Principal Eigenvector
- Large Entry
- Pearson Correlation Matrix
We analyzed recordings of prefrontal cortex activity of a rat in three different phases: while the animal faces a task in which a rule has to be learned and during the previous and subsequent sleep phases. We inferred an Ising model (characterized by binary variables and local fields and couplings as parameters) from the recorded spiking frequencies and pairwise correlations between neurons. We have shown how the inferred model can be used to deepen the analysis of the recordings, unveiling the presence of highly coordinated groups of neurons (cell assemblies), that is neurons that are activated together and synchronously inhibit the activity of other specific neurons.
We investigated the meaning of the external input parameter, discovering that it carries information on the time scale at which we observe correlations between neurons, namely the time bin width. In fact, the two curves of Figure 1A, which refer to the model inferred from the neuronal activity binned into two different time bins (10 ms and 30 ms), overlap by applying a translation of log(30 ms/10 ms) in the input strength. The fact that at Δt = 30 ms the first co-activated group appears for a small input strength H~1 means that the group is likely to be co-activated in a 30 ms time scale.
Neurons found in activated and inhibited groups extracted from our model correspond to large entries in the two principal eigenvectors of the Pearson correlation matrix obtained from the recorded activity. In particular the 1st component has large and positive entries on both activated groups, and the 2nd component shows negative entries on the 1st group, and positive ones on the 2nd group which entails that the groups can activate together or not. Moreover the activation of a group causes the inhibition of another group, which has also large entries on the 1st and 2nd components but with opposite signs. The sign of the components therefore refects in an intricate manner the activation-inhibition relationships between different groups.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.