Strong inhibitory signaling underlies stable temporal dynamics and working memory in spiking neural networks

By analyzing computational models and neural data from the primate prefrontal cortex, the authors show that inhibitory-to-inhibitory signaling is critical for the stable temporal dynamics required for performing working memory tasks. Cortical neurons process information on multiple timescales, and areas important for working memory (WM) contain neurons capable of integrating information over a long timescale. However, the underlying mechanisms for the emergence of neuronal timescales stable enough to support WM are unclear. By analyzing a spiking recurrent neural network model trained on a WM task and activity of single neurons in the primate prefrontal cortex, we show that the temporal properties of our model and the neural data are remarkably similar. Dissecting our recurrent neural network model revealed strong inhibitory-to-inhibitory connections underlying a disinhibitory microcircuit as a critical component for long neuronal timescales and WM maintenance. We also found that enhancing inhibitory-to-inhibitory connections led to more stable temporal dynamics and improved task performance. Finally, we show that a network with such microcircuitry can perform other tasks without disrupting its pre-existing timescale architecture, suggesting that strong inhibitory signaling underlies a flexible WM network.

Automated summary

By analyzing computational models and neural data, the authors demonstrate that inhibitory-to-inhibitory signaling is crucial for maintaining stable temporal dynamics and working memory in the primate prefrontal cortex.