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Radkani, S.

Publications and source records attributed to Radkani, S..

2 recordsLinked to original sources

The predictive power of intrinsic timescale during the perceptual decision-making process across the mouse brain

Across the cortical hierarchy, single neurons are characterized by differences in the extent to which they can sustain their firing rate over time (i.e., their "intrinsic timescale"). Previous studies have demonstrated that neurons in a given brain region mostly exhibit either short or long intrinsic timescales. In this study, we sought to identify populations of neurons that accumulate information over different timescales in the mouse brain and to characterize their functions in the context of a visual discrimination task. Thus, we separately examined the neural population dynamics of neurons with long or short intrinsic timescales across different brain regions. More specifically, we looked at the decoding performance of these neural populations aligned to different task variables (stimulus onset, movement). Taken together, our population-level findings support the hypothesis that long intrinsic timescale neurons encode abstract variables related to decision formation. Furthermore, we investigated whether there was a relationship between how well a single neuron represents the animals choice or stimuli and their intrinsic timescale. We did not observe any significant relationship between the decoding of these task variables and a single neurons intrinsic timescale. In summary, our findings support the idea that the long intrinsic timescale population of neurons, which appear at different levels of the cortical hierarchy, are primarily more involved in representing the decision variable.

neuroscience↗

Distributed coding of evidence accumulation across the mouse brain using microcircuits with a diversity of timescales

The gradual accumulation of noisy evidence for or against options is the main step in the perceptual decision-making process. Using brain-wide electrophysiological recording in mice (Steinmetz et al., 2019), we examined neural correlates of evidence accumulation across brain areas. We demonstrated that the neurons with Drift-Diffusion-Model-like firing rate activity (i.e., evidence-sensitive ramping firing rate) were distributed across the brain. Exploring the underlying neural mechanism of evidence accumulation for the DDM-like neurons revealed different accumulation mechanisms (i.e. single and race) both within and across the brain areas. Our findings support the hypothesis that evidence accumulation is happening through multiple integration mechanisms in the brain. We further explored the timescale of the integration process in the single and race accumulator models. The results demonstrated that the accumulator microcircuits within each brain area had distinct properties in terms of their integration timescale, which were organized hierarchically across the brain. These findings support the existence of evidence accumulation over multiple timescales. Besides the variability of integration timescale across the brain, a heterogeneity of timescales was observed within each brain area as well. We demonstrated that this variability reflected the diversity of microcircuit parameters, such that accumulators with longer integration timescales had higher recurrent excitation strength.

neuroscience↗