Abstract:The prefrontal cortex (PFC) is a key brain structure for decision making, behavioural flexibility and working memory. Neurons in PFC encode relevant stimuli through changes in their firing rate, although the metabolic cost of spiking activity puts strong constrains to neural codes based on firing rate modulation. Thus, how PFC neural populations code relevant information in an efficient way is not clearly understood. To address this issue we made single unit recordings in the PFC of rats performing a GO/NOGO d… Show more
“…In a recent study (Mininni et al . 20 ), we found that the coding capacity in PFC increases efficiently during stimuli presentation in a Go/NoGO discrimination task. Further theoretical considerations suggest that changes in PFC signal-to-noise correlation ratio induced by VTA dopamine neurons could explain our results.…”
Section: Introductionmentioning
confidence: 70%
“…Given that PFC neurons may code information by either increasing or decreasing their firing rate, we employed mutual information (MI) as a measure of information content in PFC to estimate the amount of information conveyed by neural activity regardless of the direction of firing rate changes. To this end, we first built a two-state neuron model that allowed a reliable estimation of MI 20 . In the model, we set the output of every neuron to ‘0’ or ‘1’ depending on whether the number of spikes within a given time window was lower/higher than the average computed in the same window across all correct GO and NoGO trials.…”
Section: Resultsmentioning
confidence: 99%
“…To study how much information is contained in the neuron population we built a binary neuron model that allows reliable estimation of pairwise Shannon entropy and mutual information 20 . The state of each neuron can be ‘1’ or ‘0’, depending on whether the number of spikes in a given time window was higher or lower than its average across all correct (GO and NoGO) trials.…”
It has been proposed that neuronal populations in the prefrontal cortex (PFC) robustly encode task-relevant information through an interplay with the ventral tegmental area (VTA). Yet, the precise computation underlying such functional interaction remains elusive. Here, we conducted simultaneous recordings of single-unit activity in PFC and VTA of rats performing a GO/NoGO task. We found that mutual information between stimuli and neural activity increases in the PFC as soon as stimuli are presented. Notably, it is the activity of putative dopamine neurons in the VTA that contributes critically to enhance information coding in the PFC. The higher the activity of these VTA neurons, the better the conditioned stimuli are encoded in the PFC.
“…In a recent study (Mininni et al . 20 ), we found that the coding capacity in PFC increases efficiently during stimuli presentation in a Go/NoGO discrimination task. Further theoretical considerations suggest that changes in PFC signal-to-noise correlation ratio induced by VTA dopamine neurons could explain our results.…”
Section: Introductionmentioning
confidence: 70%
“…Given that PFC neurons may code information by either increasing or decreasing their firing rate, we employed mutual information (MI) as a measure of information content in PFC to estimate the amount of information conveyed by neural activity regardless of the direction of firing rate changes. To this end, we first built a two-state neuron model that allowed a reliable estimation of MI 20 . In the model, we set the output of every neuron to ‘0’ or ‘1’ depending on whether the number of spikes within a given time window was lower/higher than the average computed in the same window across all correct GO and NoGO trials.…”
Section: Resultsmentioning
confidence: 99%
“…To study how much information is contained in the neuron population we built a binary neuron model that allows reliable estimation of pairwise Shannon entropy and mutual information 20 . The state of each neuron can be ‘1’ or ‘0’, depending on whether the number of spikes in a given time window was higher or lower than its average across all correct (GO and NoGO) trials.…”
It has been proposed that neuronal populations in the prefrontal cortex (PFC) robustly encode task-relevant information through an interplay with the ventral tegmental area (VTA). Yet, the precise computation underlying such functional interaction remains elusive. Here, we conducted simultaneous recordings of single-unit activity in PFC and VTA of rats performing a GO/NoGO task. We found that mutual information between stimuli and neural activity increases in the PFC as soon as stimuli are presented. Notably, it is the activity of putative dopamine neurons in the VTA that contributes critically to enhance information coding in the PFC. The higher the activity of these VTA neurons, the better the conditioned stimuli are encoded in the PFC.
Serotonin (5-HT) is a key neuromodulator of medial prefrontal cortex (mPFC) functions. Pharmacological manipulation of systemic 5-HT bioavailability alters the electrical activity of mPFC neurons. However, 5-HT modulation at the population level is not well characterized. In the present study, we made single neuron extracellular recordings in the mPFC of rats performing an operant conditioning task, and analyzed the effect of systemic administration of fluoxetine (a selective serotonin reuptake inhibitor) on the information encoded in the firing activity of the neural population. Chronic (longer than 15 days), but not acute (less than 15 days), fluoxetine administration reduced the firing rate of mPFC neurons. Moreover, fluoxetine treatment enhanced pairwise entropy but diminished noise correlation and redundancy in the information encoded, thus showing how mPFC differentially encodes information as a function of 5-HT bioavailability. Information about the occurrence of the reward-predictive stimulus was maximized during reward consumption, around 3 to 4 s after the presentation of the cue, and it was higher under chronic fluoxetine treatment. However, the encoded information was less robust to noise corruption when compared to control conditions.
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