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Graphic methods for the conventional rate-coding analysis and state-space analysis in the regression subspace. Conventional analysis (top and middle rows): in each single neuron, activity modulations by task variables are detected in the fixed time window (top row) using linear regression and ANOVA for continuous (left, Exp. 1) and categorical (right, Exp. 2) task parameters (Fig. 2, see for the task details), respectively. The same analyses were applied in a fine time resolution in Exp. 1 and Exp. 2 (middle row). The conventional analyses using a general linear model (linear regression and ANOVA) provide the extent of neural

Graphic methods for the conventional rate-coding analysis and state-space analysis in the regression subspace. Conventional analysis (top and middle rows): in each single neuron, activity modulations by task variables are detected in the fixed time window (top row) using linear regression and ANOVA for continuous (left, Exp. 1) and categorical (right, Exp. 2) task parameters (Fig. 2, see for the task details), respectively. The same analyses were applied in a fine time resolution in Exp. 1 and Exp. 2 (middle row). The conventional analyses using a general linear model (linear regression and ANOVA) provide the extent of neural

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Neural population dynamics provide a key computational framework for understanding information processing in the sensory, cognitive, and motor functions of the brain. They systematically depict complex neural population activity, dominated by strong temporal dynamics as trajectory geometry in a low-dimensional neural space. However, neural populati...

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... we showed that the general linear model usually used in the rate-coding model detects neural modulations using the same continuous and categorical parameters as a standard analysis procedure. This conventional approach can provide temporal changes in the selected metrics (e.g., proportion and extent of neural modulations; Fig. 4, top row), but they cannot provide trajectory geometry at the lower dimension. We note that detailed results from these conventional analyses have been previously reported (Chen and Naya, 2020, their Figs. 2, 5;Yamada et al., 2021, their Fig. ...
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... we used a general linear model to project a time series of each neural activity into a regression subspace composed of task parameters as continuous and categorical, as shown in the regression equations in Figure 4 (middle row, step 1; for details, see Materials and Methods). This step captures the across-trial variance caused by task-related parameters moment-by-moment at a population level, which demonstrates the extent of neural modulations by the task parameters across time. ...
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... at a population level, which demonstrates the extent of neural modulations by the task parameters across time. This corresponds to the estimation of the regression coefficients shown in Figure 3, E and J (for all time bins and conditions), which constructs the regression matrices detected in each neural population with a fine time resolution (Fig. 4, middle row, step 1, X). Second, we applied PCA one time to the time series of neural activity in the regression subspace in each neural population (Fig. 4, bottom row, step 2). This step determines the main features of the neural modulation signal across time in the predominant dimensions as trajectory geometry. These two steps identify how neural ...
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... regression coefficients shown in Figure 3, E and J (for all time bins and conditions), which constructs the regression matrices detected in each neural population with a fine time resolution (Fig. 4, middle row, step 1, X). Second, we applied PCA one time to the time series of neural activity in the regression subspace in each neural population (Fig. 4, bottom row, step 2). This step determines the main features of the neural modulation signal across time in the predominant dimensions as trajectory geometry. These two steps identify how neural modulations by task parameters change as a time series of eigenvectors in the regression ...
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... evaluated the properties of the extracted time series of the eigenvectors in the lower-dimensional space: the first three principal components (PC1 to PC3) in each neural population, in terms of vector angle, size, and deviance (Extended Data Fig. 4-1). The angles and sizes provide trajectory geometry that describes how neural modulation evolves after the visual presentation. ...
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... and for the six items and four locations; in total, 30 eigenvectors for each. Extended Data Figure 4-1 represents detail of the vector analyses. ...
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... at the population level by removing the average activity in each moment (Fig. 9, bottom row). Our methods are similar to the dPCA, but not the same. For example, we did not include the interaction component since the state-space analysis assumes a linear system. PCArs only focuses on neural dynamics in the subspace and requires only two steps (Fig. 4, middle, bottom rows) and minimal assumptions (orthogonality in the task design). Our PCArs is beneficial in terms of being simple and intuitive as it is an extension of the conventional rate-coding approach. Thus, our state-space analysis provides researchers with a significant advantage to find modulation dynamics in ...
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... this study, we evaluated neural modulation dynamics in terms of vector size, angle, and deviance in the regression subspace (Extended Data Fig. 4-1) that composes possible trajectory geometries. The combination of vector size and angle describes our straight geometry (i.e., constant angle), whereas deviance also reflects vector stability over time. ...

Citations

... Indeed, cortical inhibitory dysfunction results in various diseases including mental disorders (6,7). Since excitatory neurons constitute the majority of neurons at the core cortical center, the orbitofrontal cortex (OFC), they have been well examined in relation to economic behavior to obtain rewards (8)(9)(10)(11)(12)(13)(14). ...
... The identified FSNs accounted for approximately 12% (42/377; cOFC, n = 25; mOFC, n= 17) of the recorded OFC neurons. We previously reported the activity of RSNs (10, 12, 13) but not the activity of FSNs during the cued lottery task. We note that we did not record the OFC activity during choice task. ...
... We classified the FSNs as neurons in one cluster that exhibited narrow spike waveforms. In our previous reports (10,12,13,43), we reported the activity of RSNs but not of FSNs. The number of reported RSNs in this study differed from that in previous studies because we did not perform a quantitative classification of these neurons based on the waveform in those studies. ...
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Inhibitory interneurons are fundamental constituents of cortical circuits that process information to shape economic behaviors. However, the role of inhibitory interneurons in this process remains elusive at the core cortical reward-region, orbitofrontal cortex (OFC). Here, we show that presumed parvalbumin-containing GABAergic interneurons (fast-spiking neurons, FSNs) cooperate with presumed regular-spiking pyramidal neurons (RSNs) during economic-values computation. While monkeys perceived a visual lottery for probability and magnitude of rewards, identified FSNs occupied a small subset of OFC neurons (12%) with high-frequency firing-rates and wide dynamic-ranges, both are key intrinsic cellular characteristics to regulate cortical computation. We found that FSNs showed higher sensitivity to the probability and magnitude of rewards than RSNs. Unambiguously, both neural populations signaled expected values (i.e., probability times magnitude), but FSNs processed these reward's information strongly governed by the dynamic range. Thus, cooperative information processing between FSNs and RSNs provides a common cortical framework for computing economic values.
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Neural dynamics are thought to reflect computations that relay and transform information in the brain. Previous studies have identified the neural population dynamics in many individual brain regions as a trajectory geometry, preserving a common computational motif. However, whether these populations share particular geometric patterns across brain-wide neural populations remains unclear. Here, by mapping neural dynamics widely across temporal/frontal/limbic regions in the cortical and subcortical structures of monkeys, we show that 10 neural populations, including 2,500 neurons, propagate visual item information in a stochastic manner. We found that visual inputs predominantly evoked rotational dynamics in the higher-order visual area, TE, and its downstream striatum tail, while curvy/straight dynamics appeared frequently downstream in the orbitofrontal/hippocampal network. These geometric changes were not deterministic but rather stochastic according to their respective emergence rates. Our meta-analysis results indicate that visual information propagates as a heterogeneous mixture of stochastic neural population signals in the brain.