Cortico-basal-ganglia-thalamic (CBGT) networks are critical for adaptive decision-making, yet how changes to circuit-level properties impact cognitive algorithms remains unclear. Here we explore how dopaminergic plasticity at corticostriatal synapses alters competition between striatal pathways, impacting the evidence accumulation process during decision-making. Spike-timing dependent plasticity simulations showed that dopaminergic feedback based on rewards modified the ratio of direct and indirect corticostriatal weights within opposing action channels. Using the learned weight ratios in a full spiking CBGT network model, we simulated neural dynamics and decision outcomes in a reward-driven decision task and fit them with a drift diffusion model. Fits revealed that the rate of evidence accumulation varied with inter-channel differences in direct pathway activity while boundary height varied with overall indirect pathway activity. This multi-level modeling approach demonstrates how complementary learning and decision computations can emerge from corticostriatal plasticity.
The question of how cortico-basal ganglia-thalamic (CBGT) pathways use dopaminergic feedback signals to modify future decisions has challenged computational neuroscientists for decades. Reviewing the literature on computational representations of dopaminergic corticostriatal plasticity, we show how the field is converging on a normative, synaptic-level learning algorithm that elegantly captures both neurophysiological properties of CBGT circuits and behavioral dynamics during reinforcement learning. Unfortunately, the computational studies that have led to this normative algorithmic model have all relied on simplified circuits that use abstracted actionselection rules. As a result, the application of this corticostriatal plasticity algorithm to a full model of the CBGT pathways immediately fails because the spatiotemporal distance between integration (corticostriatal circuits), action selection (thalamocortical loops) and learning (nigrostriatal circuits) means that the network does not know which synapses should be reinforced to favor previously rewarding actions. We show how observations from neurophysiology, in particular the sustained activation of selected action representations, can provide a simple means of resolving this credit assignment problem in models of CBGT learning. Using a biologically realistic spiking model of the full CBGT circuit, we demonstrate how this solution can allow a network to learn to select optimal targets and to relearn action-outcome contingencies when the environment changes. This simple illustration highlights how the normative framework for corticostriatal plasticity can be expanded to capture macroscopic network dynamics during learning and decision-making. | 2235RUBIN et al.
Cortico-basal-ganglia-thalamic (CBGT) networks are critical for adaptive decision-making, yet how changes to circuit-level properties impact cognitive algorithms remains unclear. Here we explore how dopaminergic plasticity at corticostriatal synapses alters competition between striatal pathways, impacting the evidence accumulation process during decision-making. Spike-timing dependent plasticity simulations showed that dopaminergic feedback based on rewards modified the ratio of direct and indirect corticostriatal weights within opposing action channels. Using the learned weight ratios in a full spiking CBGT network model, we simulated neural dynamics and decision outcomes in a reward-driven decision task and fit them with a drift diffusion model. Fits revealed that the rate of evidence accumulation varied with inter-channel differences in direct pathway activity while boundary height varied with overall indirect pathway activity. This multi-level modeling approach demonstrates how complementary learning and decision computations can emerge from corticostriatal plasticity. PLOS1/34 choice towards more rewarding actions. By mapping "up" the levels of analysis, this approach yields specific predictions about aspects of neuronal activity that map to the quantities appearing in the cognitive decision-making framework. 1 Introduction 1 The flexibility of mammalian behavior showcases the dynamic range over which 2 neural circuits can be modified by experience and the robustness of the emergent 3 cognitive algorithms that guide goal-directed actions. Decades of research in cognitive 4 science has independently detailed the algorithms of decision-making (e.g., 5 accumulation-to-bound models, [1]) and reinforcement learning (RL; [2, 3]), providing 6 foundational insights into the computational principles of adaptive decision-making. In 7 parallel, research in neuroscience has shown how the selection of actions, and the use of 8 feedback to modify selection processes, both rely on a common neural substrate: 9 cortico-basal ganglia-thalamic (CBGT) circuits [4-8]. 10 42 speed at which evidence accumulates in favor of one choice over another (see [20]). It 43 remains unclear how the dual-pathway organization of corticostriatal inputs contributes 44 to the representation and comparison of evidence for conflicting actions. Recent 45 theoretical models have proposed that decision evidence may be encoded as a dynamic 46 competition between the direct and indirect pathways within a single CBGT action 47 PLOS 2/34 57 behavior across neural and cognitive levels of analysis (Figure 1). Using a preliminary 58 spike-timing dependent plasticity (STDP; [24, 25]) simulation, we modeled how phasic 59 DA feedback signals [26] can modulate the relative balance of corticostriatal synapses, 60 thereby promoting or deterring action selection. The effects of learning on the synaptic 61 weights were incorporated into a spiking model of the full CBGT network meant to 62 capture the known physiological properties and connectivity patterns of the co...
We study the influence of subthreshold activity in the estimation of synaptic conductances when linear regression methods based on the current-voltage relationship are used. It is known that differences between actual conductances and the estimated ones using such methods can be huge in spiking regimes, so caution has been taken to remove spiking activity from many experimental data before proceeding to linear estimation. However, not much attention has been paid to the influence of ionic currents active in the non-spiking regime. We use a conductance-based model endowed both with an afterhyperpolarizing current and a low subthreshold current to show that the activity of these currents during subthreshold activity can lead to significant errors in synaptic conductance estimation (see Table 1 and Figure 1). More precisely, we found errors higher than 100% in the Figure 1 Representation of the relative errors in the I AHP and I LTS dominance phases. The pair of figures shows the relative error (dashed red), the estimated value (dotted black) and the actual value (solid black) of the synaptic, excitatory and inhibitory conductances, respectively, in the subthreshold regime. Vertical lines show the border between the I AHP -dominance (left) and I LTS -dominance (right) phases. The curves have been smoothed for a clearer plot. The actual values can be found in Table 1.Vich and Guillamon BMC Neuroscience 2014, 15(Suppl 1):P151
During action selection, mammals exhibit a high degree of flexibility in adapting their decisions in response to environmental changes. Although the cortico-basal ganglia-thalamic (CBGT) network is implicated in this adaptation, it features a synaptic architecture comprising multiple feed-forward, reciprocal, and feedback pathways, complicating efforts to elucidate the roles of specific CBGT populations in the process of evidence accumulation during decision-making. In this paper we apply a strategic sampling approach, based on Latin hypercube sampling, to explore how CBGT network properties, including subpopulation firing rates and synaptic weights, map to parameters of a normative drift diffusion model (DDM) representing algorithmic aspects of information accumulation during decision-making. Through the application of canonical correlation analysis, we find that this relationship can be characterized in terms of three low-dimensional control ensembles impacting specific qualities of the emergent decision policy: responsiveness (associated with overall activity in corticothalamic and direct pathways), pliancy (associated largely with overall activity in components of the indirect pathway of the basal ganglia), and choice (associated with differences in direct and indirect pathways across action channels). These analyses provide key mechanistic predictions about the roles of specific CBGT network elements in shifting different aspects of decision policies.
Subthreshold fluctuations in neuronal membrane potential traces contain nonlinear components, and employing nonlinear models might improve the statistical inference. We propose a new strategy to estimate synaptic conductances, which has been tested using in silico data and applied to in vivo recordings. The model is constructed to capture the nonlinearities caused by subthreshold activated currents, and the estimation procedure can discern between excitatory and inhibitory conductances using only one membrane potential trace. More precisely, we perform second order approximations of biophysical models to capture the subthreshold nonlinearities, resulting in quadratic integrate-and-fire models, and apply approximate maximum likelihood estimation where we only suppose that conductances are stationary in a 50–100 ms time window. The results show an improvement compared to existent procedures for the models tested here.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.