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The execution of goal-oriented behaviours requires a spatially coherent alignment between sensory and motor maps. The current model for sensorimotor transformation in the superior colliculus relies on the topographic mapping of static spatial receptive fields onto movement endpoints1-6. Here, to experimentally assess the validity of this canonical static model of alignment, we dissected the visuo-motor network in the superior colliculus and performed in vivo intracellular and extracellular recordings across layers, in restrained and unrestrained conditions, to assess both the motor and the visual tuning of individual motor and premotor neurons. We found that collicular motor units have poorly defined visual static spatial receptive fields and respond instead to kinetic visual features, revealing the existence of a direct alignment in vectorial space between sensory and movement vectors, rather than between spatial receptive fields and movement endpoints as canonically hypothesized. We show that a neural network built according to these kinetic alignment principles is ideally placed to sustain ethological behaviours such as the rapid interception of moving and static targets. These findings reveal a novel dimension of the sensorimotor alignment process. By extending the alignment from the static to the kinetic domain this work provides a novel conceptual framework for understanding the nature of sensorimotor convergence and its relevance in guiding goal-directed behaviours.
Assuntos
Modelos Neurológicos , Movimento , Colículos Superiores , Percepção Visual , Animais , Feminino , Masculino , Objetivos , Cinética , Neurônios Motores/fisiologia , Movimento/fisiologia , Rede Nervosa/citologia , Rede Nervosa/fisiologia , Estimulação Luminosa , Desempenho Psicomotor/fisiologia , Reprodutibilidade dos Testes , Colículos Superiores/citologia , Colículos Superiores/fisiologia , Percepção Visual/fisiologiaRESUMO
Inhibitory neurons, although relatively few in number, exert powerful control over brain circuits. They stabilize network activity in the face of strong feedback excitation and actively engage in computations. Recent studies reveal the importance of a precise balance of excitation and inhibition in neural circuits, which often requires exquisite fine-tuning of inhibitory connections. We review inhibitory synaptic plasticity and its roles in shaping both feedforward and feedback control. We discuss the necessity of complex, codependent plasticity mechanisms to build nontrivial, functioning networks, and we end by summarizing experimental evidence of such interactions.
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Potenciais Pós-Sinápticos Inibidores/fisiologia , Rede Nervosa/fisiologia , Inibição Neural/fisiologia , Plasticidade Neuronal/fisiologia , Neurônios/fisiologia , Animais , Retroalimentação Fisiológica/fisiologia , Memória/fisiologia , Sinapses/fisiologiaRESUMO
Hebbian changes of excitatory synapses are driven by and further enhance correlations between pre- and postsynaptic activities. Hence, Hebbian plasticity forms a positive feedback loop that can lead to instability in simulated neural networks. To keep activity at healthy, low levels, plasticity must therefore incorporate homeostatic control mechanisms. We find in numerical simulations of recurrent networks with a realistic triplet-based spike-timing-dependent plasticity rule (triplet STDP) that homeostasis has to detect rate changes on a timescale of seconds to minutes to keep the activity stable. We confirm this result in a generic mean-field formulation of network activity and homeostatic plasticity. Our results strongly suggest the existence of a homeostatic regulatory mechanism that reacts to firing rate changes on the order of seconds to minutes.
Assuntos
Homeostase/fisiologia , Modelos Neurológicos , Plasticidade Neuronal/fisiologia , Neurônios/fisiologia , Sinapses/fisiologia , Potenciais de Ação , Biologia Computacional , Simulação por ComputadorRESUMO
When faced with a novel situation, people often spend substantial periods of time contemplating possible futures. For such planning to be rational, the benefits to behavior must compensate for the time spent thinking. Here, we capture these features of behavior by developing a neural network model where planning itself is controlled by the prefrontal cortex. This model consists of a meta-reinforcement learning agent augmented with the ability to plan by sampling imagined action sequences from its own policy, which we call 'rollouts'. In a spatial navigation task, the agent learns to plan when it is beneficial, which provides a normative explanation for empirical variability in human thinking times. Additionally, the patterns of policy rollouts used by the artificial agent closely resemble patterns of rodent hippocampal replays. Our work provides a theory of how the brain could implement planning through prefrontal-hippocampal interactions, where hippocampal replays are triggered by-and adaptively affect-prefrontal dynamics.
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Hipocampo , Redes Neurais de Computação , Córtex Pré-Frontal , Humanos , Hipocampo/fisiologia , Córtex Pré-Frontal/fisiologia , Modelos Neurológicos , Pensamento/fisiologia , Navegação Espacial/fisiologia , Reforço Psicológico , AnimaisRESUMO
Sequential activity reflecting previously experienced temporal sequences is considered a hallmark of learning across cortical areas. However, it is unknown how cortical circuits avoid the converse problem: producing spurious sequences that are not reflecting sequences in their inputs. We develop methods to quantify and study sequentiality in neural responses. We show that recurrent circuit responses generally include spurious sequences, which are specifically prevented in circuits that obey two widely known features of cortical microcircuit organization: Dale's law and Hebbian connectivity. In particular, spike-timing-dependent plasticity in excitation-inhibition networks leads to an adaptive erasure of spurious sequences. We tested our theory in multielectrode recordings from the visual cortex of awake ferrets. Although responses to natural stimuli were largely non-sequential, responses to artificial stimuli initially included spurious sequences, which diminished over extended exposure. These results reveal an unexpected role for Hebbian experience-dependent plasticity and Dale's law in sensory cortical circuits.
Assuntos
Modelos Neurológicos , Córtex Visual , Animais , Furões , Plasticidade Neuronal/fisiologia , Lobo Parietal , Córtex Visual/fisiologiaRESUMO
Across a range of motor and cognitive tasks, cortical activity can be accurately described by low-dimensional dynamics unfolding from specific initial conditions on every trial. These "preparatory states" largely determine the subsequent evolution of both neural activity and behavior, and their importance raises questions regarding how they are, or ought to be, set. Here, we formulate motor preparation as optimal anticipatory control of future movements and show that the solution requires a form of internal feedback control of cortical circuit dynamics. In contrast to a simple feedforward strategy, feedback control enables fast movement preparation by selectively controlling the cortical state in the small subspace that matters for the upcoming movement. Feedback but not feedforward control explains the orthogonality between preparatory and movement activity observed in reaching monkeys. We propose a circuit model in which optimal preparatory control is implemented as a thalamo-cortical loop gated by the basal ganglia.
Assuntos
Córtex Cerebral/fisiologia , Modelos Neurológicos , Vias Neurais/fisiologia , Desempenho Psicomotor/fisiologia , Tálamo/fisiologia , Animais , Antecipação Psicológica/fisiologia , Retroalimentação , HaplorrinosRESUMO
In both natural and engineered systems, communication often occurs dynamically over networks ranging from highly structured grids to largely disordered graphs. To use, or comprehend the use of, networks as efficient communication media requires understanding of how they propagate and transform information in the face of noise. Here, we develop a framework that enables us to examine how network structure, noise, and interference between consecutive packets jointly determine transmission performance in complex networks governed by linear dynamics. Mathematically, normal networks, which can be decomposed into separate low-dimensional information channels, suffer greatly from readout noise. Most details of their wiring have no impact on transmission quality. Non-normal networks, however, can largely cancel the effect of noise by transiently amplifying select input dimensions while ignoring others, resulting in higher net information throughput. Our theory could inform the design of new communication networks, as well as the optimal use of existing ones.
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Sensory cortices display a suite of ubiquitous dynamical features, such as ongoing noise variability, transient overshoots and oscillations, that have so far escaped a common, principled theoretical account. We developed a unifying model for these phenomena by training a recurrent excitatory-inhibitory neural circuit model of a visual cortical hypercolumn to perform sampling-based probabilistic inference. The optimized network displayed several key biological properties, including divisive normalization and stimulus-modulated noise variability, inhibition-dominated transients at stimulus onset and strong gamma oscillations. These dynamical features had distinct functional roles in speeding up inferences and made predictions that we confirmed in novel analyses of recordings from awake monkeys. Our results suggest that the basic motifs of cortical dynamics emerge as a consequence of the efficient implementation of the same computational function-fast sampling-based inference-and predict further properties of these motifs that can be tested in future experiments.
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Modelos Neurológicos , Redes Neurais de Computação , Córtex Visual/fisiologia , Vias Visuais/fisiologia , Animais , Haplorrinos , HumanosRESUMO
A major challenge in systems neuroscience is to understand how the dynamics of neural circuits give rise to behaviour. Analysis of complex dynamical systems is also at the heart of control engineering, where it is central to the design of robust control strategies. Although a rich engineering literature has grown over decades to facilitate the analysis of such systems, little of it has percolated into neuroscience so far. Here, we give a brief introduction to a number of core control-theoretic concepts that provide useful perspectives on neural circuit dynamics. We introduce important mathematical tools related to these concepts, and establish connections to neural circuit analysis, focusing on a number of themes that have arisen from the modern 'state-space' view on neural population dynamics.
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NeurociênciasRESUMO
Reliable information processing is a hallmark of many physical and biological networked systems. In this paper, we propose a novel framework for modelling information transmission within a linear dynamical network. Information propagation is modelled by means of a digital communication protocol that takes into account the realistic phenomenon of inter-symbol interference. Building on this framework, we adopt Shannon information rate to quantify the amount of information that can be reliably sent over the network within a fixed time window. We investigate how the latter information metric is affected by the connectivity structure of the network. Here, we focus in particular on networks characterized by a normal adjacency matrix. We show that for such networks the maximum achievable information rate depends only on the spectrum of the adjacency matrix. We then provide numerical results suggesting that non-normal network architectures could benefit information transmission in our framework.
RESUMO
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RESUMO
Classical work has viewed primary motor cortex (M1) as a controller of muscle and body dynamics. A recent brain-computer interface (BCI) experiment suggests a new, complementary perspective: M1 is itself a dynamical system under active control of other circuits.
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Interfaces Cérebro-Computador , Córtex Motor/fisiologia , Rede Nervosa/fisiologia , HumanosRESUMO
Correlated variability in cortical activity is ubiquitously quenched following stimulus onset, in a stimulus-dependent manner. These modulations have been attributed to circuit dynamics involving either multiple stable states ("attractors") or chaotic activity. Here we show that a qualitatively different dynamical regime, involving fluctuations about a single, stimulus-driven attractor in a loosely balanced excitatory-inhibitory network (the stochastic "stabilized supralinear network"), best explains these modulations. Given the supralinear input/output functions of cortical neurons, increased stimulus drive strengthens effective network connectivity. This shifts the balance from interactions that amplify variability to suppressive inhibitory feedback, quenching correlated variability around more strongly driven steady states. Comparing to previously published and original data analyses, we show that this mechanism, unlike previous proposals, uniquely accounts for the spatial patterns and fast temporal dynamics of variability suppression. Specifying the cortical operating regime is key to understanding the computations underlying perception.
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Neurônios/fisiologia , Córtex Visual/fisiologia , Animais , Macaca , Inibição Neural/fisiologia , Redes Neurais de Computação , Dinâmica não Linear , Lobo Occipital/citologia , Lobo Occipital/fisiologia , Córtex Visual/citologiaRESUMO
Motor cortex (M1) exhibits a rich repertoire of neuronal activities to support the generation of complex movements. Although recent neuronal-network models capture many qualitative aspects of M1 dynamics, they can generate only a few distinct movements. Additionally, it is unclear how M1 efficiently controls movements over a wide range of shapes and speeds. We demonstrate that modulation of neuronal input-output gains in recurrent neuronal-network models with a fixed architecture can dramatically reorganize neuronal activity and thus downstream muscle outputs. Consistent with the observation of diffuse neuromodulatory projections to M1, a relatively small number of modulatory control units provide sufficient flexibility to adjust high-dimensional network activity using a simple reward-based learning rule. Furthermore, it is possible to assemble novel movements from previously learned primitives, and one can separately change movement speed while preserving movement shape. Our results provide a new perspective on the role of modulatory systems in controlling recurrent cortical activity.
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Aprendizagem/fisiologia , Córtex Motor/fisiologia , Movimento/fisiologia , Rede Nervosa/fisiologia , Neurônios/fisiologia , Animais , Simulação por Computador , Modelos Neurológicos , Músculo Esquelético/fisiologiaRESUMO
Two theoretical studies reveal how networks of neurons may behave during reward-based learning.
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Modelos Neurológicos , Redes Neurais de Computação , Cognição , Simulação por Computador , AprendizagemRESUMO
Populations of neurons in motor cortex engage in complex transient dynamics of large amplitude during the execution of limb movements. Traditional network models with stochastically assigned synapses cannot reproduce this behavior. Here we introduce a class of cortical architectures with strong and random excitatory recurrence that is stabilized by intricate, fine-tuned inhibition, optimized from a control theory perspective. Such networks transiently amplify specific activity states and can be used to reliably execute multidimensional movement patterns. Similar to the experimental observations, these transients must be preceded by a steady-state initialization phase from which the network relaxes back into the background state by way of complex internal dynamics. In our networks, excitation and inhibition are as tightly balanced as recently reported in experiments across several brain areas, suggesting inhibitory control of complex excitatory recurrence as a generic organizational principle in cortex.
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Córtex Motor/fisiologia , Movimento/fisiologia , Rede Nervosa/fisiologia , Potenciais Sinápticos/fisiologia , Animais , Haplorrinos , Neurônios/fisiologia , Distribuição AleatóriaRESUMO
In dynamical models of cortical networks, the recurrent connectivity can amplify the input given to the network in two distinct ways. One is induced by the presence of near-critical eigenvalues in the connectivity matrix W, producing large but slow activity fluctuations along the corresponding eigenvectors (dynamical slowing). The other relies on W not being normal, which allows the network activity to make large but fast excursions along specific directions. Here we investigate the trade-off between non-normal amplification and dynamical slowing in the spontaneous activity of large random neuronal networks composed of excitatory and inhibitory neurons. We use a Schur decomposition of W to separate the two amplification mechanisms. Assuming linear stochastic dynamics, we derive an exact expression for the expected amount of purely non-normal amplification. We find that amplification is very limited if dynamical slowing must be kept weak. We conclude that, to achieve strong transient amplification with little slowing, the connectivity must be structured. We show that unidirectional connections between neurons of the same type together with reciprocal connections between neurons of different types, allow for amplification already in the fast dynamical regime. Finally, our results also shed light on the differences between balanced networks in which inhibition exactly cancels excitation and those where inhibition dominates.
Assuntos
Potenciais de Ação/fisiologia , Modelos Neurológicos , Modelos Estatísticos , Rede Nervosa/fisiologia , Inibição Neural/fisiologia , Plasticidade Neuronal/fisiologia , Animais , Simulação por Computador , HumanosRESUMO
Spike-frequency adaptation is known to enhance the transmission of information in sensory spiking neurons by rescaling the dynamic range for input processing, matching it to the temporal statistics of the sensory stimulus. Achieving maximal information transmission has also been recently postulated as a role for spike-timing-dependent plasticity (STDP). However, the link between optimal plasticity and STDP in cortex remains loose, as does the relationship between STDP and adaptation processes. We investigate how STDP, as described by recent minimal models derived from experimental data, influences the quality of information transmission in an adapting neuron. We show that a phenomenological model based on triplets of spikes yields almost the same information rate as an optimal model specially designed to this end. In contrast, the standard pair-based model of STDP does not improve information transmission as much. This result holds not only for additive STDP with hard weight bounds, known to produce bimodal distributions of synaptic weights, but also for weight-dependent STDP in the context of unimodal but skewed weight distributions. We analyze the similarities between the triplet model and the optimal learning rule, and find that the triplet effect is an important feature of the optimal model when the neuron is adaptive. If STDP is optimized for information transmission, it must take into account the dynamical properties of the postsynaptic cell, which might explain the target-cell specificity of STDP. In particular, it accounts for the differences found in vitro between STDP at excitatory synapses onto principal cells and those onto fast-spiking interneurons.