5 research outputs found
Optimal stimulation protocol in a bistable synaptic consolidation model
Consolidation of synaptic changes in response to neural activity is thought
to be fundamental for memory maintenance over a timescale of hours. In
experiments, synaptic consolidation can be induced by repeatedly stimulating
presynaptic neurons. However, the effectiveness of such protocols depends
crucially on the repetition frequency of the stimulations and the mechanisms
that cause this complex dependence are unknown. Here we propose a simple
mathematical model that allows us to systematically study the interaction
between the stimulation protocol and synaptic consolidation. We show the
existence of optimal stimulation protocols for our model and, similarly to LTP
experiments, the repetition frequency of the stimulation plays a crucial role
in achieving consolidation. Our results show that the complex dependence of LTP
on the stimulation frequency emerges naturally from a model which satisfies
only minimal bistability requirements.Comment: 23 pages, 6 figure
How single neuron properties shape chaotic dynamics and signal transmission in random neural networks
While most models of randomly connected networks assume nodes with simple
dynamics, nodes in realistic highly connected networks, such as neurons in the
brain, exhibit intrinsic dynamics over multiple timescales. We analyze how the
dynamical properties of nodes (such as single neurons) and recurrent
connections interact to shape the effective dynamics in large randomly
connected networks. A novel dynamical mean-field theory for strongly connected
networks of multi-dimensional rate units shows that the power spectrum of the
network activity in the chaotic phase emerges from a nonlinear sharpening of
the frequency response function of single units. For the case of
two-dimensional rate units with strong adaptation, we find that the network
exhibits a state of "resonant chaos", characterized by robust, narrow-band
stochastic oscillations. The coherence of stochastic oscillations is maximal at
the onset of chaos and their correlation time scales with the adaptation
timescale of single units. Surprisingly, the resonance frequency can be
predicted from the properties of isolated units, even in the presence of
heterogeneity in the adaptation parameters. In the presence of these
internally-generated chaotic fluctuations, the transmission of weak,
low-frequency signals is strongly enhanced by adaptation, whereas signal
transmission is not influenced by adaptation in the non-chaotic regime. Our
theoretical framework can be applied to other mechanisms at the level of single
nodes, such as synaptic filtering, refractoriness or spike synchronization.
These results advance our understanding of the interaction between the dynamics
of single units and recurrent connectivity, which is a fundamental step toward
the description of biologically realistic network models in the brain, or, more
generally, networks of other physical or man-made complex dynamical units
Task-dependent optimal representations for cerebellar learning
The cerebellar granule cell layer has inspired numerous theoretical models of neural representations that support learned behaviors, beginning with the work of Marr and Albus. In these models, granule cells form a sparse, combinatorial encoding of diverse sensorimotor inputs. Such sparse representations are optimal for learning to discriminate random stimuli. However, recent observations of dense, low-dimensional activity across granule cells have called into question the role of sparse coding in these neurons. Here, we generalize theories of cerebellar learning to determine the optimal granule cell representation for tasks beyond random stimulus discrimination, including continuous input-output transformations as required for smooth motor control. We show that for such tasks, the optimal granule cell representation is substantially denser than predicted by classical theories. Our results provide a general theory of learning in cerebellum-like systems and suggest that optimal cerebellar representations are task-dependent