13,786 research outputs found
Revealing ensemble state transition patterns in multi-electrode neuronal recordings using hidden Markov models
In order to harness the computational capacity of dissociated cultured neuronal networks, it is necessary to understand neuronal dynamics and connectivity on a mesoscopic scale. To this end, this paper uncovers dynamic spatiotemporal patterns emerging from electrically stimulated neuronal cultures using hidden Markov models (HMMs) to characterize multi-channel spike trains as a progression of patterns of underlying states of neuronal activity. However, experimentation aimed at optimal choice of parameters for such models is essential and results are reported in detail. Results derived from ensemble neuronal data revealed highly repeatable patterns of state transitions in the order of milliseconds in response to probing stimuli
Locally embedded presages of global network bursts
Spontaneous, synchronous bursting of neural population is a widely observed
phenomenon in nervous networks, which is considered important for functions and
dysfunctions of the brain. However, how the global synchrony across a large
number of neurons emerges from an initially non-bursting network state is not
fully understood. In this study, we develop a new state-space reconstruction
method combined with high-resolution recordings of cultured neurons. This
method extracts deterministic signatures of upcoming global bursts in "local"
dynamics of individual neurons during non-bursting periods. We find that local
information within a single-cell time series can compare with or even
outperform the global mean field activity for predicting future global bursts.
Moreover, the inter-cell variability in the burst predictability is found to
reflect the network structure realized in the non-bursting periods. These
findings demonstrate the deterministic mechanisms underlying the locally
concentrated early-warnings of the global state transition in self-organized
networks
Neural activity classification with machine learning models trained on interspike interval series data
The flow of information through the brain is reflected by the activity
patterns of neural cells. Indeed, these firing patterns are widely used as
input data to predictive models that relate stimuli and animal behavior to the
activity of a population of neurons. However, relatively little attention was
paid to single neuron spike trains as predictors of cell or network properties
in the brain. In this work, we introduce an approach to neuronal spike train
data mining which enables effective classification and clustering of neuron
types and network activity states based on single-cell spiking patterns. This
approach is centered around applying state-of-the-art time series
classification/clustering methods to sequences of interspike intervals recorded
from single neurons. We demonstrate good performance of these methods in tasks
involving classification of neuron type (e.g. excitatory vs. inhibitory cells)
and/or neural circuit activity state (e.g. awake vs. REM sleep vs. nonREM sleep
states) on an open-access cortical spiking activity dataset
Measuring spike train synchrony
Estimating the degree of synchrony or reliability between two or more spike
trains is a frequent task in both experimental and computational neuroscience.
In recent years, many different methods have been proposed that typically
compare the timing of spikes on a certain time scale to be fixed beforehand.
Here, we propose the ISI-distance, a simple complementary approach that
extracts information from the interspike intervals by evaluating the ratio of
the instantaneous frequencies. The method is parameter free, time scale
independent and easy to visualize as illustrated by an application to real
neuronal spike trains obtained in vitro from rat slices. In a comparison with
existing approaches on spike trains extracted from a simulated Hindemarsh-Rose
network, the ISI-distance performs as well as the best time-scale-optimized
measure based on spike timing.Comment: 11 pages, 13 figures; v2: minor modifications; v3: minor
modifications, added link to webpage that includes the Matlab Source Code for
the method (http://inls.ucsd.edu/~kreuz/Source-Code/Spike-Sync.html
Dopamine-modulated dynamic cell assemblies generated by the GABAergic striatal microcircuit
The striatum, the principal input structure of the basal ganglia, is crucial to both motor control and learning. It receives convergent input from all over the neocortex, hippocampal formation, amygdala and thalamus, and is the primary recipient of dopamine in the brain. Within the striatum is a GABAergic microcircuit that acts upon these inputs, formed by the dominant medium-spiny projection neurons (MSNs) and fast-spiking interneurons (FSIs). There has been little progress in understanding the computations it performs, hampered by the non-laminar structure that prevents identification of a repeating canonical microcircuit. We here begin the identification of potential dynamically-defined computational elements within the striatum. We construct a new three-dimensional model of the striatal microcircuit's connectivity, and instantiate this with our dopamine-modulated neuron models of the MSNs and FSIs. A new model of gap junctions between the FSIs is introduced and tuned to experimental data. We introduce a novel multiple spike-train analysis method, and apply this to the outputs of the model to find groups of synchronised neurons at multiple time-scales. We find that, with realistic in vivo background input, small assemblies of synchronised MSNs spontaneously appear, consistent with experimental observations, and that the number of assemblies and the time-scale of synchronisation is strongly dependent on the simulated concentration of dopamine. We also show that feed-forward inhibition from the FSIs counter-intuitively increases the firing rate of the MSNs. Such small cell assemblies forming spontaneously only in the absence of dopamine may contribute to motor control problems seen in humans and animals following a loss of dopamine cells. (C) 2009 Elsevier Ltd. All rights reserved
Connecting the Brain to Itself through an Emulation.
Pilot clinical trials of human patients implanted with devices that can chronically record and stimulate ensembles of hundreds to thousands of individual neurons offer the possibility of expanding the substrate of cognition. Parallel trains of firing rate activity can be delivered in real-time to an array of intermediate external modules that in turn can trigger parallel trains of stimulation back into the brain. These modules may be built in software, VLSI firmware, or biological tissue as in vitro culture preparations or in vivo ectopic construct organoids. Arrays of modules can be constructed as early stage whole brain emulators, following canonical intra- and inter-regional circuits. By using machine learning algorithms and classic tasks known to activate quasi-orthogonal functional connectivity patterns, bedside testing can rapidly identify ensemble tuning properties and in turn cycle through a sequence of external module architectures to explore which can causatively alter perception and behavior. Whole brain emulation both (1) serves to augment human neural function, compensating for disease and injury as an auxiliary parallel system, and (2) has its independent operation bootstrapped by a human-in-the-loop to identify optimal micro- and macro-architectures, update synaptic weights, and entrain behaviors. In this manner, closed-loop brain-computer interface pilot clinical trials can advance strong artificial intelligence development and forge new therapies to restore independence in children and adults with neurological conditions
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