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Josef Ladenbauer

Publications and source records attributed to Josef Ladenbauer.

7 recordsLinked to original sources
arXiv2017

Low-dimensional spike rate models derived from networks of adaptive integrate-and-fire neurons: Comparison and implementation

The spiking activity of single neurons can be well described by a nonlinear integrate-and-fire model that includes somatic adaptation. When exposed to fluctuating inputs sparsely coupled populations of these model neurons exhibit stochastic collective dynamics that can be effectively characterized using the Fokker-Planck equation. [...] Here we derive from that description four simple models for the spike rate dynamics in terms of low-dimensional ordinary differential equations using two different reduction techniques: one uses the spectral decomposition of the Fokker-Planck operator, the other is based on a cascade of two linear filters and a nonlinearity, which are determined from the Fokker-Planck equation and semi-analytically approximated. We evaluate the reduced models for a wide range of biologically plausible input statistics and find that both approximation approaches lead to spike rate models that accurately reproduce the spiking behavior of the underlying adaptive integrate-and-fire population. [...] The low-dimensional models also well reproduce stable oscillatory spike rate dynamics that is generated by recurrent synaptic excitation and neuronal adaptation. [...] We have made available implementations that allow to numerically integrate the low-dimensional spike rate models as well as the Fokker-Planck partial differential equation in efficient ways for arbitrary model parametrizations as open source software. The derived spike rate descriptions retain a direct link to the properties of single neurons, allow for convenient mathematical analyses of network states, and are well suited for application in neural mass/mean-field based brain network models.

q-bio.NC↗
arXiv2016

Extending integrate-and-fire model neurons to account for the effects of weak electric fields and input filtering mediated by the dendrite

How extracellular electric fields, as generated endogenously or through transcranial brain stimulation, affect the dynamics of large neuronal populations is of great interest but not well understood. To study the collective dynamics of large populations single-compartment (point) model neurons have been proven very successful. These models, however, lack the dendritic morphology to biophysically account for the effects of electric fields, and for changes in synaptic integration due to morphology alone. Here we (i) characterize the response of a canonical spatial (ball-and-stick) model neuron to fluctuating synaptic input as well as an oscillatory, weak electric field, and (ii) analytically derive an extension for popular integrate-and-fire point neuron models to accurately reproduce these responses. We obtain distinct filters mediated by the dendrite for inputs at the soma (high-pass filter) or at the distal dendritic site (low-pass filter), and find that the electric field induces spike rate resonance in the beta and gamma frequency bands or even higher frequencies, depending on the location of synaptic background input. Due to their computational efficiency the extended point models are well suited for application in large populations of coupled neurons with different morphology, exposed to extracellular electric fields.

q-bio.NC↗
arXiv2016

Controlling Statistical Moments of Stochastic Dynamical Networks

We consider a general class of stochastic networks and ask which network nodes need to be controlled, and how, to stabilize and switch between desired metastable (target) states in terms of the first and second statistical moments of the system. We first show that it is sufficient to directly interfere with a subset of nodes which can be identified using information about the graph of the network only. Then, we develop a suitable method for feedback control which acts on that subset of nodes and preserves the covariance structure of the desired target state. Finally, we demonstrate our theoretical results using a stochastic Hopfield network and a global brain model. Our results are applicable to a variety of (model) networks, and further our understanding of the relationship between network structure and collective dynamics for the benefit of effective control.

nlin.AO↗
arXiv2013

How adaptation currents change threshold, gain and variability of neuronal spiking

Many types of neurons exhibit spike rate adaptation, mediated by intrinsic slow $\mathrm{K}^+$-currents, which effectively inhibit neuronal responses. How these adaptation currents change the relationship between in-vivo like fluctuating synaptic input, spike rate output and the spike train statistics, however, is not well understood. In this computational study we show that an adaptation current which primarily depends on the subthreshold membrane voltage changes the neuronal input-output relationship (I-O curve) subtractively, thereby increasing the response threshold. A spike-dependent adaptation current alters the I-O curve divisively, thus reducing the response gain. Both types of adaptation currents naturally increase the mean inter-spike interval (ISI), but they can affect ISI variability in opposite ways. A subthreshold current always causes an increase of variability while a spike-triggered current decreases high variability caused by fluctuation-dominated inputs and increases low variability when the average input is large. The effects on I-O curves match those caused by synaptic inhibition in networks with asynchronous irregular activity, for which we find subtractive and divisive changes caused by external and recurrent inhibition, respectively. Synaptic inhibition, however, always increases the ISI variability. We analytically derive expressions for the I-O curve and ISI variability, which demonstrate the robustness of our results. Furthermore, we show how the biophysical parameters of slow $\mathrm{K}^+$-conductances contribute to the two different types of adaptation currents and find that $\mathrm{Ca}^{2+}$-activated $\mathrm{K}^+$-currents are effectively captured by a simple spike-dependent description, while muscarine-sensitive or $\mathrm{Na}^+$-activated $\mathrm{K}^+$-currents show a dominant subthreshold component.

q-bio.NC↗
arXiv2013

Adaptation controls synchrony and cluster states of coupled threshold-model neurons

We analyze zero-lag and cluster synchrony of delay-coupled non-smooth dynamical systems by extending the master stability approach, and apply this to networks of adaptive threshold-model neurons. For a homogeneous population of excitatory and inhibitory neurons we find (i) that subthreshold adaptation stabilizes or destabilizes synchrony depending on whether the recurrent synaptic excitatory or inhibitory couplings dominate, and (ii) that synchrony is always unstable for networks with balanced recurrent synaptic inputs. If couplings are not too strong, synchronization properties are similar for very different coupling topologies, i.e., random connections or spatial networks with localized connectivity. We generalize our approach for two subpopulations of neurons with non-identical local dynamics, including bursting, for which activity-based adaptation controls the stability of cluster states, independent of a specific coupling topology.

nlin.AO↗
arXiv2013

Impact of adaptation currents on synchronization of coupled exponential integrate-and-fire neurons

Author summary: Synchronization of neuronal spiking in the brain is related to cognitive functions, such as perception, attention, and memory. It is therefore important to determine which properties of neurons influence their collective behavior in a network and to understand how. A prominent feature of many cortical neurons is spike frequency adaptation, which is caused by slow transmembrane currents. We investigated how these adaptation currents affect the synchronization tendency of coupled model neurons. Using the efficient adaptive exponential integrate-and-fire (aEIF) model and a biophysically detailed neuron model for validation, we found that increased adaptation currents promote synchronization of coupled excitatory neurons at lower spike frequencies, as long as the conduction delays between the neurons are negligible. Inhibitory neurons on the other hand synchronize in presence of conduction delays, with or without adaptation currents. Our results emphasize the utility of the aEIF model for computational studies of neuronal network dynamics. We conclude that adaptation currents provide a mechanism to generate low frequency oscillations in local populations of excitatory neurons, while faster rhythms seem to be caused by inhibition rather than excitation.

q-bio.NC↗