Search PubMed⌕ Search

Biomedical subjects

Jan Benda

Publications and source records attributed to Jan Benda.

5 recordsLinked to original sources

A synchronization-desynchronization code for natural communication signals.

Synchronous spiking of neural populations is hypothesized to play important computational roles in forming neural assemblies and solving the binding problem. Although the opposite phenomenon of desynchronization is well known from EEG studies, it is largely neglected on the neuronal level. We here provide an example of in vivo recordings from weakly electric fish demonstrating that, depending on the social context, different types of natural communication signals elicit transient desynchronization as well as synchronization of the electroreceptor population without changing the mean firing rate. We conclude that, in general, both positive and negative changes in the degree of synchrony can be the relevant signals for neural information processing.

Action Potentials↗

The cellular basis for parallel neural transmission of a high-frequency stimulus and its low-frequency envelope.

Sensory stimuli often have rich temporal and spatial structure. One class of stimuli that are common to visual and auditory systems and, as we show, the electrosensory system are signals that contain power in a narrow range of temporal (or spatial) frequencies. Characteristic of this class of signals is a slower variation in their amplitude, otherwise known as an envelope. There is evidence suggesting that, in the visual cortex, both narrowband stimuli and their envelopes are coded for in separate and parallel streams. The implementation of this parallel transmission is not well understood at the cellular level. We have identified the cellular basis for the parallel transmission of signal and envelope in the electrosensory system: a two-cell network consisting of an interneuron connected to a pyramidal cell by means of a slow synapse. This circuit could, in principle, be implemented in the auditory or visual cortex by the previously identified biophysics of cortical interneurons.

Animals↗

Spike-frequency adaptation separates transient communication signals from background oscillations.

Spike-frequency adaptation is a prominent feature of many neurons. However, little is known about its computational role in processing behaviorally relevant natural stimuli beyond filtering out slow changes in stimulus intensity. Here, we present a more complex example in which we demonstrate how spike-frequency adaptation plays a key role in separating transient signals from slower oscillatory signals. We recorded in vivo from very rapidly adapting electroreceptor afferents of the weakly electric fish Apteronotus leptorhynchus. The firing-frequency response of electroreceptors to fast communication stimuli ("small chirps") is strongly enhanced compared with the response to slower oscillations ("beats") arising from interactions of same-sex conspecifics. We are able to accurately predict the electroreceptor afferent response to chirps and beats, using a recently proposed general model for spike-frequency adaptation. The parameters of the model are determined for each neuron individually from the responses to step stimuli. We conclude that the dynamics of the rapid spike-frequency adaptation is sufficient to explain the data. Analysis of additional data from step responses demonstrates that spike-frequency adaptation acts subtractively rather than divisively as expected from depressing synapses. Therefore, the adaptation dynamics is linear and creates a high-pass filter with a cutoff frequency of 23 Hz that separates fast signals from slower changes in input. A similar critical frequency is seen in behavioral data on the probability of a fish emitting chirps as a function of beat frequency. These results demonstrate how spike-frequency adaptation in general can facilitate extraction of signals of different time scales, specifically high-frequency signals embedded in slower oscillations.

Action Potentials↗

A universal model for spike-frequency adaptation.

Spike-frequency adaptation is a prominent feature of neural dynamics. Among other mechanisms, various ionic currents modulating spike generation cause this type of neural adaptation. Prominent examples are voltage-gated potassium currents (M-type currents), the interplay of calcium currents and intracellular calcium dynamics with calcium-gated potassium channels (AHP-type currents), and the slow recovery from inactivation of the fast sodium current. While recent modeling studies have focused on the effects of specific adaptation currents, we derive a universal model for the firing-frequency dynamics of an adapting neuron that is independent of the specific adaptation process and spike generator. The model is completely defined by the neuron's onset f-I curve, the steady-state f-I curve, and the time constant of adaptation. For a specific neuron, these parameters can be easily determined from electrophysiological measurements without any pharmacological manipulations. At the same time, the simplicity of the model allows one to analyze mathematically how adaptation influences signal processing on the single-neuron level. In particular, we elucidate the specific nature of high-pass filter properties caused by spike-frequency adaptation. The model is limited to firing frequencies higher than the reciprocal adaptation time constant and to moderate fluctuations of the adaptation and the input current. As an extension of the model, we introduce a framework for combining an arbitrary spike generator with a generalized adaptation current.

Action Potentials↗

Energy integration describes sound-intensity coding in an insect auditory system.

We investigate the transduction of sound stimuli into neural responses and focus on locust auditory receptor cells. As in other mechanosensory model systems, these neurons integrate acoustic inputs over a fairly broad frequency range. To test three alternative hypotheses about the nature of this spectral integration (amplitude, energy, pressure), we perform intracellular recordings while stimulating with superpositions of pure tones. On the basis of online data analysis and automatic feedback to the stimulus generator, we systematically explore regions in stimulus space that lead to the same level of neural activity. Focusing on such iso-firing-rate regions allows for a rigorous quantitative comparison of the electrophysiological data with predictions from the three hypotheses that is independent of nonlinearities induced by the spike dynamics. We find that the dependence of the firing rates of the receptors on the composition of the frequency spectrum can be well described by an energy-integrator model. This result holds at stimulus onset as well as for the steady-state response, including the case in which adaptation effects depend on the stimulus spectrum. Predictions of the model for the responses to bandpass-filtered noise stimuli are verified accurately. Together, our data suggest that the sound-intensity coding of the receptors can be understood as a three-step process, composed of a linear filter, a summation of the energy contributions in the frequency domain, and a firing-rate encoding of the resulting effective sound intensity. These findings set quantitative constraints for future biophysical models.

Acoustic Stimulation↗