2,545 research outputs found
An axon initial segment is required for temporal precision in action potential encoding by neuronal populations
Central neurons initiate action potentials (APs) in the axon initial segment
(AIS), a compartment characterized by a high concentration of voltage-dependent
ion channels and specialized cytoskeletal anchoring proteins arranged in a
regular nanoscale pattern. Although the AIS was a key evolutionary innovation
in neurons, the functional benefits it confers are not clear. Using a mutation
of the AIS cytoskeletal protein \beta IV-spectrin, we here establish an in
vitro model of neurons with a perturbed AIS architecture that retains nanoscale
order but loses the ability to maintain a high NaV density. Combining
experiments and simulations we show that a high NaV density in the AIS is not
required for axonal AP initiation; it is however crucial for a high bandwidth
of information encoding and AP timing precision. Our results provide the first
experimental demonstration of axonal AP initiation without high axonal channel
density and suggest that increasing the bandwidth of the neuronal code and
hence the computational efficiency of network function was a major benefit of
the evolution of the AIS.Comment: Title adjusted, no other change
Gain control with A-type potassium current: IA as a switch between divisive and subtractive inhibition
Neurons process information by transforming barrages of synaptic inputs into
spiking activity. Synaptic inhibition suppresses the output firing activity of
a neuron, and is commonly classified as having a subtractive or divisive effect
on a neuron's output firing activity. Subtractive inhibition can narrow the
range of inputs that evoke spiking activity by eliminating responses to
non-preferred inputs. Divisive inhibition is a form of gain control: it
modifies firing rates while preserving the range of inputs that evoke firing
activity. Since these two "modes" of inhibition have distinct impacts on neural
coding, it is important to understand the biophysical mechanisms that
distinguish these response profiles.
We use simulations and mathematical analysis of a neuron model to find the
specific conditions for which inhibitory inputs have subtractive or divisive
effects. We identify a novel role for the A-type Potassium current (IA). In our
model, this fast-activating, slowly- inactivating outward current acts as a
switch between subtractive and divisive inhibition. If IA is strong (large
maximal conductance) and fast (activates on a time-scale similar to spike
initiation), then inhibition has a subtractive effect on neural firing. In
contrast, if IA is weak or insufficiently fast-activating, then inhibition has
a divisive effect on neural firing. We explain these findings using dynamical
systems methods to define how a spike threshold condition depends on synaptic
inputs and IA.
Our findings suggest that neurons can "self-regulate" the gain control
effects of inhibition via combinations of synaptic plasticity and/or modulation
of the conductance and kinetics of A-type Potassium channels. This novel role
for IA would add flexibility to neurons and networks, and may relate to recent
observations of divisive inhibitory effects on neurons in the nucleus of the
solitary tract.Comment: 20 pages, 11 figure
Gain Control With A-Type Potassium Current: IA As A Switch Between Divisive And Subtractive Inhibition
Neurons process and convey information by transforming barrages of synaptic inputs into spiking activity. Synaptic inhibition typically suppresses the output firing activity of a neuron, and is commonly classified as having a subtractive or divisive effect on a neuron’s output firing activity. Subtractive inhibition can narrow the range of inputs that evoke spiking activity by eliminating responses to non-preferred inputs. Divisive inhibition is a form of gain control: it modifies firing rates while preserving the range of inputs that evoke firing activity. Since these two “modes” of inhibition have distinct impacts on neural coding, it is important to understand the biophysical mechanisms that distinguish these response profiles. In this study, we use simulations and mathematical analysis of a neuron model to find the specific conditions (parameter sets) for which inhibitory inputs have subtractive or divisive effects. Significantly, we identify a novel role for the A-type Potassium current (IA). In our model, this fast-activating, slowly-inactivating outward current acts as a switch between subtractive and divisive inhibition. In particular, if IA is strong (large maximal conductance) and fast (activates on a time-scale similar to spike initiation), then inhibition has a subtractive effect on neural firing. In contrast, if IA is weak or insufficiently fast-activating, then inhibition has a divisive effect on neural firing. We explain these findings using dynamical systems methods (plane analysis and fast-slow dissection) to define how a spike threshold condition depends on synaptic inputs and IA. Our findings suggest that neurons can “self-regulate” the gain control effects of inhibition via combinations of synaptic plasticity and/or modulation of the conductance and kinetics of A-type Potassium channels. This novel role for IA would add flexibility to neurons and networks, and may relate to recent observations of divisive inhibitory effects on neurons in the nucleus of the solitary tract
Signal processing in local neuronal circuits based on activity-dependent noise and competition
We study the characteristics of weak signal detection by a recurrent neuronal
network with plastic synaptic coupling. It is shown that in the presence of an
asynchronous component in synaptic transmission, the network acquires
selectivity with respect to the frequency of weak periodic stimuli. For
non-periodic frequency-modulated stimuli, the response is quantified by the
mutual information between input (signal) and output (network's activity), and
is optimized by synaptic depression. Introducing correlations in signal
structure resulted in the decrease of input-output mutual information. Our
results suggest that in neural systems with plastic connectivity, information
is not merely carried passively by the signal; rather, the information content
of the signal itself might determine the mode of its processing by a local
neuronal circuit.Comment: 15 pages, 4 pages, in press for "Chaos
Synchronization of coupled stochastic limit cycle oscillators
For a class of coupled limit cycle oscillators, we give a condition on a
linear coupling operator that is necessary and sufficient for exponential
stability of the synchronous solution. We show that with certain modifications
our method of analysis applies to networks with partial, time-dependent, and
nonlinear coupling schemes, as well as to ensembles of local systems with
nonperiodic attractors. We also study robustness of synchrony to noise. To this
end, we analytically estimate the degree of coherence of the network
oscillations in the presence of noise. Our estimate of coherence highlights the
main ingredients of stochastic stability of the synchronous regime. In
particular, it quantifies the contribution of the network topology. The
estimate of coherence for the randomly perturbed network can be used as means
for analytic inference of degree of stability of the synchronous solution of
the unperturbed deterministic network. Furthermore, we show that in large
networks, the effects of noise on the dynamics of each oscillator can be
effectively controlled by varying the strength of coupling, which provides a
powerful mechanism of denoising. This suggests that the organization of
oscillators in a coupled network may play an important role in maintaining
robust oscillations in random environment. The analysis is complemented with
the results of numerical simulations of a neuronal network.
PACS: 05.45.Xt, 05.40.Ca
Keywords: synchronization, coupled oscillators, denoising, robustness to
noise, compartmental modelComment: major revisions; two new section
The impact of spike timing variability on the signal-encoding performance of neural spiking models
It remains unclear whether the variability of neuronal spike trains in vivo arises due to biological noise sources or represents highly precise encoding of temporally varying synaptic input signals. Determining the variability of spike timing can provide fundamental insights into the nature of strategies used in the brain to represent and transmit information in the form of discrete spike trains. In this study, we employ a signal estimation paradigm to determine how variability in spike timing affects encoding of random time-varying signals. We assess this for two types of spiking models: an integrate-and-fire model with random threshold and a more biophysically realistic stochastic ion channel model. Using the coding fraction and mutual information as information-theoretic measures, we quantify the efficacy of optimal linear decoding of random inputs from the model outputs and study the relationship between efficacy and variability in the output spike train. Our findings suggest that variability does not necessarily hinder signal decoding for the biophysically plausible encoders examined and that the functional role of spiking variability depends intimately on the nature of the encoder and the signal processing task; variability can either enhance or impede decoding performance
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