49,842 research outputs found
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
Inhibitory synchrony as a mechanism for attentional gain modulation
Recordings from area V4 of monkeys have revealed that when the focus of
attention is on a visual stimulus within the receptive field of a cortical
neuron, two distinct changes can occur: The firing rate of the neuron can
change and there can be an increase in the coherence between spikes and the
local field potential in the gamma-frequency range (30-50 Hz). The hypothesis
explored here is that these observed effects of attention could be a
consequence of changes in the synchrony of local interneuron networks. We
performed computer simulations of a Hodgkin-Huxley type neuron driven by a
constant depolarizing current, I, representing visual stimulation and a
modulatory inhibitory input representing the effects of attention via local
interneuron networks. We observed that the neuron's firing rate and the
coherence of its output spike train with the synaptic inputs was modulated by
the degree of synchrony of the inhibitory inputs. The model suggest that the
observed changes in firing rate and coherence of neurons in the visual cortex
could be controlled by top-down inputs that regulated the coherence in the
activity of a local inhibitory network discharging at gamma frequencies.Comment: J.Physiology (Paris) in press, 11 figure
State Dependence of Stimulus-Induced Variability Tuning in Macaque MT
Behavioral states marked by varying levels of arousal and attention modulate
some properties of cortical responses (e.g. average firing rates or pairwise
correlations), yet it is not fully understood what drives these response
changes and how they might affect downstream stimulus decoding. Here we show
that changes in state modulate the tuning of response variance-to-mean ratios
(Fano factors) in a fashion that is neither predicted by a Poisson spiking
model nor changes in the mean firing rate, with a substantial effect on
stimulus discriminability. We recorded motion-sensitive neurons in middle
temporal cortex (MT) in two states: alert fixation and light, opioid
anesthesia. Anesthesia tended to lower average spike counts, without decreasing
trial-to-trial variability compared to the alert state. Under anesthesia,
within-trial fluctuations in excitability were correlated over longer time
scales compared to the alert state, creating supra-Poisson Fano factors. In
contrast, alert-state MT neurons have higher mean firing rates and largely
sub-Poisson variability that is stimulus-dependent and cannot be explained by
firing rate differences alone. The absence of such stimulus-induced variability
tuning in the anesthetized state suggests different sources of variability
between states. A simple model explains state-dependent shifts in the
distribution of observed Fano factors via a suppression in the variance of gain
fluctuations in the alert state. A population model with stimulus-induced
variability tuning and behaviorally constrained information-limiting
correlations explores the potential enhancement in stimulus discriminability by
the cortical population in the alert state.Comment: 36 pages, 18 figure
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