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1.
Networks of synchronized fast-spiking interneurons are thought to be key elements in the generation of gamma (γ) oscillations
(30–80 Hz) in the brain. We examined how such γ-oscillatory inhibition regulates the output of a cortical pyramidal cell.
Specifically, we modeled a situation where a pyramidal cell receives inputs from γ-synchronized fast-spiking inhibitory interneurons.
This model successfully reproduced several important aspects of a recent experimental result regarding the γ-inhibitory regulation
of pyramidal cellular firing that is presumably associated with the sensation of whisker stimuli. Through an in-depth analysis
of this model system, we show that there is an obvious rhythmic gating effect of the γ-oscillated interneuron networks on
the pyramidal neuron’s signal transmission. This effect is further illustrated by the interactions of this interneuron network
and the pyramidal neuron. Prominent power in the γ frequency range can emerge provided that there are appropriate delays on
the excitatory connections and inhibitory synaptic conductance between interneurons. These results indicate that interactions
between excitation and inhibition are critical for the modulation of coherence and oscillation frequency of network activities. 相似文献
2.
The brain exhibits temporally complex patterns of activity with features similar to those of chaotic systems. Theoretical studies over the last twenty years have described various computational advantages for such regimes in neuronal systems. Nevertheless, it still remains unclear whether chaos requires specific cellular properties or network architectures, or whether it is a generic property of neuronal circuits. We investigate the dynamics of networks of excitatory-inhibitory (EI) spiking neurons with random sparse connectivity operating in the regime of balance of excitation and inhibition. Combining Dynamical Mean-Field Theory with numerical simulations, we show that chaotic, asynchronous firing rate fluctuations emerge generically for sufficiently strong synapses. Two different mechanisms can lead to these chaotic fluctuations. One mechanism relies on slow I-I inhibition which gives rise to slow subthreshold voltage and rate fluctuations. The decorrelation time of these fluctuations is proportional to the time constant of the inhibition. The second mechanism relies on the recurrent E-I-E feedback loop. It requires slow excitation but the inhibition can be fast. In the corresponding dynamical regime all neurons exhibit rate fluctuations on the time scale of the excitation. Another feature of this regime is that the population-averaged firing rate is substantially smaller in the excitatory population than in the inhibitory population. This is not necessarily the case in the I-I mechanism. Finally, we discuss the neurophysiological and computational significance of our results. 相似文献
3.
It has been suggested that excitatory and inhibitory inputs to cortical cells are balanced, and that this balance is important for the highly irregular firing observed in the cortex. There are two hypotheses as to the origin of this balance. One assumes that it results from a stable solution of the recurrent neuronal dynamics. This model can account for a balance of steady state excitation and inhibition without fine tuning of parameters, but not for transient inputs. The second hypothesis suggests that the feed forward excitatory and inhibitory inputs to a postsynaptic cell are already balanced. This latter hypothesis thus does account for the balance of transient inputs. However, it remains unclear what mechanism underlies the fine tuning required for balancing feed forward excitatory and inhibitory inputs. Here we investigated whether inhibitory synaptic plasticity is responsible for the balance of transient feed forward excitation and inhibition. We address this issue in the framework of a model characterizing the stochastic dynamics of temporally anti-symmetric Hebbian spike timing dependent plasticity of feed forward excitatory and inhibitory synaptic inputs to a single post-synaptic cell. Our analysis shows that inhibitory Hebbian plasticity generates 'negative feedback' that balances excitation and inhibition, which contrasts with the 'positive feedback' of excitatory Hebbian synaptic plasticity. As a result, this balance may increase the sensitivity of the learning dynamics to the correlation structure of the excitatory inputs. 相似文献
4.
Understanding of how neurons transform fluctuations of membrane potential, reflecting input activity, into spike responses, which communicate the ultimate results of single-neuron computation, is one of the central challenges for cellular and computational neuroscience. To study this transformation under controlled conditions, previous work has used a signal immersed in noise paradigm where neurons are injected with a current consisting of fluctuating noise that mimics on-going synaptic activity and a systematic signal whose transmission is studied. One limitation of this established paradigm is that it is designed to examine the encoding of only one signal under a specific, repeated condition. As a result, characterizing how encoding depends on neuronal properties, signal parameters, and the interaction of multiple inputs is cumbersome. Here we introduce a novel fully-defined signal mixture paradigm, which allows us to overcome these problems. In this paradigm, current for injection is synthetized as a sum of artificial postsynaptic currents (PSCs) resulting from the activity of a large population of model presynaptic neurons. PSCs from any presynaptic neuron(s) can be now considered as “signal”, while the sum of all other inputs is considered as “noise”. This allows us to study the encoding of a large number of different signals in a single experiment, thus dramatically increasing the throughput of data acquisition. Using this novel paradigm, we characterize the detection of excitatory and inhibitory PSCs from neuronal spike responses over a wide range of amplitudes and firing-rates. We show, that for moderately-sized neuronal populations the detectability of individual inputs is higher for excitatory than for inhibitory inputs during the 2–5 ms following PSC onset, but becomes comparable after 7–8 ms. This transient imbalance of sensitivity in favor of excitation may enhance propagation of balanced signals through neuronal networks. Finally, we discuss several open questions that this novel high-throughput paradigm may address. 相似文献
5.
Recent physiological studies have shown that neurons in various regions of the central nervous systems continuously receive noisy excitatory and inhibitory synaptic inputs in a balanced and covaried fashion. While this balanced synaptic input (BSI) is typically described in terms of maintaining the stability of neural circuits, a number of experimental and theoretical studies have suggested that BSI plays a proactive role in brain functions such as top-down modulation for executive control. Two issues have remained unclear in this picture. First, given the noisy nature of neuronal activities in neural circuits, how do the modulatory effects change if the top-down control implements BSI with different ratios between inhibition and excitation? Second, how is a top-down BSI realized via only excitatory long-range projections in the neocortex? To address the first issue, we systematically tested how the inhibition/excitation ratio affects the accuracy and reaction times of a spiking neural circuit model of perceptual decision. We defined an energy function to characterize the network dynamics, and found that different ratios modulate the energy function of the circuit differently and form two distinct functional modes. To address the second issue, we tested BSI with long-distance projection to inhibitory neurons that are either feedforward or feedback, depending on whether these inhibitory neurons do or do not receive inputs from local excitatory cells, respectively. We found that BSI occurs in both cases. Furthermore, when relying on feedback inhibitory neurons, through the recurrent interactions inside the circuit, BSI dynamically and automatically speeds up the decision by gradually reducing its inhibitory component in the course of a trial when a decision process takes too long. 相似文献
6.
We consider the effects of temporal delay in a neural feedback system with excitation and inhibition. The topology of our model system reflects the anatomy of the avian isthmic circuitry, a feedback structure found in all classes of vertebrates. We show that the system is capable of performing a 'winner-take-all' selection rule for certain combinations of excitatory and inhibitory feedback. In particular, we show that when the time delays are sufficiently large a system with local inhibition and global excitation can function as a 'winner-take-all' network and exhibit oscillatory dynamics. We demonstrate how the origin of the oscillations can be attributed to the finite delays through a linear stability analysis. 相似文献
7.
Carl Van Vreeswijk L. F. Abbott G. Bard Ermentrout 《Journal of computational neuroscience》1994,1(4):313-321
Excitatory and inhibitory synaptic coupling can have counter-intuitive effects on the synchronization of neuronal firing. While it might appear that excitatory coupling would lead to synchronization, we show that frequently inhibition rather than excitation synchronizes firing. We study two identical neurons described by integrate-and-fire models, general phase-coupled models or the Hodgkin-Huxley model with mutual, non-instantaneous excitatory or inhibitory synapses between them. We find that if the rise time of the synapse is longer than the duration of an action potential, inhibition not excitation leads to synchronized firing. 相似文献
8.
The development of synchronous bursting in neuronal ensembles represents an important change in network behavior. To determine
the influences on development of such synchronous bursting behavior we study the dynamics of small networks of sparsely connected
excitatory and inhibitory neurons using numerical simulations. The synchronized bursting activities in networks evoked by
background spikes are investigated. Specifically, patterns of bursting activity are examined when the balance between excitation
and inhibition on neuronal inputs is varied and the fraction of inhibitory neurons in the network is changed. For quantitative
comparison of bursting activities in networks, measures of the degree of synchrony are used. We demonstrate how changes in
the strength of excitation on inputs of neurons can be compensated by changes in the strength of inhibition without changing
the degree of synchrony in the network. The effects of changing several network parameters on the network activity are analyzed
and discussed. These changes may underlie the transition of network activity from normal to potentially pathologic (e.g.,
epileptic) states.
Received: 21 May 2002 / Accepted in revised form: 3 December 2002 / Published online: 7 March 2003
Correspondence to: P. Kudela (e-mail: pkudela@jhmi.edu)
Acknowledgements. This research was supported by NIH grant NS 38958. 相似文献
9.
Michael J. Hull Stephen R. Soffe David J. Willshaw Alan Roberts 《PLoS computational biology》2016,12(1)
What cellular and network properties allow reliable neuronal rhythm generation or firing that can be started and stopped by brief synaptic inputs? We investigate rhythmic activity in an electrically-coupled population of brainstem neurons driving swimming locomotion in young frog tadpoles, and how activity is switched on and off by brief sensory stimulation. We build a computational model of 30 electrically-coupled conditional pacemaker neurons on one side of the tadpole hindbrain and spinal cord. Based on experimental estimates for neuron properties, population sizes, synapse strengths and connections, we show that: long-lasting, mutual, glutamatergic excitation between the neurons allows the network to sustain rhythmic pacemaker firing at swimming frequencies following brief synaptic excitation; activity persists but rhythm breaks down without electrical coupling; NMDA voltage-dependency doubles the range of synaptic feedback strengths generating sustained rhythm. The network can be switched on and off at short latency by brief synaptic excitation and inhibition. We demonstrate that a population of generic Hodgkin-Huxley type neurons coupled by glutamatergic excitatory feedback can generate sustained asynchronous firing switched on and off synaptically. We conclude that networks of neurons with NMDAR mediated feedback excitation can generate self-sustained activity following brief synaptic excitation. The frequency of activity is limited by the kinetics of the neuron membrane channels and can be stopped by brief inhibitory input. Network activity can be rhythmic at lower frequencies if the neurons are electrically coupled. Our key finding is that excitatory synaptic feedback within a population of neurons can produce switchable, stable, sustained firing without synaptic inhibition. 相似文献
10.
Acoustic signals transmit information by temporal characteristics and envelope periodicity as well as by their frequency content.
Many animals can extract the frequency content of a signal by means of specialized organs such as the cochlea but for the
detection and identification of higher-order periodicity, e.g., amplitude modulations, this type of organ is useless. In addition,
many animals do not have a cochlea but still depend on a reliable identification of different frequencies in the vast variety
of acoustic signals they perceive in their natural environment. Hence, neural mechanisms to decode periodicity information
must exist. We present a detailed mathematical analysis of a recurrent and a feedforward model of neuronal periodicity extraction
and discuss basic constraints for neuronal circuitry performing such a task in a biological system. Both the recurrent and
the feedforward model perform well using neuronal parameters typical for the auditory system. Performance is limited mainly
by the temporal precision of the connections between the neurons. 相似文献
11.
Based on anatomical and physiological data pertaining to severalmoth species and the cockroach, we propose a neural model forpheromone discrimination in the insect antennal lobe. The modelexploits the variety of neuronal response patterns observedin the macroglomerulus, and predicts how these complex patternsof excitation and inhibition can participate in the discriminationof the species-specific pheromone blend. The model also allowsus to investigate the relationship between the distributionof observed response patterns and the neural organization fromwhich these patterns emerge. Chem. Senses 21: 1927, 1996. 相似文献
12.
Neuronal avalanches are a form of spontaneous activity widely observed in cortical slices and other types of nervous tissue, both in vivo and in vitro. They are characterized by irregular, isolated population bursts when many neurons fire together, where the number of spikes per burst obeys a power law distribution. We simulate, using the Gillespie algorithm, a model of neuronal avalanches based on stochastic single neurons. The network consists of excitatory and inhibitory neurons, first with all-to-all connectivity and later with random sparse connectivity. Analyzing our model using the system size expansion, we show that the model obeys the standard Wilson-Cowan equations for large network sizes ( neurons). When excitation and inhibition are closely balanced, networks of thousands of neurons exhibit irregular synchronous activity, including the characteristic power law distribution of avalanche size. We show that these avalanches are due to the balanced network having weakly stable functionally feedforward dynamics, which amplifies some small fluctuations into the large population bursts. Balanced networks are thought to underlie a variety of observed network behaviours and have useful computational properties, such as responding quickly to changes in input. Thus, the appearance of avalanches in such functionally feedforward networks indicates that avalanches may be a simple consequence of a widely present network structure, when neuron dynamics are noisy. An important implication is that a network need not be “critical” for the production of avalanches, so experimentally observed power laws in burst size may be a signature of noisy functionally feedforward structure rather than of, for example, self-organized criticality. 相似文献
13.
We present a functional model of the cerebellum comprising cerebellar cortex, inferior olive, deep cerebellar nuclei, and
brain stem nuclei. The discerning feature of the model being time coding, we consistently describe the system in terms of
postsynaptic potentials, synchronous action potentials, and propagation delays. We show by means of detailed single-neuron
modeling that (i) Golgi cells can fulfill a gating task in that they form short and well-defined time windows within which
granule cells can reach firing threshold, thus organizing neuronal activity in discrete `time slices', and that (ii) rebound
firing in cerebellar nuclei cells is a robust mechanism leading to a delayed reverberation of Purkinje cell activity through
cerebellar-reticular projections back to the cerebellar cortex. Computer simulations of the whole cerebellar network consisting
of several thousand neurons reveal that reverberation in conjunction with long-term plasticity at the parallel fiber-Purkinje
cell synapses enables the system to learn, store, and recall spatio-temporal patterns of neuronal activity. Climbing fiber
spikes act both as a synchronization and as a teacher signal, not as an error signal. They are due to intrinsic oscillatory
properties of inferior olivary neurons and to delayed reverberation within the network. In addition to clear experimental
predictions the present theory sheds new light on a number of experimental observation such as the synchronicity of climbing
fiber spikes and provides a novel explanation of how the cerebellum solves timing tasks on a time scale of several hundreds
of milliseconds.
Received: 23 July 1999 / Accepted in revised form: 31 August 1999 相似文献
14.
A recent computational study of gain control via shunting inhibition has shown that the slope of the frequency-versus-input (f-I) characteristic of a neuron can be decreased by increasing the noise associated with the inhibitory input (Neural Comput. 13, 227-248). This novel noise-induced divisive gain control relies on the concommittant increase of the noise variance with the mean of the total inhibitory conductance. Here we investigate this effect using different neuronal models. The effect is shown to occur in the standard leaky integrate-and-fire (LIF) model with additive Gaussian white noise, and in the LIF with multiplicative noise acting on the inhibitory conductance. The noisy scaling of input currents is also shown to occur in the one-dimensional theta-neuron model, which has firing dynamics, as well as a large scale compartmental model of a pyramidal cell in the electrosensory lateral line lobe of a weakly electric fish. In this latter case, both the inhibition and the excitatory input have Poisson statistics; noise-induced divisive inhibition is thus seen in f-I curves for which the noise increases along with the input I. We discuss how the variation of the noise intensity along with inputs is constrained by the physiological context and the class of model used, and further provide a comparison of the divisive effect across models. 相似文献
15.
Since the discovery of the major excitatory and inhibitory neurotransmitters and their receptors in the brain, many have deliberated over their likely structures and how these may relate to function. This was initially satisfied by the determination of the first amino acid sequences of the Cys-loop receptors that recognized acetylcholine, serotonin, GABA, and glycine, followed later by similar determinations for the glutamate receptors, comprising non-NMDA and NMDA subtypes. The last decade has seen a rapid advance resulting in the first structures of Cys-loop receptors, related bacterial and molluscan homologs, and glutamate receptors, determined down to atomic resolution. This now provides a basis for determining not just the complete structures of these important receptor classes, but also for understanding how various domains and residues interact during agonist binding, receptor activation, and channel opening, including allosteric modulation. This article reviews our current understanding of these mechanisms for the Cys-loop and glutamate receptor families.To understand how neurons communicate with each other requires a fundamental understanding of neurotransmitter receptor structure and function. Neurotransmitter-gated ion channels, also known as ionotropic receptors, are responsible for fast synaptic transmission. They decode chemical signals into electrical responses, thereby transmitting information from one neuron to another. Their suitability for this important task relies on their ability to respond very rapidly to the transient release of neurotransmitter to affect cell excitability.In the central nervous system (CNS), fast synaptic transmission results in two main effects: neuronal excitation and inhibition. For excitation, the principal neurotransmitter involved is glutamate, which interacts with ionotropic (integral ion channel) and metabotropic (second-messenger signaling) receptors. The ionotropic glutamate receptors are permeable to cations, which directly cause excitation. Acetylcholine and serotonin can also activate specific cation-selective ionotropic receptors to affect neuronal excitation. For controlling cell excitability, inhibition is important, and this is mediated by the neurotransmitters GABA and glycine, causing an increased flux of anions. GABA predominates as the major inhibitory transmitter throughout the CNS, whereas glycine is of greater importance in the spinal cord and brainstem. They both activate specific receptors—for GABA, there are ionotropic and metabotropic receptors, whereas for glycine, only ionotropic receptors are known to date.Together with acetylcholine- and serotonin-gated channels, GABA and glycine ionotropic receptors form the superfamily of Cys-loop receptors, which differs in many aspects from the superfamily of ionotropic glutamate receptors. Over the last two decades, our knowledge of the structure and function of ionotropic receptors has grown rapidly. In this article, we summarize our current understanding of the molecular operation of these receptors and how we can now begin to interpret the role of receptor structure in agonist binding, channel activation, and allosteric modulation of Cys-loop and glutamate receptor families. Further details on the regulation and trafficking of neurotransmitter receptors in synaptic structure and plasticity can be found in accompanying articles. 相似文献
16.
The balance between inhibition and excitation plays a crucial role in the generation of synchronous bursting activity in neuronal circuits. In human and animal models of epilepsy, changes in both excitatory and inhibitory synaptic inputs are known to occur. Locations and distribution of these excitatory and inhibitory synaptic inputs on pyramidal cells play a role in the integrative properties of neuronal activity, e.g., epileptiform activity. Thus the location and distribution of the inputs onto pyramidal cells are important parameters that influence neuronal activity in epilepsy. However, the location and distribution of inhibitory synapses converging onto pyramidal cells have not been fully studied. The objectives of this study are to investigate the roles of the relative location of inhibitory synapses on the dendritic tree and soma in the generation of bursting activity. We investigate influences of somatic and dendritic inhibition on bursting activity patterns in several paradigms of potential connections using a simplified multicompartmental model. We also investigate the effects of distribution of fast and slow components of GABAergic inhibition in pyramidal cells. Interspike interval (ISI) analysis is used for examination of bursting patterns. Simulations show that the inhibitory interneuron regulates neuronal bursting activity. Bursting behavior patterns depend on the synaptic weight and delay of the inhibitory connection as well as the location of the synapse. When the inhibitory interneuron synapses on the pyramidal neuron, inhibitory action is stronger if the inhibitory synapse is close to the soma. Alterations of synaptic weight of the interneuron can be compensatory for changes in the location of synaptic input. The relative changes in these parameters exert a considerable influence on whether synchronous bursting activity is facilitated or reduced. Additional simulations show that the slow GABAergic inhibitory component is more effective than the fast component in distal dendrites. Taken together, these findings illustrate the potential for GABAergic inhibition in the soma and dendritic tree to play an important modulatory role in bursting activity patterns. 相似文献
17.
Recently Haas et al. (J Neurophysiol 96: 3305–3313, 2006), observed a novel form of spike timing dependent plasticity (iSTDP) in GABAergic synaptic couplings in layer II of the entorhinal
cortex. Depending on the relative timings of the presynaptic input at time t
pre and the postsynaptic excitation at time t
post, the synapse is strengthened (Δt = t
post − t
pre > 0) or weakened (Δt < 0). The temporal dynamic range of the observed STDP rule was found to lie in the higher gamma frequency band (≥40 Hz),
a frequency range important for several vital neuronal tasks. In this paper we study the function of this novel form of iSTDP
in the synchronization of the inhibitory neuronal network. In particular we consider a network of two unidirectionally coupled
interneurons (UCI) and two mutually coupled interneurons (MCI), in the presence of heterogeneity in the intrinsic firing rates
of each coupled neuron. Using the method of spike time response curve (STRC), we show how iSTDP influences the dynamics of
the coupled neurons, such that the pair synchronizes under moderately large heterogeneity in the firing rates. Using the general
properties of the STRC for a Type-1 neuron model (Ermentrout, Neural Comput 8:979–1001, 1996) and the observed iSTDP we determine conditions on the initial configuration of the UCI network that would result in 1:1
in-phase synchrony between the two coupled neurons. We then demonstrate a similar enhancement of synchrony in the MCI with
dynamic synaptic modulation. For the MCI we also consider heterogeneity introduced in the network through the synaptic parameters:
the synaptic decay time of mutual inhibition and the self inhibition synaptic strength. We show that the MCI exhibits enhanced
synchrony in the presence of all the above mentioned sources of heterogeneity and the mechanism for this enhanced synchrony
is similar to the case of the UCI. 相似文献
18.
19.
Jens Kremkow Laurent U. Perrinet Guillaume S. Masson Ad Aertsen 《Journal of computational neuroscience》2010,28(3):579-594
Neurons in the neocortex receive a large number of excitatory and inhibitory synaptic inputs. Excitation and inhibition dynamically
balance each other, with inhibition lagging excitation by only few milliseconds. To characterize the functional consequences
of such correlated excitation and inhibition, we studied models in which this correlation structure is induced by feedforward
inhibition (FFI). Simple circuits show that an effective FFI changes the integrative behavior of neurons such that only synchronous
inputs can elicit spikes, causing the responses to be sparse and precise. Further, effective FFI increases the selectivity
for propagation of synchrony through a feedforward network, thereby increasing the stability to background activity. Last,
we show that recurrent random networks with effective inhibition are more likely to exhibit dynamical network activity states
as have been observed in vivo. Thus, when a feedforward signal path is embedded in such recurrent network, the stabilizing effect of effective inhibition
creates an suitable substrate for signal propagation. In conclusion, correlated excitation and inhibition support the notion
that synchronous spiking may be important for cortical processing. 相似文献
20.
Neurons in the insect antennal lobe represent odors as spatiotemporal patterns of activity that unfold over multiple time scales. As these patterns unspool they decrease the overlap between odor representations and thereby increase the ability of the olfactory system to discriminate odors. Using a realistic model of the insect antennal lobe we examined two competing components of this process -lateral excitation from local excitatory interneurons, and slow inhibition from local inhibitory interneurons. We found that lateral excitation amplified differences between representations of similar odors by recruiting projection neurons that did not receive direct input from olfactory receptors. However, this increased sensitivity also amplified noisy variations in input and compromised the ability of the system to respond reliably to multiple presentations of the same odor. Slow inhibition curtailed the spread of projection neuron activity and increased response reliability. These competing influences must be finely balanced in order to decorrelate odor representations. 相似文献