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Transmission across neocortical synapses depends on the frequency of presynaptic activity (Thomson & Deuchars 1994). Inter-pyramidal synapses in layer V exhibit fast depression of synaptic transmission while other types of synapses exhibit facilitation of transmission. To study the role of dynamic synapses in network computation, we propose a unified phenomenological model which allows computation of the post-synaptic current generated by both types of synapses when driven by an arbitrary pattern of action potential (AP) activity in a presynaptic population. Using this formalism we analyze different regimes of synaptic transmission and demonstrate that dynamic synapses transmit different aspects of the presynaptic activity depending on the average presynaptic frequency. The model also allows for derivation of mean-field equations which govern the activity of large interconnected networks. We show that dynamics of synaptic transmission results in complex sets of regular and irregular...

The origin of orientation selectivity in visual cortical responses is a central problem for understanding cerebral cortical circuitry. In cats, many experiments suggest that orientation selectivity arises from the arrangement of lateral geniculate nucleus (LGN) afferents to layer 4 simple cells. However, this explanation is not sufficient to account for the contrast invariance of orientation tuning. To understand contrast invariance, we first characterize the input to cat simple cells generated by the oriented arrangement of LGN afferents. We demonstrate that it has two components: a spatial-phase-specific component (i.e., one that depends on receptive field spatial phase), which is tuned for orientation, and a phase-nonspecific component, which is untuned. Both components grow with contrast. Second, we show that a correlation-based intracortical circuit,

This article is published in The Journal of Neuroscience, Rapid

Tufted layer 5 (TL5) pyramidal neurons are important projection neurons from the cerebral cortex to subcortical areas. Recent and ongoing experiments aimed at understanding the computational analysis performed by a network of synaptically connected TL5 neurons are reviewed here. The experiments employed dual and triple whole-cell patch clamp recordings from visually identified and preselected neurons in brain slices of somatosensory cortex of young (14- to 16-day-old) rats. These studies suggest that a local network of TL5 neurons within a cortical module of diameter 300 μm consists of a few hundred neurons that are extensively interconnected with reciprocal feedback from at least first-, second- and third-order target neurons. A statistical analysis of synaptic innervation suggests that this recurrent network is not randomly arranged and hence each neuron could be functionally unique. Synaptic transmission between these neurons is characterized by use-dependent synaptic depression which confers novel properties to this recurrent network of neurons. First, a range of rates of depression for different synaptic connections enable each TL5 neuron to receive a unique mixture of information about the average firing rates and the temporally correlated action potential (AP) activity in the population of presynaptic TL5 neurons. Second, each AP generated by any neuron in the network induces a change (defined as an iteration step) in the functional coupling of the neurons in the network (defined as network configuration). It is proposed that the network configuration is iterated during a stimulus to achieve an optimally orchestrated network response. Hebbian, anti-Hebbian and neuromodulatory-induced modifications of neurotransmitter release probability change the rates of synaptic depression and thereby alter the iteration step size. These data may be important to understand the dynamics of electrical activity within the network.

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In most neural network models, synapses are treated as static weights that change only on the slow time scales of learning. It is well known, however, that synapses are highly dynamic, and show use-dependent plasticity over a wide range of time scales. Moreover, synaptic transmission is an inherently stochastic process: a spike arriving at a presynaptic terminal triggers release of a vesicle of neurotransmitter from a release site with a probability that can be much less than one. We consider

How does a neuron vary its mean output firing rate if the input changes from random to coherent activity? What are the critical parameters of the neuronal dynamics and input statistics? To answer these questions, we investigate the coincidence detection properties of an integrate-and-fire neuron. We derive an expression indicating how coincidence detection depends on neuronal parameters. Specifically, (i) we show how coincidence detection depends on the shape of the postsynaptic response function, the number of synapses, and the input statistics, and (ii) we demonstrate that there is an optimal threshold. Our considerations can be used to predict from neuronal parameters whether and to what extent a neuron can act as a coincidence detector and thus can convert a temporal code into a rate code. Physik-Department der TU Munchen (T35), D-85747 Garching bei Munchen, Germany y Swiss Federal Institute of Technology, Center of Neuromimetic Systems, EPFL-DI, CH-1015 Lausanne, Switz...

Experimental data show that biological synapses behave quite differently from the symbolic synapses in all common artificial neural network models. Biological synapses are

Most experimental and theoretical studies of brain function assume that neurons transmit information as a rate code, but recent studies on the speed of visual processing impose temporal constraints that appear incompatible with such a coding scheme. Other coding schemes that use the pattern of spikes across a population a neurons may be much more efficient. For example, since strongly activated neurons tend to fire first, one can use the order of firing as a code. We argue that Rank Order Coding is not only very efficient, but also easy to implement in biological hardware: neurons can be made sensitive to the order of activation of their inputs by including a feed-forward shunting inhibition mechanism that progressively desensitizes the neuronal population during a wave of afferent activity. In such a case, maximum activation will only be produced when the afferent inputs are activated in the order of their synaptic weights.