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Biomedical subjects

P Y Burgi

Publications and source records attributed to P Y Burgi.

5 recordsLinked to original sources

Probabilistic motion estimation based on temporal coherence.

We develop a theory for the temporal integration of visual motion motivated by psychophysical experiments. The theory proposes that input data are temporally grouped and used to predict and estimate the motion flows in the image sequence. This temporal grouping can be considered a generalization of the data association techniques that engineers use to study motion sequences. Our temporal grouping theory is expressed in terms of the Bayesian generalization of standard Kalman filtering. To implement the theory, we derive a parallel network that shares some properties of cortical networks. Computer simulations of this network demonstrate that our theory qualitatively accounts for psychophysical experiments on motion occlusion and motion outliers. In deriving our theory, we assumed spatial factorizability of the probability distributions and made the approximation of updating the marginal distributions of velocity at each point. This allowed us to perform local computations and simplified our implementation. We argue that these approximations are suitable for the stimuli we are considering (for which spatial coherence effects are negligible).

Bayes Theorem↗

Toward a biophysically plausible bidirectional Hebbian rule.

Although the commonly used quadratic Hebbian-anti-Hebbian rules lead to successful models of plasticity and learning, they are inconsistent with neurophysiology. Other rules, more physiologically plausible, fail to specify the biological mechanism of bidirectionality and the biological mechanism that prevents synapses from changing from excitatory to inhibitory, and vice versa. We developed a synaptic bidirectional Hebbian rule that does not suffer from these problems. This rule was compared with physiological homosynaptic conditions in the hippocampus, with the results indicating the consistency of this rule with long-term potentiation (LTP) and long-term depression (LTD) phenomenologies. The phenomenologies considered included the reversible dynamics of LTP and LTD and the effects of N-methyl-D-aspartate blockers and phosphatase inhibitors.

Biophysical Phenomena↗

A biophysical model for the developmental time course of retinal orientation selectivity.

A quantitative study of the time course of development of the percentage of orientationally selective and isotropic ganglion cells in turtle retina has recently been performed. This study revealed that as soon as ganglion cells start responding to light, a large percentage of them are selective to the orientations of moving visual stimuli. This percentage decreases with age to reach a minimum around hatching, increases dramatically after birth and finally, decreases again following the first month of life to reach adult level. Concomitantly, the percentage of cells responding isotropically to the orientation of elongated stimuli increases monotonically until about 30 days after birth, stabilizing afterwards. To account for both time courses, we propose a biophysical model implementing features ubiquitous to developing vertebrate retinas. These features include early dendritic and synaptic spatial polarization, dendritic growth, and waves of activity generated spontaneously or by visual stimulation sweeping across the inner plexiform layer (IPL). The model also assumes a physiologically plausible Hebbian rule, which includes long-term potentiation and depression. Computer simulations of this model yield good fits of the data. The quality of these fits confirms and extends results from an earlier model using computationally-simple mechanisms, which suggested that early dendritic polarization might be the seed for mature orientation selectivity.

Animals↗

Possible roles of spontaneous waves and dendritic growth for retinal receptive field development.

Several models of cortical development postulate that a Hebbian process fed by spontaneous activity amplifies orientation biases occurring randomly in early wiring, to form orientation selectivity. These models are not applicable to the development of retinal orientation selectivity, since they neglect the polarization of the retina's poorly branched early dendritic trees and the wavelike organization of the retina's early noise. There is now evidence that dendritic polarization and spontaneous waves are key in the development of retinal receptive fields. When models of cortical development are modified to take these factors into account, one obtains a model of retinal development in which early dendritic polarization is the seed of orientation selectivity, while the spatial extent of spontaneous waves controls the spatial profile of receptive fields and their tendency to be isotropic.

Dendrites↗

Model for the pharmacological basis of spontaneous synchronous activity in developing retinas.

Spontaneous waves of bursts of action potentials propagate across the ganglion-cell surface of developing retinas. A recent biophysical model postulated that this propagation is mediated by an increase in extracellular K+, following its ejection from ganglion cells during action potentials. Moreover, the model hypothesized that bursts might terminate due to the accumulation of intracellular Ca2+ and the subsequent activation of a Ca(2+)-dependent K+ conductance in the cells' dendrites. Finally, the model proposed that an excitatory synaptic drive causes a neuromodulation of the waves' properties. To test the feasibility of the model, we performed computer simulations of the network of developing ganglion cells under control and pharmacological-manipulation conditions. In particular, we simulated the effects of neostigmine, Cs+ and TEA, low Ca2+ concentrations, and Co2+. A comparison of the simulations with electrophysiological and pharmacological experimental data recently obtained in turtles (Sernagor and Grzywacz, 1993a), and cats and ferrets (Meister et al., 1991; Wong et al., 1993), showed that the model for the most part is consistent with the behavior of developing retinas. Moreover, modifications of the model to allow for GABAergic inputs onto ganglion cells (Sernagor and Grzywacz, 1994) and poor [K+]out buffering (Connors et al., 1982) improved the model's fits. These results lent further support to important roles of extracellular K+ concentration and synaptic drive for the propagation of waves.

Aging↗