The American Psychiatric Association (APA) has updated its Privacy Policy and Terms of Use, including with new information specifically addressed to individuals in the European Economic Area. As described in the Privacy Policy and Terms of Use, this website utilizes cookies, including for the purpose of offering an optimal online experience and services tailored to your preferences.

Please read the entire Privacy Policy and Terms of Use. By closing this message, browsing this website, continuing the navigation, or otherwise continuing to use the APA's websites, you confirm that you understand and accept the terms of the Privacy Policy and Terms of Use, including the utilization of cookies.

×

To the Editor: The retina in all vertebrates is composed of three layers of nerve cell bodies and two layers of synapses. The first area of neuropil, where synaptic contacts occur, is the outer plexiform layer, in which connections between rod and cones, and vertically running bipolar cells and horizontally oriented horizontal cells, occur. 1

Experimental data suggests that some classes of spiking neurons in the first layers of sensory systems are electrically coupled via gap junctions or ephaptic interactions. When the electrical coupling is removed, the response function (firing rate versus stimulus intensity) of the uncoupled neurons typically shows a decrease in dynamic range and sensitivity. 2 In addition, chemical coupling by neurotransmitter release has been seen in the inner plexiform layer of the retina, where amacrine cells, bipolar cells, and ganglion cells have chemical synapses, and it has been shown that amacrine cells play a synchronization role by giving feedback on ganglion cells for generating spontaneous activity in developing vertebrate retina. 3 , 4 In order to simulate this spontaneous behavior, Godfrey and Swindale 3 used deterministic cellular automaton.

Cellular automaton is a discrete model studied in complex systems such as biological systems. It consists of a regular grid of cells, each in one of a finite number of states. The grid can be in any finite number of dimensions. Time is also discrete, and the state of a cell at the present time is a function of the states of a finite number of cells (called its neighborhood) at a previous time. These neighbors are a selection of cells interacting with the specified cell and do not change (though the cell itself may be in its neighborhood, it is not usually considered a neighbor). Every cell has the same rule for updating, based on the values in this neighborhood. Each time the rules are applied to the whole grid (lattice), a new generation is created. 5

On the other hand, in the outer plexiform layer, photoreceptors, horizontal cells, and bipolar cells have synapses. Horizontal cell hyperpolarization generates a feedback signal to the photoreceptors. 6 We previously hypothesized that horizontal cells have a functional role in synchronization of photoreceptors, 7 which leads to bursting activity in bipolar cells. To model such a neuropil, we propose the cellular automaton approach. Each cell of the cellular automaton represents a photoreceptor cell. The horizontal cells, which are responsible for interactions between photoreceptors, may be modeled by neighborhood rules of cellular automaton. To determine the new state of the lattice, we consider the previous state of each cell, other cell interactions on the desired cell, and the logarithm of input light intensity. Finally, we let the model evolve.

By proposing such a modeling approach, the horizontal cell role in transferring data from the outer plexiform layer to the inner plexiform layer may be elucidated explicitly. Moreover, we will be able to investigate precisely “off-on” pathways and disease states, which result in decreasing the “a-wave” amplitude and increasing its latency. By defining such a model, we may achieve a more profitable definition of electrical behavior of the outer plexiform layer, which emerged in an a-wave pattern that is important in clinical trials.

Biomedical Engineering Faculty, Amirkabir University of Technology, Tehran, Iran
References

1. Klug K, Herr S, Ngo IT: Macaque retina contains an S-cone OFF midget pathway. J Neurosci 2003; 23:9881–9887Google Scholar

2. Furtado LS, Copelli M: Response of electrically coupled spiking neurons: a cellular automaton approach. Phys Rev E Stat Nonlin Soft Matter Phys 2006; 73:011907Google Scholar

3. Godfrey KB, Swindale NV: Retinal wave behavior through activity-dependent refractory periods. PLoS Comput Biol 2007; 3:e245Google Scholar

4. Feng Y, Yu X, Sun L: Synchronization of uncertain chaotic systems using a single transmission channel. Chaos Solitons Fractals 2008; 35:755–762Google Scholar

5. Morita K: Reversible computing and cellular automata: a survey. Theor Comp Sci 2008; 395:101–131Google Scholar

6. Fahrenfort I, Klooster J, Sjoerdsma T, et al: The involvement of glutamate-gated channels in negative feedback from horizontal cells to cones. Prog Brain Res 2005; 147:219–229Google Scholar

7. Razjouyan J, Fallah A, Gharibzadeh S: Organizational role of retina horizontal cell. J Neuropsychiatry Clin Neurosci 2009; 21:479–480Google Scholar