Simulation of visual processing in retinal ganglion cells

Watson, Michael and Holmes, Graham and Byrne, Terry and Cornford, Stuart (2005) Simulation of visual processing in retinal ganglion cells. In: AuPS/ASB Canberra 2005 Meeting, 27-30 Sep 2005, Canberra, Australia.

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Abstract

The retina contains photoreceptors for light detection as well as Bipolar, Horizontal, Amacrine and Ganglion cells. These form a neural network where synaptic convergence, divergence and integration take place. It serves as a simple network to simulate and thus can be used as a learning tool to demonstrate neural processing, desensitization, experimental design and protocol. The simulation is designed for students to facilitate inquiry based learning. A given retinal ganglion cell responds to light directed to a specific area of the retina. This area is called the ‘receptive field’. Ganglion cell receptive fields have a ‘centre’ and an antagonistic ‘surround’ and can be classified as ‘On Centre’ or ‘Off Centre’. On Centre are activated by light in the centre of the receptive field and inhibited by light in the surrounding receptive field. Off Centre are inhibited by light in the centre of the receptive field and activated by light in the surrounding receptive field The model simulates the receptive fields of four ganglion cells. The four receptive fields are arranged into 4 arrays with each array containing 64 Light Dependent Resistors (LDR’s; EG&G Vactec). These simulate the photoreceptors contained within each receptive field. The LDR’s are connected via the Multiplexor (Temic) and through the programming of a HC12 microprocessor (Motorolla) simulate the ‘On Centre’ and ‘Off Centre’ receptive fields. Students shine a variable point of light onto one of the four array’s and will see either an increase or decrease in the clock rate output of the HC12. This represents a change in the discharge of the ganglion cell. The clock rate output of the HC12 is visualised by means of an oscilloscope. The clock rate output will vary depending on whether they are activating ‘On’ or ‘Off’ LDR’s. Prolonged stimulation of the LDR’s reduces the clock rate output to pre-stimulus levels to simulate desensitization. Students are required to design an experimental protocol that determines an optimal standard stimulus, a systematic protocol for testing the different receptive fields and a protocol for gathering and analysing the data. The simulation challenges students to determine (i) the optimum size, strength and duration of a stimulus that is sufficient to stimulate the receptive field (ii) the receptive field characteristics of retinal ganglion cells (iii) how such receptive fields can be formed on the basis of the cell types and connections found in the retina.


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Item Type: Conference or Workshop Item (Commonwealth Reporting Category E) (Paper)
Refereed: Yes
Item Status: Live Archive
Additional Information: Conference publication consists of only the abstracts of papers presented at the conference. Abstract only posted here.
Depositing User: epEditor USQ
Faculty / Department / School: Historic - Faculty of Sciences - Department of Biological and Physical Sciences
Date Deposited: 11 Oct 2007 00:29
Last Modified: 02 Jul 2013 22:34
Uncontrolled Keywords: retina, retinal ganglion cells, simulation, visual preocessing
Fields of Research (FOR2008): 11 Medical and Health Sciences > 1113 Ophthalmology and Optometry > 111303 Vision Science
11 Medical and Health Sciences > 1113 Ophthalmology and Optometry > 111302 Optical Technology
URI: http://eprints.usq.edu.au/id/eprint/817

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