We developed a biologically inspired neural network model of the human primary visual system, consisting of two retinas, two layers of dorso-lateral geniculate nucleus and section B and C of layer 4 of the primary visual cortex. The model was built using GENESIS (www.genesis-sim.org) and comprises about 150,000 neurons. Three different kinds of neurons were incorporated, namely thalamic relay neurons, and excitatory and inhibitory cortical neurons. The processing of input in the retina was simply modeled as random-spike units, where the average firing rate corresponds to the input intensity. The neurons consisted of a soma, an axon and two or four dendrites for relay or inhibitory and excitatory neurons, respectively. We used different ionic channels to reproduce the desired firing behaviour. Synaptic transmission was implemented using the built-in excitatory and inhibitory synaptic channels.

We designed a protocol to explore the center-surround suppression capabilities of our model. The retina was stimulated with contrast stimuli similar to those used in [2]. We compared activity in central neurons of layer 4B and 4C in response to two stimuli with a focal circle of 40% Michelson contrast, where the target stimulus had a high-contrast surrounding while the reference had a uniform surrounding. We found a decrease in activity of 27.73% in layer 4B and one of 31.41% layer 4C when comparing responses to the target with responses to the reference.

A plausible neural network model of the human primary visual system which is consistent with psychophysical effects previously reported in humans [2] is a starting point to further investigate the role of GABAergic inhibition in visual context integration. The capabilities of the model to explain both individual variance of CSS strength and CSS in pathological conditions of GABAergic neurotransmission remains to be tested. We plan to do so on the basis of psychophysical CSS data in humans and corresponding in vivo measurements of GABA and Glutamate concentrations in primary visual cortex using Proton Magnetic Resonance Spectroscopy (1H-MRS).