RESUMEN
Recent studies have shown that local cortical feedback can have an important effect on the response of neurons in primary visual cortex to the orientation of visual stimuli. In this work, we study the role of the cortical feedback in shaping the spatiotemporal patterns of activity in cortex. Two questions are addressed: one, what are the limitations on the ability of cortical neurons to lock their activity to rotating oriented stimuli within a single receptive field? Two, can the local architecture of visual cortex lead to the generation of spontaneous traveling pulses of activity? We study these issues analytically by a population-dynamic model of a hypercolumn in visual cortex. The order parameter that describes the macroscopic behavior of the network is the time-dependent population vector of the network. We first study the network dynamics under the influence of a weakly tuned input that slowly rotates within the receptive field. We show that if the cortical interactions have strong spatial modulation, the network generates a sharply tuned activity profile that propagates across the hypercolumn in a path that is completely locked to the stimulus rotation. The resultant rotating population vector maintains a constant angular lag relative to the stimulus, the magnitude of which grows with the stimulus rotation frequency. Beyond a critical frequency the population vector does not lock to the stimulus but executes a queasi-periodic motion with an average frequency that is smaller than that of the stimulus. In the second part we consider the stable intrinsic state of the cortex under the influence of isotropic stimulation. We show that if the local inhibitory feedback is sufficiently strong, the network does not settle into a stationary state but develops spontaneous traveling pulses of activity. Unlike recent models of wave propagation in cortical networks, the connectivity pattern in our model is spatially symmetric, hence the direction of propagation of these waves is arbitrary. The interaction of these waves with an external-oriented stimulus is studied. It is shown that the system can lock to a weakly tuned rotating stimulus if the stimulus frequency is close to the frequency of the intrinsic wave.
Asunto(s)
Modelos Neurológicos , Red Nerviosa/fisiología , Neuronas/fisiología , Corteza Visual/fisiología , Animales , Simulación por Computador , Retroalimentación , Modelos Teóricos , OrientaciónRESUMEN
The role of intrinsic cortical connections in processing sensory input and in generating behavioral output is poorly understood. We have examined this issue in the context of the tuning of neuronal responses in cortex to the orientation of a visual stimulus. We analytically study a simple network model that incorporates both orientation-selective input from the lateral geniculate nucleus and orientation-specific cortical interactions. Depending on the model parameters, the network exhibits orientation selectivity that originates from within the cortex, by a symmetry-breaking mechanism. In this case, the width of the orientation tuning can be sharp even if the lateral geniculate nucleus inputs are only weakly anisotropic. By using our model, several experimental consequences of this cortical mechanism of orientation tuning are derived. The tuning width is relatively independent of the contrast and angular anisotropy of the visual stimulus. The transient population response to changing of the stimulus orientation exhibits a slow "virtual rotation." Neuronal cross-correlations exhibit long time tails, the sign of which depends on the preferred orientations of the cells and the stimulus orientation.