Abstract
<jats:p>Divisive normalization describes how neuronal responses are scaled by the activity of a broader pool of inputs and accounts for several nonlinear response properties in primary visual cortex (V1). It accurately describes contrast gain control, as well as the response to overlapping gratings. Nevertheless, how this computation is performed by the brain is unclear. One mechanism suggested to underlie divisive normalization in V1 is short-term depression (STD) at thalamocortical synapses. Here, we used a Vglut2-Cre dependent heterozygous deletion of Stxbp1 in mice as an in vivo model for increased STD. This enabled us to test whether STD is responsible for divisive normalization in V1. As expected, responses were shorter in the mutant mice compared to wild-type siblings. Although we did find other differences in visual responses, notably in direction selectivity and response linearity, neither the contrast response function, nor the amount of cross orientation suppression differed between the two groups. We conclude that STD is likely not involved in divisive normalization of visual responses in mouse V1. Instead, short-term plasticity shapes the temporal integration through which selective cortical responses are constructed.</jats:p>