The intensity see more changed every 30 ms and was drawn from a Gaussian distribution

with a constant mean to avoid contributions from luminance adaptation. Temporal contrast also varied randomly by changing the standard deviation of the distribution every 20 s, with each sequence lasting 300 s and having 15 contrasts (Figure 1A). To isolate the strong component of adaptation that occurs prior to spiking (Baccus and Meister, 2002, Kim and Rieke, 2001 and Zaghloul et al., 2005), we digitally removed spikes from the recording to analyze the subthreshold membrane potential. Adaptive properties of neurons have been quantified using a linear-nonlinear (LN) model (see Experimental Procedures) consisting of a linear temporal filter passed through a static nonlinearity. The linear filter represents the average feature that depolarizes the cell, and the nonlinearity represents the average instantaneous comparison between the filtered visual stimulus and the response. Both quantities are average measures given a particular set of stimulus statistics; the underlying system is more complex with additional nonlinearities (Baccus and Meister, 2002 and Kim and Rieke, 2001). Thus, the LN model can reveal and quantify adaptation but does selleck kinase inhibitor not produce adaptation itself. When LN models are used to represent different

time intervals relative to a contrast step, the most accurate linear filter changes, as does the nonlinearity, indicating the presence of an adaptive response (Figure 1B). A high contrast step quickly accelerates temporal processing, as measured by the time to peak of the linear filter, makes the temporal response more differentiating, and decreases the sensitivity, which is defined as the average slope of the nonlinearity (Demb, 2008). High contrast also quickly produces a depolarizing offset, as measured by the average value of the nonlinearity, that then slowly decays. We then tested a new model to capture both the intracellular membrane

potential (Figure 1A) and adaptive properties (Figure 1B) Mannose-binding protein-associated serine protease across multiple contrasts. Many biophysical mechanisms produce changes in gain, including ion channel inactivation, biochemical cascades, receptor desensitization, and synaptic depression (Burrone and Lagnado, 2000, DeVries and Schwartz, 1999 and He et al., 2002). A widely used approach to describe these mechanisms uses a first-order kinetic model, whereby a system transitions between different states and is governed by a set of rate constants (Colquhoun and Hawkes, 1977 and Hodgkin and Huxley, 1952). Initially, we sought to capture adaptive properties with a kinetic model, without regard to any one corresponding mechanism. A simple example of such a model has four states (Figure 2A).