S. H. DeVries investigated how parallel pathways in the retina extract different temporal components from a shared cone cell signal. In a 2000 study, simultaneous recordings from synaptically connected cone cells and OFF retinal bipolar cells linked distinct bipolar-cell types to different AMPA receptors or kainate receptors.[ref]
The glutamate signal released by one cone cell can therefore enter several postsynaptic channels with different response dynamics. The study combined paired measurements with receptor-selective pharmacology in ground-squirrel retina, making it possible to compare the input and output at an identified connection.[ref]
The motivating question is how the same changing light signal can support both a response to a rapid transition and a response to a more sustained change. Different receptor kinetics supply one experimentally testable part of that explanation. A common transmitter does not require identical temporal filtering in every receiving neuron; neither does a result in these cell types establish a universal receptor assignment across every species and retina.

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