Unlike most sensory receptor cells, photoreceptors actually become
hyperpolarized when stimulated; and conversely are
depolarized when not stimulated. This means that glutamate is released continuously when the cell is unstimulated, and stimulus causes release to stop. In the dark, cells have a relatively high concentration of
cyclic guanosine 3'-5' monophosphate (cGMP), which opens
cGMP-gated ion channels. These channels are nonspecific, allowing movement of both sodium and calcium ions when open. The movement of these positively charged ions into the cell (driven by their respective
electrochemical gradient) depolarizes the membrane, and leads to the release of the neurotransmitter
glutamate.
When light hits a photoreceptive pigment within the photoreceptor cell, the pigment changes shape. The pigment, called iodopsin or rhodopsin, consists of large proteins called opsin (situated in the plasma membrane), attached to a covalently bound prosthetic group: an organic molecule called retinal (a derivative of vitamin A). The retinal exists in the 11-cis-retinal form when in the dark, and stimulation by light causes its structure to change to all-trans-retinal. This structural change causes opsin (a
G protein-coupled receptor) to activate its G protein
transducin, which leads to the activation of
cGMP phosphodiesterase, which breaks cGMP down into 5'-GMP. Reduction in cGMP allows the ion channels to close, preventing the influx of positive ions, hyperpolarizing the cell, and stopping the release of neurotransmitters.
[16] The entire process by which light initiates a sensory response is called
visual phototransduction.