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EyeThe eye is a complex biological device. The functioning of a camera is often compared with the workings of the eye, mostly since both focus light from external objects on a light-sensitive medium. In the case of the camera, this medium is film or an electronic sensor; in the case of the eye, it is an array of visual receptors. However, other than this simple mechanical similarity, the eye has little in common with any type of CCD camera. Light entering the eye is refracted as it passes through the cornea. It then passes through the pupil (controlled by the iris) and is further refracted by the lens. The lens inverts the light and projects an image onto the retina. Image:Cajal Retina.jpg S. Ramón y Cajal, Structure of the Mammalian Retina, 1900 RetinaThe retina consists of a large number of photoreceptor cells which contain a particular protein molecule called an opsin. In humans, there are two types of opsins, rod opsins and cone opsins. Either opsin absorbs a photon (a particle of light) and transmits a signal to the cell through a signal transduction pathway, resulting in hyperpolarization of the photoreceptor. (For more information, see photoreceptor).
In the retina, the photoreceptors synapse directly onto bipolar cells, which in turn synapse onto ganglion cells of the outermost layer, who will then conduct action potentials to the brain. A significant amount of visual processing arises from the patterns of communication between neurons in the retina. About 130 million photoreceptors absorb light, yet roughly 1.2 million axons of ganglion cells transmit information from the retina to the brain. The processing in the retina includes the formation of center-surround receptive fields of bipolar and ganglion cells in the retina, as well as convergence and divergence from photoreceptor to bipolar cell. In addition, other neurons in the retina, particularly horizontal and amacrine cells, transmit information laterally (from a neuron in one layer to an adjacent neuron in the same layer), resulting in more complex receptive fields that can be either indifferent to color and sensitive to motion or sensitive to color and indifferent to motion. The final result of all this processing is five different populations of ganglion cells that send information to the brain: M cells, with large center-surround receptive fields that are sensitive to depth, indifferent to color, and rapidly adapt to a stimulus; P cells, with smaller center-surround receptive fields that are sensitive to color and shape; K cells, with very large center-only receptive fields that are sensitive to color and indifferent to shape or depth; another population that is intrinsically photosensitive; and a final population that is used for eye movements. A recent University of Pennsylvania study calculated the approximate bandwidth of human retinas as 8.75 megabits per second, whereas guinea pig retinas transfer at 875 kilobits. [1] PhotochemistryIn the vision system, retinal, technically called retinene1 or "retinaldehyde", is a light-sensitive retinene molecule found in the photoreceptor cells of the retina. Retinal is the fundamental structure involved in the transduction of light into visual signals, i.e. nerve impulses in the ocular system of the central nervous system. In the presence of light, the retinal molecule changes configuration and as a result a nerve impulse is generated. Fibers to thalamusOptic nerveImage:1543,Vesalius'Fabrica,VisualSystem,V1.jpg Information flow from the eyes (top), crossing at the optic chiasma, joining left and right eye information in the optic tract, and layering left and right visual stimuli in the lateral geniculate nucleus. V1 in red at bottom of image. (1543 image from Andreas Vesalius' Fabrica) The information about the image via the eye is transmitted to the brain along the optic nerve. Different populations of ganglion cells in the retina send information to the brain through the optic nerve. About 90% of the axons in the optic nerve go to the lateral geniculate nucleus in the thalamus. These axons originate from the M, P, and K ganglion cells in the retina. This parallel processing is important for reconstructing the visual world; each type of information will go through a different route to perception. Another population sends information to both the superior colliculus in the medula, which assists in controlling eye movements (saccades).[2] A final population of photosensitive ganglion cells (containing melanopsin) sends information to the pretectum (pupillary reflex), and to several structures involved in the control of circadian rhythms and sleep such as the suprachiasmatic nucleus (SCN, the biological clock), the ventrolateral preoptic nucleus (VLPO, a region involved in sleep regulation).[3] Optic chiasmThe optic nerves from both eyes meet and cross at the optic chiasm, at the base of the hypothalamus of the brain. At this point the information coming both eyes is combined and then splits according to the visual field. The corresponding halves of the field of view (right and left) are sent to the left and right halves of the brain, respectively, to be processed. That is, the right side of primary visual cortex deals with the left half of the field of view from both eyes, and similarly for the left brain.[2] A small region in the center of the field of view is processed redundantly by both halves of the brain. Optic tractInformation from the right visual field (now on the left side of the brain) travels in the left optic tract. Information from the left visual field travels in the right optic tract. Each optic tract terminates in the lateral geniculate nucleus (LGN) in the thalamus. Image:Lateral geniculate nucleus.png Six layers in the LGN Lateral geniculate nucleusThe lateral geniculate nucleus (LGN) is a sensory relay nucleus in the thalamus of the brain. The LGN consists of six layers in humans and other primates starting from catarhinians, including cercopithecidae and apes. Layers 1, 4, and 6 correspond to information from one eye; layers 2, 3, and 5 correspond to information from the other eye. Layer one (1) contains M cells, which correspond to the M (magnocellular) cells of the optic nerve of the opposite eye, and are concerned with depth or motion. Layers four and six (4 & 6) of the LGN also connect to the opposite eye, but to the P cells (color and edges) of the optic nerve. By contrast, layers two, three and five (2, 3, & 5) of the LGN connect to the M cells and P (parvocellular) cells of the optic nerve for the same side of the brain as its respective LGN. The six layers of the LGN are the area of a credit card, but about three times the thickness of a credit card, rolled up into two ellipsoids about the size and shape of two small birds eggs. In between the six layers are smaller cells that receive information from the K cells (color) in the retina. The neurons of the LGN then relay the visual image to the primary visual cortex (V1) which is located at the back of the brain (caudal end) in the occipital lobe in and close to the calcarine sulcus. Image:Gray722.png Gray's FIG. 722– Scheme showing central connections of the optic nerves and optic tracts. Optic radiationThe optic radiations carries information from the thalamic lateral geniculate nucleus to layer 4 of the visual cortex. The P layer neurons of the LGN relay to V1 layer 4C β. The M layer neurons relay to V1 layer 4C α. The K layer neurons in the LGN relay to large neurons called blobs in layers 2 and 3 of V1. There is a direct correspondence from an angular position in the field of view of the eye, all the way through the optic tract to a nerve position in V1. At this juncture in V1, the image path ceases to be straightforward; there is more cross-connection within the visual cortex. Visual cortexImage:Ba 17 18 19.png Visual cortex: V1, V2, V3, V4, V5 (also called MT) The visual cortex is the most massive system in the human brain and is responsible for higher-level processing of the visual image. It lies at the rear of the brain (highlighted in the image), above the cerebellum. The interconnections between layers of the cortex, the thalamus, the cerebellum, the hippocampus and the remainder of the areas of the brain are under active investigation. Currently, much of what is known stems from patients with damage to known areas of the brain, with a corresponding study of the cognitive functions which have been spared. See visual modularity for a discussion of the modular thesis of visual perception. See alsoReferences
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