Essentials of Veterinary Ophthalmology. Kirk N. Gelatt
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forming layers where they terminate in discrete clusters, generating a retinotopic map of the contralateral visual hemifield (with receptive fields similar in size and response properties to the retinal receptive fields).
Primary Visual Cortex
Brodmann demonstrated that the primary visual cortex (i.e., area 17) receiving the input from the LGN is located in the posterior part of the occipital lobe in a number of species. This area is now usually called V1 (visual area 1) or the striate cortex, after the striae of Gennari. In contrast, all other visual areas in the cortex lacking the stria (which is a myelinated stripe where the LGN axons enter the gray matter of the V1) are termed extrastriate.
V1 has been mapped in several species. In the cat, it occupies the posteromedial portion of the cortex, extending from the crown of the lateral gyrus on the dorsal surface to the superior bank of the splenial sulcus on the medial surface. In the dog, it is located at the junction of the marginal and endomarginal gyri. The striate cortex has also been identified in the horse.
Section III: Vision
Ability to detect light is, of course, fundamental for vision, but other aspects, such as detection of motion and determining other qualities of an object, such as shape and details, color, size, and distance, help to form our visual percept. The processing of the output from the photoreceptors starts in the retina (Figure 2.15), but countless neurons in the brain finally shape and interpret the image of the world around us. Animal visual perception is a subject of great fascination to researchers, clinicians and animal owners. Unfortunately, we can neither tell exactly what an animal sees because they usually cannot tell, nor do we know precisely what there is to see because of the limitations of our own visual system.
Scotopic and Photopic Vision
Photoreceptors can respond to changes in levels of background luminance by processes of adaptation and this results in an extended operating range, allowing the eye optimal performance at a given illumination level. A decrease in background illumination to below 0.03 cd/m2 will deactivate the cone system, resulting in increased light sensitivity (i.e., lower threshold) and scotopic rod vision. An increase in background illumination, to 0.03–3 cd/m2, will lead to mesopic vision in which both the rod and cone systems are active, for example, before dawn or after sunset. Further increase in background illumination above 3 cd/m2, to photopic levels, will result in rod saturation. In such an environment, cones will continue to function, albeit with a higher threshold, or with lower sensitivity.
Figure 2.15 A considerable amount of processing of data from the photoreceptors is performed already in the neuroretina. Left‐hand panels briefly describe the purpose of the computations performed, and the right‐hand column illustrates important elements of the underlying circuits schematically (triangle – neuron; A – amacrine cell; B – bipolar cell; G – RGC; P – photoreceptor; rectangle – temporal filter function; oval – instantaneous rectifier; closed/open circle – sign‐preserving/sign‐inverting synapse. (a) The rod‐to‐rod pathway detects single photons. The output of each rod (noisy tracings) is sent through a bandpass temporal filter followed by a thresholding operation. Signals from several rods are then pooled to and summed by one rod bipolar cell, which shows distinct activations (tracings without noise). (b) The Y‐RGC is activated by texture motion in either direction over its receptive field (red circle). Each movement elicits either transient ON or OFF responses in the bipolar cells, but only the depolarized bipolar cells signal to the ganglion cell that fires transiently to each shift in the grating. (c) An RGC sensitive to local motion fires when the object in its central receptive field moves in different direction that from the background, thus detecting differential motion. This RGC is silent when the object in the center moves in the same direction as the background because the excitatory input in the center is counteracted by inhibitory input from the surround via the amacrine cell. (d) A RGC responds strongly (several spikes) to an approaching dark object, but only weakly to lateral motion. More OFF bipolar cells are excited when a larger part of the receptive field is dark. When the object only moves laterally, the RGC receives both excitatory signals from the OFF bipolar cells and inhibitory signals from amacrine cells activated by ON bipolar cells. (e) Specific RGCs use differences in spike latencies to rapidly encode the structure of an image. RGCs with receptive fields (circles) in the dark part of the image have short latencies, and those in the light part have long latencies. RGCs with receptive fields containing both dark and light areas fire in between, thus indicating the position of the border. Here, signals from both ON and OFF bipolar cells are individually rectified, and the timing difference follows from a delay (Δt) in the ON pathway. (f) Wide‐field amacrine cells (A1) are activated during rapid shifts of the image in the retinal periphery, which suppresses the OFF bipolar cell signal and disinhibits the ON bipolar cell through a local amacrine cell (A2). Hence, this circuit acts like a switch, in this case enabling a signal in the more central part of the retina.
Scotopic Vision
Rods and Rod Pathways
Cones are inactive in scotopic conditions, and in such an environment our fovea becomes a relative blind spot. Instead, scotopic vision is possible because of the molecular and anatomical characteristics of both rods and the rod pathway. The unique features make an individual rod more sensitive than an individual cone. Another important feature that enables sensitive scotopic vision is the converging nature of the rod pathways. In cats, it has been estimated that in the peripheral retina, the output of approximately 75 000 rod photoreceptors converges on about 5000 rod bipolar cells, which output to 250 amacrine cells, that converge on one ganglion cell.
In many animal species, increased number and density of rods enhance scotopic vision. It can be appreciated that dogs have a higher maximal rod concentration than cats, even though most people associate the latter with greater scotopic sensitivity. This discrepancy may be explained by the structure of the tapetum, which is less reflective in dogs than in cats.
Tapetum
One of the most fascinating adaptations for enhanced scotopic vision is the evolution of a reflective tapetum in the choroid. Light photons striking this layer bounce back onto the retina, thus giving them a second chance to be absorbed by the photoreceptors. This second opportunity is not significant in daytime, as cones absorb enough photons during their “first pass” through the retina. In fact, the tapetum has a detrimental effect on visual acuity in broad daylight, as the light is reflected onto a photoreceptor different from the one in the original trajectory. However, at night this detrimental effect on visual resolution is insignificant as cones are inactive. Instead, the retina benefits from the increased probability that rods will absorb the few photons entering the eye in a dim environment, thus enhancing scotopic vision.
Globe Size
The dimensions of the ocular tissues also contribute to improved scotopic sensitivity in many species. For example, the mean diameter of the cornea in cats and humans is 16.5 and 11.7 mm, respectively. Consequently, much more light enters the cat's eye. Next, light must pass through the pupil. The diameter of a mydriatic pupil in cats and humans is about 12 and 8 mm, respectively, translating into a pupillary aperture of 113 and 50 mm2, respectively. As a result, far more light passes through the cornea and pupil to reach the feline retina at night, when the pupil is fully dilated. Indeed, it has been calculated that a fully dilated pupil increases the amount of light reaching the retina by