Kirk N. Gelatt - Essentials of Veterinary Ophthalmology

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A user-friendly reference to basic, foundational information on veterinary ophthalmology This book provides readers with a user-friendly manual to the basics of veterinary ophthalmology. It puts a focus on the most relevant information for clinical practice. Emphasizing canine ophthalmology, the book also covers the foundations of feline, equine, farm animal, and exotic animal ophthalmology. To aid in reader comprehension and information assimilation, a companion website presents review questions and the figures from the book in PowerPoint. Sample topics covered within the work include:
Ophthalmic foundations: ophthalmic development and structure, physiology of the eye and vision, and ocular pharmacology and therapeutics Canine ophthalmology: canine orbit (disease and surgery), canine eyelids (disease and surgery), canine lacrimal apparatus (tear secretion and drainage), canine cornea (diseases and surgery) and canine glaucoma Other species: feline ophthalmology, equine ophthalmology, and food and fiber animal ophthalmology Ophthalmic and systemic diseases: comparative neuro-ophthalmology and systemic disease and the eye
is a useful guide for veterinary students and practitioners looking to build out their core foundations of knowledge within their specific programs of study and disciplines.

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Some species are monochromats. Rod monochromacy is mainly found in some fish species, whereas marine mammal species and a few terrestrial mammalian species, including the owl monkey, are cone monochromats.

Most mammals, including cats, dogs, horses, cattle, goats, sheep, and swine, are dichromats, just like human protanopes or deuteranopes .Horses, for example, have cone opsins with peak absorbance in the blue and green parts of the spectrum, making their color vision comparable to human protanopes . Dogs (and cats), on the other hand, have cone opsins most sensitive to blue and greenish‐yellow, making their color vision more similar to that of human deuteranopes ( Figure 2.19). When light stimulates the two opsins in a dichromat equally (a monochromatic light of a wavelength that coincides with the intersection of the absorption curves), the retina will not be able to distinguish this wavelength from an achromatic stimulus. This neutral point is reported at about 505 nm in the cat, and 480 nm in the dog and horse. Despite having fewer cones than humans and being dichromats, color vision cues seem to be important during daylight conditions for dogs, and it is likely that other mammalian species also take advantage of their ability to discriminate between different wavelengths to enhance their daily lives, and particularly their sexual and feeding behavior.

Some dichromats, including many rodents, such as the mouse, rat, gerbil, and Siberian hamster, have a specialized short‐wavelength opsin that peaks in the UV range of the spectrum rather than in the blue. Hence, they have extended the spectral range of the electromagnetic radiation that they can perceive. Furthermore, some dichromats that have “regular” S‐ and M/L‐cone pigments, such as the reindeer and dog (and most likely the cat, too), have lenses transmitting UV light, which enables them to see in the UV part of the spectrum using their regular cone pigments.

Many modern‐day reptilian, avian, and fish species still have all four ancestral photopigments, including an additional short‐wavelength opsin with peak absorbance in the UV or violet range (355–450 nm) that humans and most domestic mammals have lost, and have thus tetrachromatic vision .

Birds have developed additional unique mechanisms for color vision. Their double cones are used for fine spatial discrimination (visual acuity), while single cones are used for color vision. Oil droplets found in the cones of birds contribute to color perception by filtering out different wavelengths of incoming light and shifting the wavelength sensitivity of the photoreceptor.

Visual Acuity

Visual acuity is the minimal detection power of the eye, or the minimal angle that can be resolved by the eye. There are a number of ways to express visual acuity, but the best known method is based on the Snellen chart. This is determined by the size of letters that a subject can read at a distance of 20 ft, or 6 m. Obviously, determination of Snellen acuity requires verbal cooperation by the test subject and therefore is not applicable in veterinary medicine. In animals, visual acuity can be determined using behavioral discrimination tests, by electrophysiological recordings to determine the smallest pattern that elicits an ERG or cortical response, or by pursuit (i.e., optokinetic) eye responses to determine the smallest stimulus that elicits a tracking eye movement. Acuity is also often determined by theoretical calculations based on cone or RGC density ( Table 2.16).

Figure 219 A colorful dog as seen by a normal trichromat a In b the - фото 81

Figure 2.19 A colorful dog, as seen by a normal trichromat (a). In (b), the color information from the photograph has been extracted. The photograph has been filtered to mimic how a protanope (c), a deuteranope (d), a tritanope (e), and a cone monochromat (f) would perceive the same scene. The protanope and deuteranope can distinguish between short and long wavelengths, whereas the tritanope can subdivide the middle‐to‐long wavelengths into different hues.

Table 2.16 Visual acuity in select species. a

Species Snellen resolution b Spatial frequency (cycles/degree) b Method c References
Eagle ( Aquila audax ) 20/4 140 Behavioral and anatomical Reymond (1985)
Falcon ( Falco berigora ) 20/8 73 Behavioral and anatomical Reymond (1987)
Macaque monkey 20/16 38 Behavioral Merigan & Katz (1990)
Human 20/20 30 Ravikumar et al. (2011)
Horse 20/26 23 Behavioral Timney & Keil (1992)
20/36 16.5 Anatomical Harman et al. (1999)
King penguin Anatomical Coimbra et al. (2012)
Underwater 20/30 20.4
In air 20/40 15.3
Alpaca 20/45 13.4 Anatomical Wang et al. (2015)
Sheep 20/51–20/43 11.7–14 Behavioral Sugnaseelan et al. (2013)
20/86–20/60 7–10 Anatomical Hughes (1977)
Camel 20/60 10 Anatomical Harman et al. (2001)
Dog 20/140–20/52 4.3–11.6 Electrophysiology Odom et al. (1983); Ofri et al. (1993); Murphy et al. (1997)
20/110–20/31 5.5–19.5 Behavioral Lind et al. (2017)
Cat 20/190 3.2 Behavioral Jarvis & Wathes (2007)
20/90 6.5 Electrophysiology Berkley & Watkins (1971)
20/33 18 Anatomical Steinberg et al. (1973); Clark & Clark (2013)
Barn owl Behavioral Orlowski et al. (2012)
20/190 3.2 (Mesopic)
20/500 1.2 (Scotopic)
Rabbit 20/200 3 Electrophysiology Pak (1984)
Cow 20/460–20/230 1.3–2.6 Behavioral Rehkämper et al. (1998, 2000)
Rat Behavioral Prusky et al. (2002)
pigmented 20/600–20/400 1–1.5
albino 20/1200 0.5
Mouse 20/1000 0.58 Behavioral Lehmann et al. (2012)
20/1500 0.39 Optokinetics Lehmann et al. (2012)

aThis table mostly contains data for species commonly seen by veterinary ophthalmologists in clinical and research settings. Avian species have been included to demonstrate their high acuity (eagle, falcon) or the effects of aquatic vision (penguin) and light conditions (owl). The scientific literature reports visual acuity values for numerous other species such as giraffes, elephants, rhinoceros and marsupials that are beyond the scope of this book.

bMost articles report visual acuity in cycles/degree. These values have been converted to Snellen units by the author (R.O.) as most readers are more familiar with this latter scale. Values for Snellen acuity <20/200 have been rounded.

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