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Eye, Retina - Degeneration

Image of retina degeneration in the eye from a male F344/N rat in a chronic study
Eye, Retina - Normal in a male F344/N rat from a chronic study. Normal retina for comparison to Figures 2 and 3.
Figure 1 of 3
Image of retina degeneration in the eye from a male F344/N rat in a chronic study
Eye, Retina - Degeneration in a male F344/N rat from a chronic study. Mild retinal degeneration, featuring loss of rod and cone photoreceptor processes, single-cell necrosis of outer nuclear layer photoreceptor cells, hypocellularity and disorganization of the inner and outer nuclear layers, and narrowing or absence of the plexiform layers.
Figure 2 of 3
Image of retina degeneration in the eye from a male F344/N rat in a chronic study
Eye, Retina - Degeneration in a male F344/N rat from a chronic study. Marked retinal degeneration, featuring overall thinning, architectural disruption, loss of almost all cellular elements, and complete absence of the rod and cone photoreceptors and the plexiform layers.
Figure 3 of 3
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comment:

Retinal degeneration in rats and mice can occur as an aging change or secondary to various insults, such as physical trauma, retinal detachment, inflammation, infectious agents (e.g., viruses), vascular derangements (e.g., infarction), increased intraocular pressure, and nutritional deficiencies. Numerous heritable retinal degenerations have also been documented in various strains of laboratory mice and rats. So-called light-induced retinal degeneration can occur when rats and mice (especially albino strains) are exposed to overly intense ambient light. Retinal degeneration can also be a direct toxic effect of systemically or topically administered chemical agents. Spontaneously occurring retinal degeneration of uncertain etiology has also been reported in laboratory rats and mice. In many types of retinal degeneration, the most commonly affected retinal neurons are the rod and cone photoreceptors and/or the ganglion cells. Depending on the cause, degenerative changes may be localized (or more extensive) in particular retinal topographic regions (i.e., superior vs. inferior, central vs. peripheral).

Mild retinal degeneration ( Figure 2image opens in a pop-up window , compare to Figure 1image opens in a pop-up window ) typically consists of loss of the rod and cone photoreceptor processes, apoptosis of outer nuclear layer photoreceptor cells, hypocellularity and disorganization of the inner and outer nuclear layers, and narrowing or absence of the plexiform layers. More pronounced retinal degeneration ( Figure 3image opens in a pop-up window , compare to Figure 1image opens in a pop-up window ) is typically characterized by overall thinning, architectural disruption, and loss of cellular elements, as well as complete absence of the rod and cone photoreceptors and the plexiform layers. Degenerate retinas may also exhibit other morphologic features, such as diffuse or nodular proliferation of retinal glial cells (e.g., Müller cells and astrocytes), fixed fold and rosette-like formations, and intraretinal cavitations or cysts ("microcystoid" formation and retinoschisis), as well as concurrent proliferation and/or intraretinal migration of the adjacent retinal pigment epithelium.

Rats and mice can also exhibit an incidental aging change known as peripheral retinal degeneration ( and , compare to ), which is characterized by marked thinning of the peripheral retina due to hypocellularity or absence of retinal layers. Although not illustrated, cystic cavitations ("microcystoid" change) are also common features of this peripheral age-related degeneration.

recommendation:

Retinal degeneration should be diagnosed and graded whenever present. The location (peripheral or central) and extent of the lesion within the retina, as well as the retinal layers affected, should be described in the pathology narrative. The pathologist's opinion as to whether it is the peripheral, age related, background form of the lesion (or an exacerbation thereof) or a primary treatment-related lesion should be included in the pathology narrative. The various morphologic features of retinal degeneration (hypocellularity of specific layers, rod and cone photoreceptor process loss, etc.) should not be diagnosed separately but should be described in the narrative. The presence of retinal degeneration should prompt careful examination of the optic nerve for concurrent lesions.

references:

Breider MA, Pilcher GD, Graziano MJ, Gough AW. 1998. Retinal degeneration in rats induced by CI-1010, a 2-nitroimidazole radiosensitizer. Toxicol Pathol 26:234-239.
Full Text: http://tpx.sagepub.com/content/26/2/234.full.pdf+html

Del Cerro M, Grover D, Monjan A, Pfau C, Dematte J. 1984. Congenital retinitis in the rat following maternal exposure to lymphocytic choriomeningitis virus. Exp Eye Res 38:313-324.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/6723808

De Vera Mudry MC, Kronenberg S, Komatsu S-I, Aguirre GD. 2013. Blinded by the light: Retinal phototoxicity in the context of safety studies. Toxicol Pathol 41: 813-825.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/23271306

DiLoreto DA Jr, Del Cerro C, Cox C, Del Cerro M. 1998. Changes in visually guided behavior of Royal College of Surgeons rats as a function of age: A histologic, morphometric, and functional study. Invest Ophthalmol Vis Sci 39:1058-1063.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/9579488

Frame SR, Carlton WW. 1991. Toxic retinopathy, rat, mouse, and hamster. In: International Life Sciences Institute Monographs on Pathology of Laboratory Animals, Vol 10, Eye and Ear (Jones TC, Mohr U, Hunt RD, eds). Springer, Berlin, 116-124.

Frame SR, Slone TW. 1966. Nonneoplastic and neoplastic changes in the eye. In: Pathobiology of the Aging Mouse, Vol 2 (Mohr U, Dungworth DL, Capen CC, Carlton WW, Sundberg JP, Ward JM, eds). ILSI Press, Washington, DC, 97-103.

Geiss V, Yoshitomi K. 1991. Eyes. In: Pathology of the Mouse: Reference and Atlas (Maronpot RR, Boorman GA, Gaul BW, eds). Cache River Press, Vienna, IL, 471-489.
Abstract: http://www.cacheriverpress.com/books/pathmouse.htm

Greaves P. 2007. Nervous system and special sense organs. In: Histopathology of Preclinical Toxicity Studies: Interpretation and Relevance in Drug Safety Evaluation, 3rd ed. Academic Press, San Diego, CA, 861-933.
Abstract: http://www.sciencedirect.com/science/book/9780444527714

Illanes O, Anderson S, Niesman M, Zwick L, Jessen BA. 2006. Retinal and peripheral nerve toxicity induced by the administration of a pan-cyclin dependent kinase (cdk) inhibitor in mice. Toxicol Pathol 34:243-248.
Full Text: http://tpx.sagepub.com/content/34/3/243.full

Lai Y-L, Jacoby RL, Jonas AM. 1978. Age-related and light-associated retinal changes in Fischer rats. Invest Ophthalmol Vis Sci 17:634-638.
Abstract: https://pubmed.ncbi.nlm.nih.gov/669893/

Lee EW, Render JA, Garner CD, Brady AN, Li LC. 1990. Unilateral degeneration of retina and optic nerve in Fischer-344 rats. Vet Pathol 27:439-444.
Abstract: http://vet.sagepub.com/content/27/6/439.short

Mecklenburg L, Schraermeyer U. 2007. An overview on the toxic morphological changes in the retinal pigment epithelium after systemic compound administration. Toxicol Pathol 35:252-267.
Full Text: http://tpx.sagepub.com/content/35/2/252.full

Montalbán-Soler L, Alarcón-Martínez L, Jiménez-López M, Salias-Navarro M, Galindo-Romero C, Bezerrade Sá F, García-Ayoso D, Avilés-Trigueros M, Vidal-Sanz M, Agudo-Barrioso M, Villegas-Pérez M. 2012. Retinal compensatory changes after the light damage in albino mice. Mol Vis 18:675-693.
Full Text: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325904/

National Toxicology Program. 2012. NTP TR-572. Toxicology and Carcinogenesis Studies of Methyl trans-Styryl Ketone (CAS No. 1896-62-4) in F344/N Rats and B6C3F1 Mice (Feed and Dermal Studies). NTP, Research Triangle Park, NC.
Abstract: https://ntp.niehs.nih.gov/go/36154

Nyska A, Maronpot RR, Ghanayem BI. 1999. Ocular thrombosis and retinal degeneration induced in female F344 rats by 2-butoxyethanol. Hum Exp Toxicol 18:577-582.
Abstract: http://het.sagepub.com/content/18/9/577.abstract

Ramos M, Reilly CM, Bolon B. 2011. Toxicological pathology of the retina and optic nerve. In: Fundamental Neuropathology for Pathologists and Toxicologists (Bolon B, Butt MT, eds). Wiley, Hoboken, NJ, 385-412.
Abstract: http://onlinelibrary.wiley.com/doi/10.1002/9780470939956.ch24/summary

Rao GN. 1991. Light intensity-associated eye lesions of Fischer 344 rats in long-term studies. Toxicol Pathol 19:148-155.
Abstract: http://tpx.sagepub.com/content/19/2/148.short

Seoane A, Espejo M, Pallàs M, Rodriguez-Farre E, Ambrosio S, Llorens J. 1999. Degeneration and gliosis in rat retina and central nervous system following 3,3'-iminodipropionitrile exposure. Brain Res 833:258-271.
Full Text: http://toxsci.oxfordjournals.org/content/88/2/456.full.pdf

Serfilippi LM, Stackhouse Pallman DR, Gruebbel MM, Kern TJ, Spainhour CB. 2004. Assessment of retinal degeneration in outbred albino mice. Comp Med 54:69-76.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/15027621

Smith RS, Hawes NL, Chang B, Nishina PM. 2002. Retina. In: Systematic Evaluation of the Mouse Eye: Anatomy, Pathology, and Biomethods (Smith RS, John SWM, Nishina PM, Sundberg JP, eds). CRC Press, Boca Raton, FL, 195-225.

Sun H, Wang Y, Pang I-H, Shen J, Tang X, Li Y, Liu C, Li B. 2011. Protective effect of a JNK inhibitor against retinal ganglion cell loss induced by acute moderate ocular hypertension. Mol Vis 17:864-875.
Full Text: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081797/

Tanito M, Kaidzu S, Ohira A, Anderson RE. 2008. Topography of retinal damage in light-exposed albino rats. Exp Eye Res 87:292-295.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/18586030

Taradach C, Greaves P, Rubin LF. 1984. Spontaneous eye lesions in laboratory animals: Incidence in relation to age. Crit Rev Toxicol 12:121-147.
Abstract: https://www.ncbi.nlm.nih.gov/pubmed/6368130

Wasowicz M, Morice C, Ferrari P, Callebert J, Versaux-Botteri C. 2002. Long-term effects of light damage on the retina of albino and pigmented rats. Invest Ophthalmol Vis Sci 43:813-820.
Abstract: https://pubmed.ncbi.nlm.nih.gov/11867603/

Weisse I. 1995. Changes in the aging rat retina. Ophthalmic Res 27(Suppl 1):154-163.
Abstract: http://www.karger.com/Article/Abstract/267862

Weisse I. 1996. Aging and ocular changes. In: Pathobiology of the Aging Mouse, Vol 2 (Mohr U, Dungworth DL, Capen CC, Carlton WW, Sundberg JP, Ward JM, eds). ILSI Press, Washington, DC, 65-86.

Yoshitomi K, Boorman GA. 1990. Eye and associated glands. In: Pathology of the Fischer Rat: Reference and Atlas (Boorman GA, Eustis SL, Elwell MR, Montgomery CA, MacKenzie WF, eds). Academic Press, San Diego, CA, 239-260.
Abstract: https://www.ncbi.nlm.nih.gov/nlmcatalog/9002563

Yoshizawa K, Kuro-Kuwata M, Sasaki T, Lai C Y-C, Kanematsu S, Miki H, Kimura-Kawanaka A, Uehara N, Yuri T, Tsubara A. 2011. Retinal degeneration induced in adult mice by a single intraperitoneal injection of N-ethyl-N-nitrosurea. Toxicol Pathol 39:606-613.
Full Text: http://tpx.sagepub.com/content/39/4/606.full