Browse > Article
http://dx.doi.org/10.4142/jvs.2021.22.e65

Assessment of the pigeon (Columba livia) retina with spectral domain optical coherence tomography  

Kim, Sunhyo (Department of Veterinary Clinical Sciences, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University)
Kang, Seonmi (Department of Veterinary Clinical Sciences, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University)
Susanti, Lina (Department of Veterinary Clinical Sciences, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University)
Seo, Kangmoon (Department of Veterinary Clinical Sciences, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University)
Publication Information
Journal of Veterinary Science / v.22, no.5, 2021 , pp. 65.1-65.12 More about this Journal
Abstract
Background: To assess the normal retina of the pigeon eye using spectral domain optical coherence tomography (SD-OCT) and establish a normative reference. Methods: Twelve eyes of six ophthalmologically normal pigeons (Columba livia) were included. SD-OCT images were taken with dilated pupils under sedation. Four meridians, including the fovea, optic disc, red field, and yellow field, were obtained in each eye. The layers, including full thickness (FT), ganglion cell complex (GCC), thickness from the retinal pigmented epithelium to the outer nuclear layer (RPE-ONL), and from the retinal pigmented epithelium to the inner nuclear layer (RPE-INL), were manually measured. Results: The average FT values were significantly different among the four meridians (p < 0.05), with the optic disc meridian being the thickest (294.0 ± 13.9 ㎛). The average GCC was thickest in the optic disc (105.3 ± 27.1 ㎛) and thinnest in the fovea meridian (42.8 ± 15.3 ㎛). The average RPE-INL of the fovea meridian (165.5 ± 18.3 ㎛) was significantly thicker than that of the other meridians (p < 0.05). The average RPE-ONL of the fovea, optic disc, yellow field, and red field were 91.2 ± 5.2 ㎛, 87.7 ± 5.3 ㎛, 87.6 ± 6.5 ㎛, and 91.4 ± 3.9 ㎛, respectively. RPE-INL and RPE-ONL thickness of the red field meridian did not change significantly with measurement location (p > 0.05). Conclusions: Measured data could be used as normative references for diagnosing pigeon retinopathies and further research on avian fundus structure.
Keywords
Fovea; optical coherence tomography; pecten; pigeon; retina;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Rauscher FG, Azmanis P, Korber N, Koch C, Hubel J, Vetterlein W, et al. Optical coherence tomography as a diagnostic tool for retinal pathologies in avian ophthalmology. Invest Ophthalmol Vis Sci. 2013;54(13):8259-8269.   DOI
2 Ofri R, Ekesten B. Baseline retinal OCT measurements in normal female beagles: the effects of eccentricity, meridian, and age on retinal layer thickness. Vet Ophthalmol. 2020;23(1):52-60.   DOI
3 Famose F. Assessment of the use of spectral domain optical coherence tomography (SD-OCT) for evaluation of the healthy and pathological cornea in dogs and cats. Vet Ophthalmol. 2014;17(1):12-22.   DOI
4 Espinheira Gomes F, Abou-Madi N, Ledbetter EC, McArt J. Spectral-domain optical coherence tomography imaging of normal foveae: A pilot study in 17 diurnal birds of prey. Vet Ophthalmol. 2020;23(2):347-357.   DOI
5 McLellan GJ, Rasmussen CA. Optical coherence tomography for the evaluation of retinal and optic nerve morphology in animal subjects: practical considerations. Vet Ophthalmol. 2012;15 Suppl 2:13-28.   DOI
6 Mariani AP. Neuronal and synaptic organization of the outer plexiform layer of the pigeon retina. Am J Anat. 1987;179(1):25-39.   DOI
7 Huang Y, Cideciyan AV, Papastergiou GI, Banin E, Semple-Rowland SL, Milam AH, et al. Relation of optical coherence tomography to microanatomy in normal and rd chickens. Invest Ophthalmol Vis Sci. 1998;39(12):2405-2416.
8 Moayed AA, Hariri S, Song ES, Choh V, Bizheva K. In vivo volumetric imaging of chicken retina with ultrahigh-resolution spectral domain optical coherence tomography. Biomed Opt Express. 2011;2(5):1268-1274.   DOI
9 Rosolen SG, Riviere ML, Lavillegrand S, Gautier B, Picaud S, LeGargasson JF. Use of a combined slit-lamp SD-OCT to obtain anterior and posterior segment images in selected animal species. Vet Ophthalmol. 2012;15 Suppl 2:105-115.   DOI
10 Karimi V, Asadi F, Rajaei SM, Golabdar S. Intraocular pressure measurements using rebound tonometry in eight different species of companion birds. J Avian Med Surg. 2020;34(4):338-342.
11 Pumphrey RJ. The theory of the fovea. J Exp Biol. 1948;25(3):299-312.   DOI
12 Baine K, Hendrix DV, Kuhn SE, Souza MJ, Jones MP. The efficacy and safety of topical rocuronium bromide to induce bilateral mydriasis in hispaniolan amazon parrots (Amazona ventralis). J Avian Med Surg. 2016;30(1):8-13.   DOI
13 Petritz OA, Guzman DS, Gustavsen K, Wiggans KT, Kass PH, Houck E, et al. Evaluation of the mydriatic effects of topical administration of rocuronium bromide in Hispaniolan Amazon parrots (Amazona ventralis). J Am Vet Med Assoc. 2016;248(1):67-71.   DOI
14 Lim J, Kang S, Park S, Park E, Nam T, Jeong S, et al. Intraocular pressure measurement by rebound tonometry (tonovet) in normal pigeons (Columba livia). J Avian Med Surg. 2019;33(1):46-52.   DOI
15 Hodos W, Bessette BB, Macko KA, Weiss SR. Normative data for pigeon vision. Vision Res. 1985;25(10):1525-1527.   DOI
16 Hodos W, Miller RF, Fite KV. Age-dependent changes in visual acuity and retinal morphology in pigeons. Vision Res. 1991;31(4):669-677.   DOI
17 Fitzgerald ME, Tolley E, Frase S, Zagvazdin Y, Miller RF, Hodos W, et al. Functional and morphological assessment of age-related changes in the choroid and outer retina in pigeons. Vis Neurosci. 2001;18(2):299-317.   DOI
18 Querubin A, Lee HR, Provis JM, O'Brien KM. Photoreceptor and ganglion cell topographies correlate with information convergence and high acuity regions in the adult pigeon (Columba livia) retina. J Comp Neurol. 2009;517(5):711-722.   DOI
19 Gelatt KN, Gilger BC, Kern TJ. Chapter 2. Ophthalmic anatomy. In: Samuelson DA, editor. Veterinary Ophthalmology, 5th ed. Ames: Wiley-Blackwell; 2013, 39-668.
20 Azmanis P, Rauscher FG, Werner B. The additional diagnostic value of optical coherence tomography (OCT) and its application procedure in a wide variety of avian Species. J Clin Exp Ophthalmol. 2015;6(03):431.
21 Ruggeri M, Major JC Jr, McKeown C, Knighton RW, Puliafito CA, Jiao S. Retinal structure of birds of prey revealed by ultra-high resolution spectral-domain optical coherence tomography. Invest Ophthalmol Vis Sci. 2010;51(11):5789-5795.   DOI
22 Barsotti G, Briganti A, Spratte JR, Ceccherelli R, Breghi G. Mydriatic effect of topically applied rocuronium bromide in tawny owls (Strix aluco): comparison between two protocols. Vet Ophthalmol. 2010;13 Suppl:9-13.   DOI
23 Frenkel S, Morgan JE, Blumenthal EZ. Histological measurement of retinal nerve fibre layer thickness. Eye (Lond). 2005;19(5):491-498.   DOI
24 Bringmann A. Structure and function of the bird fovea. Anat Histol Embryol. 2019;48(3):177-200.   DOI
25 Maggs DJ, Miller PE, Ofri R. Slatter's Fundamentals of Veterinary Ophthalmology. 6th ed. St. Louis: Elsevier Inc.; 2018, 347-398.
26 Jones MP, Pierce KE Jr, Ward D. Avian vision: a review of form and function with special consideration to birds of prey. J Exot Pet Med. 2007;16(2):69-87.   DOI