DOI QR코드

DOI QR Code

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)
  • 투고 : 2021.03.23
  • 심사 : 2021.07.08
  • 발행 : 2021.09.30

초록

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.

키워드

과제정보

This study was supported by the BK21 PLUS Program for Creative Veterinary Science Research and the Research Institute for Veterinary Science (RIVS), College of Veterinary Medicine, Seoul National University, Seoul 08826, Korea.

참고문헌

  1. 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. https://doi.org/10.1053/j.jepm.2007.03.012
  2. 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.
  3. 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. https://doi.org/10.1167/iovs.13-11922
  4. 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. https://doi.org/10.1111/vop.12683
  5. 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. https://doi.org/10.1111/vop.12028
  6. 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. https://doi.org/10.1111/vop.12732
  7. 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. https://doi.org/10.1111/j.1463-5224.2012.01045.x
  8. Gelatt KN, Gilger BC, Kern TJ. Chapter 2. Ophthalmic anatomy. In: Samuelson DA, editor. Veterinary Ophthalmology, 5th ed. Ames: Wiley-Blackwell; 2013, 39-668.
  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. https://doi.org/10.1111/j.1463-5224.2012.01037.x
  10. 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. https://doi.org/10.1002/cne.22178
  11. 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.
  12. 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. https://doi.org/10.1364/BOE.2.001268
  13. 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. https://doi.org/10.1167/iovs.10-5633
  14. 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. https://doi.org/10.1647/2015-083
  15. 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. https://doi.org/10.2460/javma.248.1.67
  16. 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. https://doi.org/10.1111/j.1463-5224.2010.00773.x
  17. 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. https://doi.org/10.1647/2017-329
  18. 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.
  19. Frenkel S, Morgan JE, Blumenthal EZ. Histological measurement of retinal nerve fibre layer thickness. Eye (Lond). 2005;19(5):491-498. https://doi.org/10.1038/sj.eye.6701569
  20. Mariani AP. Neuronal and synaptic organization of the outer plexiform layer of the pigeon retina. Am J Anat. 1987;179(1):25-39. https://doi.org/10.1002/aja.1001790105
  21. Pumphrey RJ. The theory of the fovea. J Exp Biol. 1948;25(3):299-312. https://doi.org/10.1242/jeb.25.3.299
  22. Bringmann A. Structure and function of the bird fovea. Anat Histol Embryol. 2019;48(3):177-200. https://doi.org/10.1111/ahe.12432
  23. Hodos W, Bessette BB, Macko KA, Weiss SR. Normative data for pigeon vision. Vision Res. 1985;25(10):1525-1527. https://doi.org/10.1016/0042-6989(85)90231-7
  24. Hodos W, Miller RF, Fite KV. Age-dependent changes in visual acuity and retinal morphology in pigeons. Vision Res. 1991;31(4):669-677. https://doi.org/10.1016/0042-6989(91)90008-S
  25. Maggs DJ, Miller PE, Ofri R. Slatter's Fundamentals of Veterinary Ophthalmology. 6th ed. St. Louis: Elsevier Inc.; 2018, 347-398.
  26. 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. https://doi.org/10.1017/S0952523801182143