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Comparison of the human electro-oculographic response to green and near-ultraviolet stimuli

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Abstract

We recorded the electro-oculogram from 27 normal subjects by means of green and near-ultraviolet (UVA) stimulation. After a 40-minute dark-adaptation period, baseline responses were recorded. In response to the green stimulus, the electro-oculogram increased from this level by an average (± standard error of the mean) of 49.5% ±4.0%. Although the predicted scotopic effectiveness of the ultraviolet stimulus was more than 3 log units below that of the green stimulus, the near-ultraviolet-induced electro-oculogram increased to an average of 21.9% ±3.0% above baseline. This response cannot be due to lens fluorescence to the near-ultraviolet stimulus, since two aphakic subjects had electro-oculographic responses of 32% and 76% above baseline to near-ultraviolet stimuli. Neither the green nor the ultraviolet electro-oculogram changed significantly with age. These large responses to near-ultraviolet stimulation demonstrate the need for standardizing light sources for electro-oculographic testing because the degree of near-ultraviolet irradiance varies considerably according to their design characteristics.

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References

  1. Arden GB, Barrada A, Kelsey JH. New clinical test of retinal function based upon the standing potential of the eye. Br J Ophthalmol 1962; 46: 449–67.

    Google Scholar 

  2. Steinberg RH, Linsenmeier RA, Griff ER. Retinal pigment epithelial cell contributions to the electroretinogram and electrooculogram. In: Osborne N, Chader G, eds. Progress in retinal research. New York: Pergamon Press, 1985; 4: 33–66.

    Google Scholar 

  3. Fishman GA. The electro-oculogram in retinal disorders. In: Fishman GA, Sokol S, eds. Electrophysiological testing in disorders of the retina, optic nerve and visual pathway. San Francisco: American Academy of Ophthalmology, 1990: 91–103.

    Google Scholar 

  4. Jones RM, Stevens TS, Gould S. Normal EOG values of young subjects. Doc Ophthalmol Proc Ser 1977; 13: 93–7.

    Google Scholar 

  5. Arden GB, Kelsey JH. Some observations on the relationship between the standing potential of the human eye and the bleaching and regeneration of visual purple. J Physiol 1962; 161: 205–26.

    Google Scholar 

  6. Elenius V, Lehtonen J. Spectral sensitivity of the standing potential of the human eye. Acta Ophthalmol 1962; 40: 559–66.

    Google Scholar 

  7. Friedman AH. The importance of defining light parameters in chronobiological studies. Chronobiol Int 1984; 1: 229–30.

    Google Scholar 

  8. Taumer R, Hennig J, Pernice D. The ocular dipole. A damped oscillator stimulated by the speed of change in illumination. Vision Res 1974; 14: 637–45.

    Google Scholar 

  9. Reimslag F, Lunel HV, Spekreijse H. lectrooculogram. A refinement of the method, Doc Ophthalmol 1990; 73: 369–75.

    Google Scholar 

  10. Dawson WM, Maida TM. Reduced variability in the electrooculogram. Am J Ophthalmol 1984; 97: 395–6.

    Google Scholar 

  11. Maggiano JM, Marchese AL, Friedman AH. The electrooculogram in response to near UV and near IR [ARVO Abstracts]. 1975: 55.

  12. Wyszecki G, Stiles WS. Color science. Concepts and methods, quantitative data and formulae, 2nd ed. New York: John Wiley & Sons, 1989.

    Google Scholar 

  13. Sliney DH, Freasier BC. Evaluation of optical radiation hazards. Appl Opt 1973; 12: 1–22.

    Google Scholar 

  14. Lerman S. Lens proteins and fluorescence. Isr J Med Sci 1972; 8: 1583–9.

    Google Scholar 

  15. Zigman S, Groff J, Yulo T, Griess G. Light extinction and protein in lens. Exp Eye Res 1976; 23: 555–67.

    Google Scholar 

  16. Geeraets WJ, Berry ER. Ocular spectral characteristics as related to hazards from lasers and other light sources. Am J Ophthalmol 1968; 66: 15–20.

    Google Scholar 

  17. Boettner EA, Wolter JR. Transmission of the ocular media. Invest Ophthalmol 1962; 1: 776–83.

    Google Scholar 

  18. Williams TT, White CW, Stark WS. Ultraviolet visibility after cataract extraction. Invest Ophthalmol Vis Sci 1983; 24 (suppl): 185.

    Google Scholar 

  19. Tan KEWP. Vision in the ultraviolet. Doctoral thesis. Utrecht, 1972.

  20. Wald G, Brown PK, Smith PH. Iodopsin. J Gen Physiol 1954; 38: 623–81.

    Google Scholar 

  21. Sliney DH, Rachlin JA, Marshall WJ. Evaluation of hyperbilirubinemia lamps. Radiation Protection Spectral Study No. 42–025–74/75. Aberdeen Proving Ground, Md: US Army Environmental Health Agency, 1974: 1–13.

    Google Scholar 

  22. International Standardization Committee, International Society for the Clinical Electrophysiology of Vision. Standard for clinical electroretinography. Arch Ophthalmol 1989; 107: 816–9.

    Google Scholar 

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Marchese, A.L., Maggiano, J.M. & Friedman, A.H. Comparison of the human electro-oculographic response to green and near-ultraviolet stimuli. Doc Ophthalmol 79, 117–124 (1992). https://doi.org/10.1007/BF00156571

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