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Empiric limits of rod photocurrent component underlying a-wave response in the electroretinogram

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Abstract

The corneally recorded rod photocurrent component (photoresponse) underlying the a-wave feature of the electroretinogram was analyzed. The results set empiric limits on critical photoresponse variables. Measurements were obtained from four normal adult subjects on a-wave amplitude, a-wave velocity, b-wave amplitude, b-wave implicit time and b-wave height above baseline. At high intensity, interference from the b-wave component was minimized and the amplitude of the saturated photoresponse component was approximated by the a-wave feature. At lower intensities, the a-wave feature represented progressively less of the underlying photoresponse amplitude. Photoresponse amplitude saturation was signaled by the abrupt slowing of the rate of decline of b-wave peak latency and occurred at an intensity about 2.5 log units above the first appearance of the b-wave. At the intensity of photoresponse saturation, the peak amplitude of the a-wave feature was only about 25% of the maximum amplitude of the underlying photoresponse component. A-wave leading edge velocity was found to increase up to 3 log units above the intensity of photoresponse amplitude saturation and to provide a good estimate of photoresponse velocity at higher intensities. A cascaded low-pass filter model with modifications to accommodate amplitude and timing nonlinearities was used to generate a set of probable underlying photoresponses from the analysis of a-wave amplitude and velocity. Movement of the a-wave leading edge to the left at higher intensities in algebraic combination with a static b-wave leading edge above the intensity of photoresponse amplitude saturation was found to explain the second rise of the b-wave amplitude function and the decline of b-wave amplitude above baseline at high intensities. This analysis provides a basis for modeling the underlying photoresponse on a biochemical level and for interpreting photoreceptor damage in disease states.

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References

  1. Johnson MA, Marcus S, Elman MJ, McPhee TJ. Electroretinographic abnormalities associated with neovascularization in central retinal vein occlusion. Arch Ophthalmol 1988; 106: 348–52.

    Google Scholar 

  2. Kaye SB, Harding SP. Early electroretinography in unilateral central retinal vein occlusion as a predictor of rubeosis iridis. Arch Ophthalmol 1988; 106: 353–6.

    Google Scholar 

  3. Breton ME, Quinn GE, Keene SS, et al. Electroretinogram parameters at presentation as predictors of rubeosis in central retinal vein occlusion patients. Ophthalmology 1989; 96: 1343–52.

    Google Scholar 

  4. Bresnich GH, Palta M. Temporal aspects of the electroretinogram in diabetic retinopathy. Arch Ophthalmol 1987; 105: 660–4.

    Google Scholar 

  5. Breton ME, Montzka DP, Brucker AJ, Quinn GE. Electroretinogram interpretation in central retinal vein occlusion. Ophthalmology. 1991; 98: 1837–44.

    Google Scholar 

  6. Granit R. The components of the retinal action potential in mammals and their relation to the discharge in the optic nerve. J Physiol 1933; 77: 207–39.

    Google Scholar 

  7. Arden GB. The retina. Neurophysiology. In: The eye. New York: Academic Press, 1976; chap. 7.

    Google Scholar 

  8. Penn RD, Hagins WA. Signal transmission along retinal rods and the origin of the electroretinographic a-wave. Nature 1969; 223: 201–5.

    Google Scholar 

  9. Stryer L. Molecular basis of visual excitation. Cold Spring Harbor Symposia on Quantitative Biology 1988; 53.

  10. Pugh EN, Lamb TD. Minireview. Cyclic GMP and calcium. The internal messengers of excitation and adaptation in vertebrate photoreceptors. Vision Res 1990; 30: 1923–48.

    Google Scholar 

  11. Hagins WA, Penn RD, Yoshikami S. Dark current and photocurrent in retinal rods. Biophys J 1970; 10: 380–412.

    Google Scholar 

  12. Penn RD, Hagins WA. Kinetics of the photocurrent of retinal rods. Biophys J 1972; 12: 1073–94.

    Google Scholar 

  13. Baylor DA, Lamb TB, Yau KW. The membrane current of single rod outer segments. J Physiol 1979; 288: 589–611.

    Google Scholar 

  14. Baylor DA, Nunn BJ, Schnapf JL. The photocurrent, noise and spectral sensitivity of rods of the monkey macaca fascicularis. J Physiol 1984; 357: 575–607.

    Google Scholar 

  15. Hood DC, Birch DG. The a-wave of the human electroretinogram and rod receptor function. Invest Ophthalmol Vis Sci 1990; 31: 2070–81.

    Google Scholar 

  16. Hood DC, Birch DG. A computational model of the amplitude and implicit time of the b-wave of the human ERG. Vis Neurosci. 1992; 8: 107–26.

    Google Scholar 

  17. Peachey NS, Alexander KR, Fishman GA. The luminance-response function of the dark-adapted human electroretinogram. Vision Res 1989; 29: 263–70.

    Google Scholar 

  18. Sieving PA, Nino C. Scotopic threshold response (STR) of the human electroretinogram. Invest Ophthalmol Vis Sci 1988; 11: 1608–14.

    Google Scholar 

  19. Brown KT, Murakami M. A new receptor potential of the monkey retina with no detectable latency. Nature 1964; 201: 626–8.

    Google Scholar 

  20. Brindley GS, Gardner-Medwin AR. The origin of the early receptor potential of the retina. J Physiol 1966; 182: 185–94.

    Google Scholar 

  21. Birch DG, Fish GE. Rod ERGs in retinitis pigmentosa and cone-rod degeneration. Invest Ophthalmol Vis Sci 1987; 28: 140–50.

    Google Scholar 

  22. Wyszecki G, Stiles WS. Color science. Concepts and methods, quantitative data and formulas. New York: John Wiley & Sons, 1982: 104.

    Google Scholar 

  23. Pugh EN Jr. Vision. Physics and retinal physiology. In: Atkinson RC, Herrnstein RJ, Lindzey G, Luce RD, eds. Stevens' handbook of experimental psychology. New York: John Wiley & Sons, 1988: 75–87.

    Google Scholar 

  24. Cobbs WH, Pugh EN Jr. Kinetics and components of the flash photocurrent of isolated retinal rods of the larval salamander, Ambystoma tigrinum. J Physiol 1987; 394: 529–72.

    Google Scholar 

  25. Newman EA, Odette LL. Model of electroretinogram b-wave generation. A test of the K+ hypothesis. Neurophysiol 1984; 51: 164–82.

    Google Scholar 

  26. Rodieck RW. The vertebrate retina. Principles of structure and function. San Francisco: W. H. Freeman and Co., 1973: 526–58.

    Google Scholar 

  27. Johnson MA, Massof RW. The photomyoclonic reflex. An artifact in the clinical electroretinogram. Br Ophthalmol 1988; 66: 368–78.

    Google Scholar 

  28. Montzka DP, Breton ME, Schueller AW. Cone intrusion in white and blue flash ERG a-wave velocity measurements [Abstract]. Invest Ophthalmol Vis Sci 1991; 32: 928.

    Google Scholar 

  29. Hood DC, Birch DG. A quantitative measure of the electrical activity of human rod photoreceptors using electroretinography. Vis Neurosci 1990; 5: 379–87.

    Google Scholar 

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Supported in part by a grant from the Ethel Brown Foerderer Foundation, Children's Hospital of Philadelphia, and by a grant from the Nina and Paul MacKall Trust.

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Breton, M.E., Montzka, D.P. Empiric limits of rod photocurrent component underlying a-wave response in the electroretinogram. Doc Ophthalmol 79, 337–361 (1992). https://doi.org/10.1007/BF00160948

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