Abstract
In response to progressively stronger flashes delivered against a rod saturating background light, the amplitude of the photopic ERG b-wave first increases, reaches a maximal value (V max) and then decreases gradually to a plateau where the amplitude of the b-wave equals that of the a-wave, a phenomenon known as the photopic hill (PH). The purpose of this study was to investigate how the PH grew during the course of the light adaptation (LA) process that follows a period of dark adaptation (DA): the so-called light adaptation effect (LAE). Photopic ERG (time-integrated) luminance-response (LR) functions were obtained prior to (control-fully light adapted) and at 0, 5 and 10 min of LA following a 30-min period of DA. A mathematical model combining a Gaussian and a logistic growth function, suggested to reflect the OFF and ON retinal contribution to the PH respectively, was fitted to the LR functions thus obtained. Our results indicate that the magnitude of the cone ERG LAE is modulated by the stimulus luminance, with b-wave enhancements being maximal for luminance levels that result in the descent of the PH. The Gaussian function grew significantly with LA while the logistic growth function remained basically unchanged. Our findings would therefore suggest that the LAE reflects primarily an increase in the retinal OFF response during LA.
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References
Lachapelle P (1987) Analysis of the photopic electroretinogram recorded before and after dark adaptation. Can J Ophthalmol 22:354–361
Gouras P, MacKay CJ (1989) Growth in amplitude of the human cone electroretinogram with light adaptation. Invest Ophthalmol Vis Sci 30:625–630
Peachey NS, Alexander KR, Fishman GA (1991) Visual adaptation and the cone flicker electroretinogram. Invest Ophthalmol Vis Sci 32:1517–1522
Peachey NS, Alexander KR, Derlacki DJ, Bobak P, Fishman GA (1991) Effects of light adaptation on the response characteristics of human oscillatory potentials. Electroencephalogr Clin Neurophysiol 78:27–34
Murayama K, Sieving PA (1992) Different rates of growth of monkey and human photopic a-, b- and d-waves suggest two sites of ERG light adaptation. Clin Vis Sci 7:385–392
Armington JC, Biersdorf WR (1958) Long-term light adaptation of the human electroretinogram. J Comp Physiol Psychol 51:1–5
Weleber RG, Eisner A (1992) Retinal function and physiological studies. In: Newsome DA (ed) Retinal dystrophies and degenerations. Raven Press, New York, pp 21–83
Peachey NA, Arakawa K, Alexander KR, Marchese AL (1992) Rapid and slow changes in the human cone electroretinogram during light and dark adaptation. Vision Res 32:2049–2053
Burian HM (1954) Electric responses of the human visual system. Arch Ophthalmol 51:509–524
Bui BV, Fortune B (2006) Origin of electroretinogram amplitude growth during light adaptation in pigmented rats. Vis Neurosci 23:155–167
Alexander LR, Raghuram A, Rajagopalan AS (2006) Cone phototransduction and growth of the ERG b-wave during light adaptation. Vision Res 46:3941–3948
Benoit J, Lachapelle P (1995) Light adaptation of the human photopic oscillatory potentials: influence of the length of the dark adaptation period. Doc Ophthalmol 89:267–276
Rousseau S, Lachapelle P (2000) Transient enhancing of cone electroretinograms following exposure to brighter photopic backgrounds: a new light adaptation effect. Vision Res 40:1013–1018
Wali N, Leguire LE (1992) The photopic hill: a new phenomenon of the light adapted electroretinogram. Doc Ophthalmol 80:335–345
Kondo M, Piao CH, Tanikawa A, Horiguchi M, Terasaki H, Miyake Y (2000) Amplitude decrease of photopic ERG b-wave at higher stimulus intensities in humans. Jpn J Ophthalmol 44:20–28
Rufiange M, Rousseau S, Dembinska O, Lachapelle P (2002) Cone-dominated ERG luminance-response function: the Photopic Hill revisited. Doc Ophthalmol 104:231–248
Rufiange M, Dumont M, Lachapelle P (2002) Correlating retinal function with melatonin secretion in subjects with an early or late circadian phase. Invest Ophthalmol Vis Sci 43:2491–2499
Rufiange M, Dassa J, Dembinska O, Koenekoop RK, Little JM, Polomeno RC, Dumont M, Chemtob S, Lachapelle P (2003) The photopic ERG luminance-response function (photopic hill): method of analysis and clinical application. Vision Res 43:1405–1412
Ueno S, Kondo M, Niwa S, Terasaki H, Miyake Y (2004) Luminance dependence of neural components that underlies the primate photopic electroretinogram. Invest Ophthalmol Vis Sci 45:1033–1040
Rufiange M, Dumont M, Lachapelle P (2005) Modulation of the human photopic ERG luminance-response function with the use of chromatic stimuli. Vision Res 45:2321–2330
Hamilton R, Bees MA, Chaplin CA, McCulloch DL (2007) The luminance-response function of the human photopic electroretinogram: a mathematical model. Vision Res 47:2968–2972
Marmor MF, Fulton AB, Holder GE, Miyake Y, Brigell M, Bach M, International Society for Clinical Electrophysiology of Vision (2009) ISCEV Standard for full-field clinical electroretinography (2008 update). Doc Ophthalmol 118:69–77
McCulloch DL, Hamilton R (2010) Essentials of photometry for clinical electrophysiology of vision. Doc Ophthalmol 121:77–84
Bush RA, Sieving PA (1994) A proximal retinal component in the primate photopic ERG a-wave. Invest Ophthalmol Vis Sci 35:635–645
Rangaswamy NV, Hood DC, Frishman LJ (2003) Regional variations in local contributions to the primate photopic flash ERG: Revealed using the slow-sequence mfERG. Invest Ophthalmol Vis Sci 44:3233–3247
Beaulieu C, Rufiange M, Dumont M, Lachapelle P (2009) Modulation of ERG retinal sensitivity parameters with light environment and photoperiod. Doc Ophthalmol 118:89–99
Birch DG, Fish GE (1987) Rod ERGs in retinitis pigmentosa and cone-rod degeneration. Invest Ophthalmol Vis Sci 28:140–150
Lachapelle P (1990) Oscillatory potentials as predictors to amplitude and peak time of the photopic b-wave of the human electroretinogram. Doc Ophthalmol 75:73–82
Lachapelle P (1991) Evidence for an intensity-coding oscillatory potential in the human electroretinogram. Vis Res 31:767–774
Nagata M (1963) Studies on the photopic ERG of the human retina. Jpn J Ophthalmol 7:96–124
Kojima M, Zrenner E (1978) OFF-components in response to brief light flashes in the oscillatory potential of the human electroretinogram. Albrecht Von Graefes Arch Clin Exp Ophthalmol 206:107–120
Miyake Y, Yagasaki K, Horigushi M, Kawase Y (1987) ON- and OFF-responses in photopic electroretinogram in complete and incomplete types of congenital stationary night blindness. Jpn J Ophthalmol 31:81–87
Nakajima Y, Iwakabe H, Akazawa C, Naka H, Shigemoto R, Mizuno N, Nakanishi S (1993) Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4-phosphonobutyrate. J Biol Chem 268:11868–11873
Quigley M, Roy MS, Barsoum-Homsy M, Chevrette L, Jacob JL, Milot J (1996–1997) ON- and OFF-responses in the photopic electroretinogram in complete-type congenital stationary night blindness. Doc Ophthalmol 92:159-165
Lachapelle P, Rousseau S, McKerral M, Benoit J, Polomeno RC, Koenekoop RK, Little JM (1998) Evidence supportive of a functional discrimination between photopic oscillatory potentials as revealed with cone and rod mediated retinopathies. Doc Ophthalmol 95:35–54
Bech-Hansen NT, Naylor MJ, Maybaum TA, Sparkes RL, Koop B, Birch DG, Bergen AA, Prinsen CF, Polomeno RC, Gal A, Drack AV, Musarella MA, Jacobson SG, Young RS, Weleber RG (2000) Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Nat Genet 26:319–323
Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E (2002) Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type. Vis Res 42:1475–1483
Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, Derlacki DJ, Rajagopalan AS (2005) Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. Proc Natl Acad Sci USA 102:4884–4889
Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Matyas G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W (2005) Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. Invest Ophthalmol Vis Sci 46:4328–4335
Morgans CW, Ren G, Akileswaran L (2006) Localization of nyctalopin in the mammalian retina. Eur J Neurosci 23:1163–1171
Miyake Y, Horiguchi M, Ota I, Shiroyama N (1987) Characteristic ERG flicker anomaly in incomplete congenital stationary night blindness. Invest Ophthalmol Vis Sci 28:1816–1823
Acknowledgments
This study was supported by McGill University-Montreal Children’s Hospital Research Institute, the Canadian Institute for Health Research, the Foundation Fighting Blindness (USA) and FRSQ-Réseau-Vision.
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Garon, ML., Rufiange, M., Hamilton, R. et al. Asymmetrical growth of the photopic hill during the light adaptation effect. Doc Ophthalmol 121, 177–187 (2010). https://doi.org/10.1007/s10633-010-9243-0
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DOI: https://doi.org/10.1007/s10633-010-9243-0