Literature DB >> 33063285

Relationship between stimulus size and different components of the electroretinogram (ERG) elicited by flashed stimuli.

Mathias G Nittmann1, Avinash J Aher2, Jan Kremers2,3,4, Radouil Tzekov5,6,7,8,9.   

Abstract

PURPOSE: To investigate how light stimulus conditions of varying spatial sizes affect components of the flash and long-flash electroretinogram (ERG) in normal subjects.
METHOD: Three stimulus conditions were generated by a Ganzfeld stimulator: a white flash on white background (WoW), a red flash on a blue background (RoB) and an L+M-cone isolating on-off (long flash) stimulus (Cone Iso). ERGs were recorded from six subjects (5 M, 1 F) with DTL electrodes to full-field (FF), 70°, 60°, 50°, 40°, 30° and 20° diameter circular stimuli. Amplitudes and peak times for a-, b-, d- and i-wave, and PhNR were examined. PhNR amplitudes were estimated in two different ways: from baseline (fB) and from preceding b-wave peak (fP).
RESULTS: With decreasing stimulus size, amplitudes for all ERG waveform components attenuated and peak times increased, although the effect varied across different components. An exponential fit described the relationship between amplitudes and size of stimulated retinal area well for most components and conditions (R2= 0.75-0.99), except for PhNR(fB) (R2= - 0.16-0.88). For peak times, an exponential decay function also fitted the data well (R2= 0.81-0.97), except in a few cases where the exponential constant was too small and a linear regression function was applied instead (a-wave Cone Iso, b- and i-wave WoW). The exponential constants for RoB amplitudes (b-wave, PhNR(fB), PhNR(fP)) were larger compared to their counterparts under WoW (p < 0.05), while there was no difference between the constants for a-wave amplitudes and peak times and for PhNR peak times. The exponential constants of amplitudes vs. area under WoW and Cone Iso were remarkably similar, while under RoB PhNR(fB) showed larger constants compared to either a- or b-wave (p < 0.05).
CONCLUSION: ERG components change in a predictable way with stimulus size and spectral characteristics of the stimulus under these conditions. This predictability could allow a modified version of these sets of stimuli to be tested for clinical applicability.

Entities:  

Keywords:  Electroretinogram; Flash stimuli; Photopic negative response; Square wave stimuli; Stimulus size

Mesh:

Year:  2020        PMID: 33063285     DOI: 10.1007/s10633-020-09797-6

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  41 in total

1.  Contribution to the kinetics and amplitude of the electroretinogram b-wave by third-order retinal neurons in the rabbit retina.

Authors:  C J Dong; W A Hare
Journal:  Vision Res       Date:  2000       Impact factor: 1.886

2.  Effects of Spectral Characteristics of Ganzfeld Stimuli on the Photopic Negative Response (PhNR) of the ERG.

Authors:  Nalini V Rangaswamy; Suguru Shirato; Muneyoshi Kaneko; Beth I Digby; John G Robson; Laura J Frishman
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-10       Impact factor: 4.799

3.  ISCEV Standard for full-field clinical electroretinography (2015 update).

Authors:  Daphne L McCulloch; Michael F Marmor; Mitchell G Brigell; Ruth Hamilton; Graham E Holder; Radouil Tzekov; Michael Bach
Journal:  Doc Ophthalmol       Date:  2014-12-14       Impact factor: 2.379

4.  The photopic negative response of the flash electroretinogram in primary open angle glaucoma.

Authors:  S Viswanathan; L J Frishman; J G Robson; J W Walters
Journal:  Invest Ophthalmol Vis Sci       Date:  2001-02       Impact factor: 4.799

5.  A proximal retinal component in the primate photopic ERG a-wave.

Authors:  R A Bush; P A Sieving
Journal:  Invest Ophthalmol Vis Sci       Date:  1994-02       Impact factor: 4.799

6.  Photopic negative response of the human ERG: losses associated with glaucomatous damage.

Authors:  A Colotto; B Falsini; T Salgarello; G Iarossi; M E Galan; L Scullica
Journal:  Invest Ophthalmol Vis Sci       Date:  2000-07       Impact factor: 4.799

7.  Selective loss of the photopic negative response in patients with optic nerve atrophy.

Authors:  Yasutaka Gotoh; Shigeki Machida; Yutaka Tazawa
Journal:  Arch Ophthalmol       Date:  2004-03

8.  Photopic ERGs in patients with optic neuropathies: comparison with primate ERGs after pharmacologic blockade of inner retina.

Authors:  Nalini V Rangaswamy; Laura J Frishman; E Ulysses Dorotheo; Jade S Schiffman; Hasan M Bahrani; Rosa A Tang
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-10       Impact factor: 4.799

9.  Rod and cone contributions to the a-wave of the electroretinogram of the macaque.

Authors:  John G Robson; Shannon M Saszik; Jameel Ahmed; Laura J Frishman
Journal:  J Physiol       Date:  2003-01-24       Impact factor: 5.182

10.  Luminance dependence of neural components that underlies the primate photopic electroretinogram.

Authors:  Shinji Ueno; Mineo Kondo; Yasuhiro Niwa; Hiroko Terasaki; Yozo Miyake
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-03       Impact factor: 4.799

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