Literature DB >> 8627418

Photoreceptor and bipolar cell contributions to the cat electroretinogram: a kinetic model for the early part of the flash response.

J G Robson1, L J Frishman.   

Abstract

The time course of the initial negative wave of the flash electroretinogram of the dark-adapted cat has been found to be critically dependent of contributions from cells of the inner retina, not only for very low-intensity flashes for which the negative scotopic threshold response is dominant but also when the stimulus is sufficiently intense for the rods themselves to contribute directly to the electroretinogram. However, if the inner-retinal responses are blocked pharmacologically or are suppressed by a steady adapting background, the initial negative wave of the remaining electroretinogram (the alpha wave) can be explained as the sum of photoreceptor and bipolar-cell components that can be modeled as described by Lamb and Pugh [J. Physiol. (London) 449, 717 (1992)] and Robson and Frishman [Vis. Neurosci. 12, 837 (1995)], respectively.

Mesh:

Year:  1996        PMID: 8627418     DOI: 10.1364/josaa.13.000613

Source DB:  PubMed          Journal:  J Opt Soc Am A Opt Image Sci Vis        ISSN: 1084-7529            Impact factor:   2.129


  38 in total

1.  Electroretinographic determination of human rod flash response in vivo.

Authors:  D R Pepperberg; D G Birch; D C Hood
Journal:  Methods Enzymol       Date:  2000       Impact factor: 1.600

2.  Contribution of cone photoreceptors and post-receptoral mechanisms to the human photopic electroretinogram.

Authors:  C Friedburg; C P Allen; P J Mason; T D Lamb
Journal:  J Physiol       Date:  2004-02-27       Impact factor: 5.182

3.  Modelling the initial phase of the human rod photoreceptor response to the onset of steady illumination.

Authors:  Omar A R Mahroo; Vin Shen Ban; Benjamin M Bussmann; Hannah C Copley; Christopher J Hammond; Trevor D Lamb
Journal:  Doc Ophthalmol       Date:  2012-02-19       Impact factor: 2.379

4.  A(max) is the best a-wave measure for classifying Abyssinian cat rod/cone dystrophy.

Authors:  Kristina Narfström
Journal:  Doc Ophthalmol       Date:  2006-02-25       Impact factor: 2.379

5.  Partial rescue of retinal function and sterol steady-state in a rat model of Smith-Lemli-Opitz syndrome.

Authors:  Steven J Fliesler; Dana K Vaughan; Erin C Jenewein; Michael J Richards; Barbara A Nagel; Neal S Peachey
Journal:  Pediatr Res       Date:  2007-03       Impact factor: 3.756

6.  The cone electroretinogram in retinopathy of prematurity.

Authors:  Anne B Fulton; Ronald M Hansen; Anne Moskowitz
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-02       Impact factor: 4.799

7.  Cone ERG responses in patients with Smith-Lemli-Opitz Syndrome (SLOS).

Authors:  Deirdre Garry; Ronald M Hansen; Anne Moskowitz; Ellen R Elias; Mira Irons; Anne B Fulton
Journal:  Doc Ophthalmol       Date:  2010-05-04       Impact factor: 2.379

8.  Contribution of voltage-gated sodium channels to the b-wave of the mammalian flash electroretinogram.

Authors:  Deb Kumar Mojumder; David M Sherry; Laura J Frishman
Journal:  J Physiol       Date:  2008-04-03       Impact factor: 5.182

9.  Rod and rod-driven function in achromatopsia and blue cone monochromatism.

Authors:  Anne Moskowitz; Ronald M Hansen; James D Akula; Susan E Eklund; Anne B Fulton
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-09-29       Impact factor: 4.799

10.  Dimethyl sulphoxide dose-response on rat retinal function.

Authors:  Tina I Tsai; Bang V Bui; Algis J Vingrys
Journal:  Doc Ophthalmol       Date:  2009-09-11       Impact factor: 2.379

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