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Erschienen in: Documenta Ophthalmologica 3/2014

01.06.2014 | Original Research Article

Contribution of retinal ganglion cells to the mouse electroretinogram

verfasst von: Benjamin J. Smith, Xu Wang, Balwantray C. Chauhan, Patrice D. Côté, François Tremblay

Erschienen in: Documenta Ophthalmologica | Ausgabe 3/2014

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Abstract

Purpose

To quantify the direct contribution of retinal ganglion cells (RGCs) on individual components of the mouse electroretinogram (ERG).

Methods

Dark- and light-adapted ERGs from mice 8 to 12 weeks after optic nerve transection (ONTx, n = 14) were analyzed through stimulus response curves for a- and b-waves, oscillatory potentials (OPs), positive and negative scotopic threshold response (p/n STR), and the photopic negative response (PhNR) and compared with unoperated and sham-operated controls, as well as to eyes treated with 6-cyano-7-nitroquinoxaline-2,3-dion (CNQX).

Results

We confirmed in mice that CNQX intravitreal injection reduced the scotopic a-wave amplitude at high flash strength, confirming a post-receptoral contribution to the a-wave. We found that ONTx, which is more specific to RGCs, did not affect the a-wave amplitude and implicit time in either photopic or scotopic conditions while the b-wave was reduced. Both the pSTR and nSTR components were reduced in amplitude, with the balance between the two components resulting in a shortening of the nSTR peak implicit time. On the other hand, amplitude of the PhNR was increased while the OPs were minimally affected.

Conclusion

With an intact a-wave demonstrated following ONTx, we find that the most robust indicators of RGC function in the mouse full-field ERG were the STR components.
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Metadaten
Titel
Contribution of retinal ganglion cells to the mouse electroretinogram
verfasst von
Benjamin J. Smith
Xu Wang
Balwantray C. Chauhan
Patrice D. Côté
François Tremblay
Publikationsdatum
01.06.2014
Verlag
Springer Berlin Heidelberg
Erschienen in
Documenta Ophthalmologica / Ausgabe 3/2014
Print ISSN: 0012-4486
Elektronische ISSN: 1573-2622
DOI
https://doi.org/10.1007/s10633-014-9433-2

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