In-depth functional diagnostics of mouse models by single-flash and flicker electroretinograms without adapting background illumination
Electroretinograms (ERGs) are commonly recorded at the cornea for an assessment of the functional status of the retina in mouse models. Full-field ERGs can be elicited by single-flash as well as flicker light stimulation although in most laboratories flicker ERGs are recorded much less frequently th...
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| Main Authors: | , |
|---|---|
| Format: | Chapter/Article |
| Language: | English |
| Published: |
2016
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| In: |
Retinal Degenerative Diseases
Year: 2016, Pages: 619-625 |
| DOI: | 10.1007/978-3-319-17121-0_82 |
| Online Access: | Verlag, Volltext: http://dx.doi.org/10.1007/978-3-319-17121-0_82 |
| Author Notes: | Naoyuki Tanimoto, Stylianos Michalakis, Bernhard H. F. Weber, Christian A. Wahl-Schott, Hans-Peter Hammes, Mathias W. Seeliger |
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| 245 | 1 | 0 | |a In-depth functional diagnostics of mouse models by single-flash and flicker electroretinograms without adapting background illumination |c Naoyuki Tanimoto, Stylianos Michalakis, Bernhard H. F. Weber, Christian A. Wahl-Schott, Hans-Peter Hammes, Mathias W. Seeliger |
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| 520 | |a Electroretinograms (ERGs) are commonly recorded at the cornea for an assessment of the functional status of the retina in mouse models. Full-field ERGs can be elicited by single-flash as well as flicker light stimulation although in most laboratories flicker ERGs are recorded much less frequently than singleflash ERGs. Whereas conventional single-flash ERGs contain information about layers, i.e., outer and inner retina, flicker ERGs permit functional assessment of the vertical pathways of the retina, i.e., rod system, cone ON-pathway, and cone OFF-pathway, when the responses are evoked at a relatively high luminance (0.5 log cd s/m2) with varying frequency (from 0.5 to 30 Hz) without any adapting background illumination. Therefore, both types of ERGs complement an in-depth functional characterization of the mouse retina, allowing for a discrimination of an underlying functional pathology. Here, we introduce the systematic interpretation of the single-flash and flicker ERGs by demonstrating several different patterns of functional phenotype in genetic mouse models, in which photoreceptors and/or bipolar cells are primarily or secondarily affected. | ||
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| 650 | 4 | |a Electroretinogram | |
| 650 | 4 | |a Flicker | |
| 650 | 4 | |a Functional diagnostics | |
| 650 | 4 | |a Mouse model | |
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