Literature DB >> 19760280

Electrophysiological deficits in the retina of the DBA/2J mouse.

Joanna Harazny1, Michael Scholz, Thomas Buder, Berthold Lausen, Jan Kremers.   

Abstract

The DBA/2J (D2J) is a genetic mouse model for glaucomatous neurodegeneration because the animals develop anatomical and functional retinal deficits that partially can be correlated with elevated intraocular pressure (IOP). The IOP starts to increase at an age of about 6 months as a result of morphological changes within the anterior eye segment, e.g., pigment dispersion and iris synechiae. The purpose of the present study was to investigate how ERG responses change in individuals at different ages in D2J mice and to compare these changes with normal aging effects in pigmented C57/B6 (B6) mice. IOP was measured in awake, non-sedated D2J and B6 mice with a rebound tonometer. At ages between 2-3 and 10 months, scotopic flash ERGs were measured five times with about 2 months' intervals. In addition, light adapted flicker ERGs were recorded. Our data show that the D2J shows lower flicker ERG responses than the B6 mice already at an age of 2-3 months. Dark adapted flash ERG responses are not decreased at this age. In both mouse strains the ERG responses decrease as a function of age, but there is a stronger decrease in the D2J mice. The data of flicker ERGs suggest the presence of early functional deficits in the D2J retina that possibly have a post-receptoral origin. The scotopic flash ERG reveals a functional deficit that occurs at a later stage and that possibly is IOP dependent. But, the deficits appear at an age at which the IOP is still lower than in the B6 mouse, indicating that other factors play an additional role.

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Year:  2009        PMID: 19760280     DOI: 10.1007/s10633-009-9194-5

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


  31 in total

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5.  Method for the noninvasive measurement of intraocular pressure in mice.

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7.  Longitudinal evaluation of retinal ganglion cell function and IOP in the DBA/2J mouse model of glaucoma.

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8.  The number of people with glaucoma worldwide in 2010 and 2020.

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9.  Dependency of intraocular pressure elevation and glaucomatous changes in DBA/2J and DBA/2J-Rj mice.

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10.  Retinal ganglion cell degeneration is topological but not cell type specific in DBA/2J mice.

Authors:  Tatjana C Jakobs; Richard T Libby; Yixin Ben; Simon W M John; Richard H Masland
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3.  A Multiple Piccolino-RIBEYE Interaction Supports Plate-Shaped Synaptic Ribbons in Retinal Neurons.

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Review 6.  Psychophysical testing in rodent models of glaucomatous optic neuropathy.

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7.  Loss of outer retinal neurons and circuitry alterations in the DBA/2J mouse.

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8.  Effect of general anesthetics on IOP in elevated IOP mouse model.

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9.  The age-regulating protein klotho is vital to sustain retinal function.

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10.  Quantification of Changes in Visual Function During Disease Development in a Mouse Model of Pigmentary Glaucoma.

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