Source:http://linkedlifedata.com/resource/pubmed/id/14550405
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2003-10-10
|
pubmed:abstractText |
Our purpose was to investigate the physiological phenotype of albino mice with a variation in the Rpe65 gene encoding either methionine or leucine at amino acid #450. Full-field electroretinograms (ERGs) were recorded from C57BL/6J-c(2J) albino mice with MET450 and BALB/cByJ albino mice with LEU450. Recordings from pigmented mice (C57BL/6J) served as controls. Rod ERG a-waves were fitted with a model to estimate parameters of activation. Recovery of function following a photobleach was studied by monitoring the return to pre-bleach a- or b-wave amplitudes of the dark-adapted electroretinogram. The parameter, S, derived from the fit of the rod model, was significantly higher for albino mice compared to pigmented controls. Between the albino mice, S was highest for BALB/cByJ compared to C57BL/6J-c(2J). The parameters t(d) and Rm(P3) were not different across the three strains. The difference in S between the BALB/cByJ and C57BL/6J-c(2J) albino strains is interpreted to reflect differences in intrinsic phototransduction gain. Recovery from a photobleach was also slower for the C57BL/6J-c(2J) albino mice compared with BALB/cByJ albino mice, consistent with prior studies showing slowed rhodopsin regeneration in mice with the RPE65-METH450 variant. ERG recordings show that C57BL/6J-c(2J) albino mice with the MET450 variant of the RPE65 protein have a lower gain of activation and slower recovery from photobleach than do the BALB/cByJ albino mice with LEU450. Both the slower recovery from photobleach and lower gain of activation characteristic of the C57BL/6J-c(2J) strain may contribute to the mechanism by which it is protected from light-induced photoreceptor death relative to BALB/c.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0014-4835
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
77
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
627-38
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:14550405-Albinism, Ocular,
pubmed-meshheading:14550405-Animals,
pubmed-meshheading:14550405-Carrier Proteins,
pubmed-meshheading:14550405-Electroretinography,
pubmed-meshheading:14550405-Eye Proteins,
pubmed-meshheading:14550405-Genetic Predisposition to Disease,
pubmed-meshheading:14550405-Mice,
pubmed-meshheading:14550405-Mice, Inbred BALB C,
pubmed-meshheading:14550405-Mice, Inbred C57BL,
pubmed-meshheading:14550405-Phenotype,
pubmed-meshheading:14550405-Photobleaching,
pubmed-meshheading:14550405-Proteins,
pubmed-meshheading:14550405-Recovery of Function,
pubmed-meshheading:14550405-Species Specificity,
pubmed-meshheading:14550405-Vision, Ocular
|
pubmed:year |
2003
|
pubmed:articleTitle |
Electroretinographic evidence for altered phototransduction gain and slowed recovery from photobleaches in albino mice with a MET450 variant in RPE65.
|
pubmed:affiliation |
Jules Stein Eye Institute, UCLA Medical Center, 100 Stein Plaza, Los Angeles, CA 90095, USA. nusinowitz@jsei.ucla.edu
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|