behavior/neurological
• fail to show intersession habituation over 3 days of testing in an open field, unlike transgenic mice wild-type for Ldlr
|
• learning impairment in a Morris water maze at 10 months of age
• impairment not affected by Ldlr genotype
|
• at 13 months of age mice trained at 10 months of age are slower to reacquire the location of the hidden platform in a morris water maze compared to transgenic mice wild-type for Ldlr
• in a probe trial mice fail to occupy the target quadrant longer than chance indicating memory retention deficits
|
• make more entries into the open arms of an elevated plus maze on day 2 of testing
|
• relative to non-transgenic controls
|
homeostasis/metabolism
amyloidosis
(
J:114480
)
• age dependent cerebral amyloidosis
• plaques first appear in the hippocampus and cortex at around 11 months
• progressive accumulation in the brain after 11 months
|
• cerebral amyloid beta deposition is increased compared to transgenic mice wild-type for Ldlr
|
• hypercholesterolemia with the increase in the non-HDL fraction
|
• increase is mainly in the LDL fraction
|
nervous system
• cerebral amyloid beta deposition is increased compared to transgenic mice wild-type for Ldlr
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
Alzheimer's disease | DOID:10652 | J:114480 |