| First Author | Whyte LS | Year | 2018 |
| Journal | Behav Brain Res | Volume | 336 |
| Pages | 177-181 | PubMed ID | 28887197 |
| Mgi Jnum | J:250583 | Mgi Id | MGI:6095016 |
| Doi | 10.1016/j.bbr.2017.09.006 | Citation | Whyte LS, et al. (2018) Reduction in open field activity in the absence of memory deficits in the App(NL-G-F) knock-in mouse model of Alzheimer's disease. Behav Brain Res 336:177-181 |
| abstractText | The recent development of knock-in mouse models of Alzheimer's disease provides distinct advantages over traditional transgenic mouse models that rely on over-expression of amyloid precursor protein. Two such knock-in models that have recently been widely adopted by Alzheimer's researchers are the App(NL-F) and App(NL-G-F) mice. This study aimed to further characterise the behavioural phenotype and amyloid plaque distribution of App(NL-G-F/NL-G-F) (C57BL/6J background) mice at six-months of age. An attempt to replicate a previous study that observed deficits in working memory in the Y-maze, showed no difference between App(NL-G-F/NL-G-F) and wild-type mice. Further assessment of these mice using the novel object recognition test and Morris water maze also revealed no differences between App(NL-G-F/NL-G-F) and wild-type mice. Despite a lack of demonstrated cognitive deficits, we report a reduction in locomotor/exploratory activity in an open field. Histological examination of App(NL-G-F/NL-G-F) mice showed widespread distribution of amyloid plaques at this age. We conclude that whilst at six-months of age, memory deficits are not sufficiently robust to be replicated in varying environments, amyloid plaque burden is significant in App(NL-G-F/NL-G-F) knock-in brain. |
