| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1934730 | Biochemical and Biophysical Research Communications | 2009 | 5 Pages |
Aging is the greatest risk factor for neurodegenerative diseases such as Alzheimer’s disease (AD). Age-dependent alterations of cell signaling play an important role in the onset of AD. The serine/threonine kinase Akt is a critical cell signaling to neuronal survival. Using the senescence-accelerated mouse SAMP10, we investigated the effect of aging on AKT signaling in hippocampus tissue. During aging, the expression of Akt mRNA and protein remained stable. However, the constructive phosphorylation of AktSer473 displayed a continuous decrease after 6 months in SAMP10. When compared with the control SAMR1, aged SAMP10 mice showed significant reduced phosphorylation of AktSer473. SAMP10 at the age of 6 months showed obvious deterioration in performance of learning and memory tasks. Thus, the data reported here suggested a potential link between the age-related alteration of AktSer473 and the deterioration in performance of learning and memory tasks in SAMP10 mouse.
