| First Author | Dumont M | Year | 2011 |
| Journal | FASEB J | Volume | 25 |
| Issue | 11 | Pages | 4063-72 |
| PubMed ID | 21825035 | Mgi Jnum | J:178410 |
| Mgi Id | MGI:5298309 | Doi | 10.1096/fj.11-186650 |
| Citation | Dumont M, et al. (2011) Behavioral deficit, oxidative stress, and mitochondrial dysfunction precede tau pathology in P301S transgenic mice. FASEB J 25(11):4063-72 |
| abstractText | Abnormal tau accumulation can lead to the development of neurodegenerative diseases. P301S mice overexpress the human tau mutated gene, resulting in tau hyperphosphorylation and tangle formation. Mice also develop synaptic deficits and microglial activation prior to any neurodegeneration and tangles. Oxidative stress can also affect tauopathy. We studied the role of oxidative stress in relationship to behavioral abnormalities and disease progression in P301S mice at 2, 7, and 10 mo of age. At 7 mo of age, P301S mice had behavioral abnormalities, such as hyperactivity and disinhibition. At the same age, we observed increased carbonyls in P301S mitochondria ( approximately 215 and 55% increase, males/females), and deregulation in the activity and content of mitochondrial enzymes involved in reactive oxygen species formation and energy metabolism, such as citrate synthase ( approximately 19 and approximately 5% decrease, males/females), MnSOD ( approximately 16% decrease, males only), cytochrome C ( approximately 19% decrease, females only), and cytochrome C oxidase ( approximately 20% increase, females only). These changes in mitochondria proteome appeared before tau hyperphosphorylation and tangle formation, which were observed at 10 mo and were associated with GSK3beta activation. At that age, mitochondria proteome deregulation became more apparent in male P301S mitochondria. The data strongly suggest that oxidative stress and mitochondrial abnormalities appear prior to tau pathology. |
