| First Author | Herring A | Year | 2016 |
| Journal | Neurobiol Dis | Volume | 94 |
| Pages | 44-54 | PubMed ID | 27312772 |
| Mgi Jnum | J:259413 | Mgi Id | MGI:6141261 |
| Doi | 10.1016/j.nbd.2016.06.003 | Citation | Herring A, et al. (2016) Late running is not too late against Alzheimer's pathology. Neurobiol Dis 94:44-54 |
| abstractText | In the last decade a vast number of animal studies have produced overwhelming evidence that exercise not only compensates for memory loss by increasing brain plasticity and cognitive reserve but also directly counteracts Alzheimer-like pathology when provided before disease onset or in early disease stages. But so far, there is little knowledge about therapeutic effects of training when started in advanced disease stages. In the present study we show that following seven months of sedentary life style five months of wheel running, started four months after disease onset was still able to mitigate at least some aspects of the full-blown Alzheimer''s pathology in TgCRND8 mice. Late running had mild but significant effects on structural plasticity by increasing the dendritic complexity. It further reduced beta-amyloid (Abeta) plaque burden and enhanced Abeta clearance across the blood-brain barrier, along with attenuating microgliosis, inflammation, oxidative stress, and autophagy deficits, resulting in better memory performance and less agitation. However, unlike early exercise, late running did not affect abnormal amyloid precursor protein metabolism, tau pathology, or angiogenesis. These results allow concluding that it is never too late to counteract Alzheimer''s disease with physical training but the earlier the intervention starts, the more pronounced is the therapeutic potential. |
