Abstract
In aged human beings and in individuals with age-associated degenerative disorders, particularly Alzheimer’s disease (AD), neurons develop cytoskeletal abnormalities, including neurofibrillary tangles (NFT) and senile plaques (SP). Senile plaques occur in several nonhuman species; however, NFT, with ultrastructural or immunocytochemical similarities to those occurring in humans, have not been identified in other mammals. In this study of five aged bears (Ursus, 20-30 years of age), we identified cytoskeletal abnormalities similar to those occurring in humans. An aged Asiatic brown bear had NFT, composed of straight 10-16-nm filaments, that were immunoreactive with antibodies directed against: phosphorylated epitopes of neurofilaments (NF); tau; A68 (a protein enriched in AD); and an antigen associated with paired helical filaments (PHF). An aged polar bear had numerous SP; neurites of these plaques were immunoreactive with antibodies against phosphorylated epitopes of NF, but NFT were not identified. These results indicate that nonprimate species develop age-related cytoskeletal abnormalities similar to those occurring in humans. Investigations of the comparative pathology of aged mammals may be useful in elucidating the pathogeneses of these abnormalities.
Original language | English (US) |
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Pages (from-to) | 629-641 |
Number of pages | 13 |
Journal | Journal of neuropathology and experimental neurology |
Volume | 47 |
Issue number | 6 |
DOIs | |
State | Published - Nov 1988 |
Keywords
- Aging
- Alzheimer’s disease
- Cytoskeleton
- Hippocampus
ASJC Scopus subject areas
- Medicine(all)