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Neurofibrillary tangles and senile plaques in aged bears
L C Cork1, R E Powers, D J Selkoe
1Division of Comparative Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2182.
Journal of Neuropathology and Experimental Neurology
|November 1, 1988
Summary
Aged bears develop brain changes like those seen in human Alzheimer's disease (AD). Researchers found neurofibrillary tangles (NFT) and senile plaques (SP) in bears, suggesting shared aging pathways.
Area of Science:
- Comparative pathology
- Neuroscience
- Gerontology
Background:
- Aging humans and Alzheimer's disease (AD) patients exhibit neuronal cytoskeletal abnormalities, including neurofibrillary tangles (NFT) and senile plaques (SP).
- While SP are found in various species, NFT with human-like characteristics have not been previously identified in non-human mammals.
Purpose of the Study:
- To investigate the presence of age-related cytoskeletal abnormalities in nonprimate mammals, specifically aged bears.
- To compare the pathological findings in bears with those observed in human aging and Alzheimer's disease.
Main Methods:
- Examination of brain tissue from five aged bears (20-30 years old).
- Immunocytochemical analysis using antibodies against phosphorylated neurofilaments (NF), tau, A68 (AD-associated protein), and paired helical filament (PHF) antigen.
- Histopathological assessment for the presence of NFT and SP.
Main Results:
- An aged Asiatic brown bear exhibited NFT composed of 10-16 nm filaments, immunoreactive to antibodies for phosphorylated NF, tau, A68, and PHF antigen.
- An aged polar bear presented numerous SP with neurites immunoreactive to phosphorylated NF antibodies, but without identified NFT.
- These findings demonstrate age-related cytoskeletal abnormalities in nonprimate species.
Conclusions:
- Nonprimate mammals, such as bears, can develop age-related cytoskeletal abnormalities analogous to those in humans.
- Comparative pathology studies in aged mammals offer a valuable model for understanding the pathogenesis of neurodegenerative changes.
- Further research into comparative mammalian pathology may illuminate mechanisms underlying age-associated neurological disorders.