Development of amyloid burden in African Green monkeys
Open accessAbstract
The vervet is an old world monkey increasingly being used as a model for human diseases. In addition to plaques and tangles, an additional hallmark of Alzheimer's disease is damage to neurons that synthesize noradrenaline (NA). We characterized amyloid burden in the posterior temporal lobe of young and aged vervets, and compared that with changes in NA levels and astrocyte activation. Total amyloid beta (Aβ)40 and Aβ42 levels were increased in the aged group, as were numbers of amyloid plaques detected using antibody 6E10. Low levels of Aβ42 were detected in 1 of 5 younger animals, although diffusely stained plaques were observed in 4 of these. Increased glial fibrillary acidic protein staining and messenger RNA levels were significantly correlated with increased age, as were cortical NA levels. Levels of Aβ42 and Aβ40, and the number of 6E10-positive plaques, were correlated with NA levels. Interestingly messenger RNA levels of glial derived neurotrophic factor, important for noradrenergic neuronal survival, were reduced with age. These findings suggest that amyloid pathology in aged vervets is associated with astrocyte activation and higher NA levels.
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Vervets have evidence of Aβ deposition, gliosis and neuronal dystrophy with age.
“Vervets live to approximately 30 years in captivity and have evidence of Aβ deposition, gliosis and neuronal dystrophy with age [72, 88, 89].”
From Alzheimer's disease: experimental models and reality (2017) · cites this paper as [72]
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Neuropathology and Biomarker Correlates of Late Onset Alzheimer’s Disease in Aged Old World Monkeys
Zeiss, C. J., Duque, A., & Huttner, A. J. (2025) · Toxicologic Pathology · doi:10.1177/01926233251388069 · Cited by 2 · see citing works
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Self-citationKrizan, I. M., Sai, K. K. S., Damuka, N., Macauley, S. L., Thurman, B. M., Long, M., & Kavanagh, K. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4821607
- Authors
- Kalinin, S., Willard, S. L., Shively, C. A., Kaplan, J. R., Register, T. C., Jorgensen, M. J., Polak, P. E., Rubinstein, I., & Feinstein, D. L.
- Affiliations
- University of Illinois Chicago (US)
- Wake Forest University Health Sciences (US)
- Corresponding author
- Feinstein, Douglas L.
- ORCID
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2013-10
- Volume
- 34
- Issue
- 10
- Pages
- 2361-2369
- ISSN
- 0197-4580 (ISSN-L)
- PMC
- PMC3706498
- OpenAlex
- W1995510295
- Cited by
- 32
- References
- 57
- Citations by year
- 2025: 3 · 2024: 3 · 2022: 3 · 2021: 6 · 2020: 3 · 2019: 3 · 2018: 2 · 2017: 1 · 2016: 1 · 2015: 5 · 2014: 2
- FWCI
- 1.85
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Neurobiology of Aging (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Department of Veterans Affairs (VA 247-P-0447, VA 240-12-C-0051)
- NIH (RR019963, OD010965, RO1-HL87103)
- Roena Kulynych Center for Memory and Cognition Research
- Claude D. Pepper Older Americans Independence Center of Wake Forest School of Medicine (P30-AG21332)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- amyloid burden, vervet monkey, Alzheimer's disease model, amyloid-beta 42, amyloid plaques, norepinephrine, astrocyte activation, glial fibrillary acidic protein, glial cell line-derived neurotrophic factor, aging, posterior temporal lobe, nonhuman primate model
- MeSH terms
- Aging, Alzheimer Disease, Animals, Astrocytes, Chlorocebus aethiops, Cerebral Cortex, Disease Models, Animal, Female, Glial Fibrillary Acidic Protein, Norepinephrine, Peptide Fragments, Temporal Lobe, Amyloid beta-Peptides, Brain-Derived Neurotrophic Factor, Plaque, Amyloid
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