| Literature DB >> 29353102 |
Paige E Cramer1, Renee C Gentzel1, Keith Q Tanis2, Joshua Vardigan3, Yi Wang1, Brett Connolly4, Philip Manfre5, Kenneth Lodge6, John J Renger1, Celina Zerbinatti1, Jason M Uslaner7.
Abstract
While many preclinical models of Alzheimer's disease (AD) have been reported, none fully recapitulate the disease. In an effort to identify an appropriate preclinical disease model, we characterized age-related changes in 2 higher order species, the African green monkey (AGM) and the rhesus macaque. Gene expression profiles in the dorsolateral prefrontal cortex and the visual cortex showed age-related changes in AGMs that are strikingly reminiscent of AD, whereas aged rhesus were most similar to healthy elderly humans. Biochemically, age-related changes in AGM cerebrospinal fluid levels of tau, phospho-tau, and amyloid beta were consistent with AD. Histologically, aged AGMs displayed pathological hallmarks of the disease, plaques, and 2 AGMs showed evidence of neurofibrillary tangle-like structures. We hypothesized and confirmed that AGMs have age-related cognitive deficits via a prefrontal cortex-dependent cognition test, and that symptomatic treatments that improve cognition in AD patients show efficacy in AGMs. These data suggest that the AGM could represent a novel and improved translational model to assist in the development of therapeutics for AD.Entities:
Keywords: African green monkey; Alzheimer's disease; Amyloid beta; Cognition; Rhesus; Tau
Mesh:
Substances:
Year: 2017 PMID: 29353102 DOI: 10.1016/j.neurobiolaging.2017.12.011
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673