| Literature DB >> 28329081 |
Warren Ladiges1,2, Jessica M Snyder1, Erby Wilkinson3, Denise M Imai4, Tim Snider5, Xuan Ge1, Marcia Ciol6, Christina Pettan-Brewer1, Smitha P S Pillai7, John Morton1, Ellen Quarles2, Peter Rabinovitch2, Laura Niedernhofer8, Denny Liggitt1.
Abstract
Testing drugs for anti-aging effects has historically been conducted in mouse life-span studies, but are costly and time consuming, and more importantly, difficult to recapitulate in humans. In addition, life-span studies in mice are not well suited to testing drug combinations that target multiple factors involved in aging. Additional paradigms for testing therapeutics aimed at slowing aging are needed. A new paradigm, designated as the Geropathology Grading Platform (GGP), is based on a standardized set of guidelines developed to detect the presence or absence of low-impact histopathological lesions and to determine the level of severity of high-impact lesions in organs from aged mice. The GGP generates a numerical score for each age-related lesion in an organ, summed for total lesions, and averaged over multiple mice to obtain a composite lesion score (CLS). Preliminary studies show that the platform generates CLSs that increase with the age of mice in an organ-dependent manner. The CLSs are sensitive enough to detect changes elicited by interventions that extend mouse life span, and thus help validate the GGP as a novel tool to measure biological aging. While currently optimized for mice, the GGP could be adapted to any preclinical animal model.Entities:
Keywords: Aging; Aging lesions in mice; Anti-aging therapeutics; Geropathology Grading Platform; Preclinical drug testing
Mesh:
Year: 2017 PMID: 28329081 PMCID: PMC6075196 DOI: 10.1093/gerona/glx019
Source DB: PubMed Journal: J Gerontol A Biol Sci Med Sci ISSN: 1079-5006 Impact factor: 6.053