TY - JOUR
T1 - A New Preclinical Paradigm for Testing Anti-Aging Therapeutics
AU - Ladiges, Warren
AU - Snyder, Jessica M.
AU - Wilkinson, Erby
AU - Imai, Denise M.
AU - Snider, Tim
AU - Ge, Xuan
AU - Ciol, Marcia
AU - Pettan-Brewer, Christina
AU - Pillai, Smitha P.S.
AU - Morton, John
AU - Quarles, Ellen
AU - Rabinovitch, Peter
AU - Niedernhofer, Laura
AU - Liggitt, Denny
N1 - Publisher Copyright:
© The Author 2017
PY - 2017/6/1
Y1 - 2017/6/1
N2 - 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.
AB - 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.
KW - Aging
KW - Aging lesions in mice
KW - Anti-aging therapeutics
KW - Geropathology Grading Platform
KW - Preclinical drug testing
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U2 - 10.1093/gerona/glx019
DO - 10.1093/gerona/glx019
M3 - Article
C2 - 28329081
AN - SCOPUS:85027489098
SN - 1079-5006
VL - 72
SP - 760
EP - 762
JO - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
JF - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
IS - 6
ER -