| Literature DB >> 33778327 |
Daniel S Evans1, Monique N O'Leary2, Ryan Murphy2, Minna Schmidt2, Kristin Koenig2, Michael Presley2, Brittany Garrett2, Ha-Neui Kim3, Li Han3, Emmeline C Academia2, Matt J Laye2, Daniel Edgar2, Christopher A Zambataro2, Tracey Barhydt2, Colleen M Dewey2, Jarrott Mayfield2, Joy Wilson2, Silvestre Alavez2, Mark Lucanic4, Brian K Kennedy2, Maria Almeida3, Julie K Andersen2, Pankaj Kapahi2, Gordon J Lithgow2, Simon Melov2.
Abstract
Aging is characterized by systemic declines in tissue and organ functions. Interventions that slow these declines represent promising therapeutics to protect against age-related disease and improve the quality of life. In this study, several interventions associated with lifespan extension in invertebrates or improvement of age-related disease were tested in mouse models to determine if they were effective in slowing tissue aging in a broad spectrum of functional assays. Benzoxazole, which extends the lifespan of Caenorhabditis elegans, slowed age-related femoral bone loss in mice. Rates of change were established for clinically significant parameters in untreated mice, including kyphosis, blood glucose, body composition, activity, metabolic measures, and detailed parameters of skeletal aging in bone. These findings have implications for the study of preclinical physiological aging and therapies targeting aging. Finally, an online application was created that includes the calculated rates of change and that enables power and variance to be calculated for many clinically important metrics of aging with an emphasis on bone. This resource will help in future study designs employing novel interventions in aging mice.Entities:
Keywords: AGING; BONE; MOLECULAR COMPUTED TOMOGRAPHY (mCT); OSTEOBLASTS; OSTEOCLASTS
Year: 2021 PMID: 33778327 PMCID: PMC7990142 DOI: 10.1002/jbm4.10466
Source DB: PubMed Journal: JBMR Plus ISSN: 2473-4039