Dr. Daniele Bano
German Center for Neurodegenerative Diseases (DZNE)
daniele.bano@dzne.de View member: Dr. Daniele Bano
Nature communications
Current concepts regarding the biology of aging are primarily based on studies aimed at identifying factors regulating lifespan. However, lifespan as a sole proxy measure for aging can be of limited value because it may be restricted by specific pathologies. Here, we employ large-scale phenotyping to analyze hundreds of markers in aging male C57BL/6J mice. For each phenotype, we establish lifetime profiles to determine when age-dependent change is first detectable relative to the young adult baseline. We examine key lifespan regulators (putative anti-aging interventions; PAAIs) for a possible countering of aging. Importantly, unlike most previous studies, we include in our study design young treated groups of animals, subjected to PAAIs prior to the onset of detectable age-dependent phenotypic change. Many PAAI effects influence phenotypes long before the onset of detectable age-dependent change, but, importantly, do not alter the rate of phenotypic change. Hence, these PAAIs have limited effects on aging.
© 2022. The Author(s).
PMID: 36369285
German Center for Neurodegenerative Diseases (DZNE)
daniele.bano@dzne.de View member: Dr. Daniele BanoGerman Center for Neurodegenerative Diseases (DZNE)
monique.breteler@dzne.de View member: Prof. Dr. Monique Breteler