TY - JOUR
T1 - Energetic interventions for healthspan and resiliency with aging
AU - Huffman, Derek M.
AU - Schafer, Marissa J.
AU - LeBrasseur, Nathan K.
N1 - Funding Information:
This work was supported by the Glenn Foundation for Medical Research (NKL and MJS) and NIH /NIA grant AG041122 (NKL). D.M.H is supported by NIA R00AG037574 , P30AG038072 , the Einstein-Sinai Diabetes Research Center ( P30DK20541 ) and the American Federation for Aging Research (AFAR).
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/12/15
Y1 - 2016/12/15
N2 - Several behavioral and pharmacological strategies improve longevity, which is indicative of delayed organismal aging, with the most effective interventions extending both life- and healthspan. In free living creatures, maintaining health and function into old age requires resilience against a multitude of stressors. Conversely, in experimental settings, conventional housing of rodents limits exposure to such challenges, thereby obscuring an accurate assessment of resilience. Caloric restriction (CR) and exercise, as well as pharmacologic strategies (resveratrol, rapamycin, metformin, senolytics), are well established to improve indices of health and aging, but some paradoxical effects have been observed on resilience. For instance, CR potently retards the onset of age-related diseases, and improves lifespan to a greater extent than exercise in a variety of models. However, exercise has proven more consistently beneficial to organismal resilience against a broad array of stressors, including infections, surgery, wound healing and frailty. CR can improve cellular stress defenses and protect from frailty, but also impairs the response to infections, bed rest and healing. How an intervention will impact not only longevity, health and function, but also resiliency, is critical to better understanding translational implications. Thus, organismal robustness represents a critical, albeit understudied aspect of aging, which needs more careful attention in order to better inform on how putative age-delaying strategies will impact preservation of health and function in response to stressors with aging in humans.
AB - Several behavioral and pharmacological strategies improve longevity, which is indicative of delayed organismal aging, with the most effective interventions extending both life- and healthspan. In free living creatures, maintaining health and function into old age requires resilience against a multitude of stressors. Conversely, in experimental settings, conventional housing of rodents limits exposure to such challenges, thereby obscuring an accurate assessment of resilience. Caloric restriction (CR) and exercise, as well as pharmacologic strategies (resveratrol, rapamycin, metformin, senolytics), are well established to improve indices of health and aging, but some paradoxical effects have been observed on resilience. For instance, CR potently retards the onset of age-related diseases, and improves lifespan to a greater extent than exercise in a variety of models. However, exercise has proven more consistently beneficial to organismal resilience against a broad array of stressors, including infections, surgery, wound healing and frailty. CR can improve cellular stress defenses and protect from frailty, but also impairs the response to infections, bed rest and healing. How an intervention will impact not only longevity, health and function, but also resiliency, is critical to better understanding translational implications. Thus, organismal robustness represents a critical, albeit understudied aspect of aging, which needs more careful attention in order to better inform on how putative age-delaying strategies will impact preservation of health and function in response to stressors with aging in humans.
KW - Aging
KW - Caloric restriction
KW - Diet
KW - Exercise
KW - Metformin
KW - Rapamycin
KW - Resiliency
KW - Resveratrol
KW - Robustness
KW - Senolytics
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U2 - 10.1016/j.exger.2016.05.012
DO - 10.1016/j.exger.2016.05.012
M3 - Article
C2 - 27260561
AN - SCOPUS:85002293044
SN - 0531-5565
VL - 86
SP - 73
EP - 83
JO - Experimental Gerontology
JF - Experimental Gerontology
ER -