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Research Paper|Volume 16, Issue 7|pp 5829—5855

The coupling between healthspan and lifespan in Caenorhabditis depends on complex interactions between compound intervention and genetic background

Stephen A. Banse1, E. Grace Jackson1, Christine A. Sedore1, Brian Onken2, David Hall3, Anna Coleman-Hulbert1, Phu Huynh2, Theo Garrett3, Erik Johnson1, Girish Harinath2, Delaney Inman3, Suzhen Guo2, Mackenzie Morshead3, Jian Xue2, Ron Falkowski2, Esteban Chen2, Christopher Herrera2, Allie J. Kirsch1, Viviana I. Perez4, Max Guo4, Gordon J. Lithgow3, Monica Driscoll2, Patrick C. Phillips1
  • 1Institute of Ecology and Evolution, University of Oregon, Eugene, OR 97403, USA
  • 2Department of Molecular Biology and Biochemistry, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA
  • 3The Buck Institute for Research on Aging, Novato, CA 94945, USA
  • 4Division of Aging Biology, National Institute on Aging, Bethesda, MD 20892, USA
* Equal contribution
Received: September 19, 2023Accepted: January 11, 2024Published: April 12, 2024

Copyright: © 2024 Banse et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Aging is characterized by declining health that results in decreased cellular resilience and neuromuscular function. The relationship between lifespan and health, and the influence of genetic background on that relationship, has important implications in the development of pharmacological anti-aging interventions. Here we assessed swimming performance as well as survival under thermal and oxidative stress across a nematode genetic diversity test panel to evaluate health effects for three compounds previously studied in the Caenorhabditis Intervention Testing Program and thought to promote longevity in different ways – NP1 (nitrophenyl piperazine-containing compound 1), propyl gallate, and resveratrol. Overall, we find the relationships among median lifespan, oxidative stress resistance, thermotolerance, and mobility vigor to be complex. We show that oxidative stress resistance and thermotolerance vary with compound intervention, genetic background, and age. The effects of tested compounds on swimming locomotion, in contrast, are largely species-specific. In this study, thermotolerance, but not oxidative stress or swimming ability, correlates with lifespan. Notably, some compounds exert strong impact on some health measures without an equally strong impact on lifespan. Our results demonstrate the importance of assessing health and lifespan across genetic backgrounds in the effort to identify reproducible anti-aging interventions, with data underscoring how personalized treatments might be required to optimize health benefits.