Cited by 340Genetics, Aging, and Longevity in Model OrganismsDietary Effects on HealthSirtuins and Resveratrol in Medicine

Dietary restriction and lifespan: lessons from invertebrate models

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Kapahi, Pankaj, Kaeberlein, Matt, Hansen, Malene·2017·Ageing Research Reviews

Abstract

Dietary restriction (DR) is the most robust environmental manipulation known to increase active and healthy lifespan in many species. Despite differences in the protocols and the way DR is carried out in different organisms, conserved relationships are emerging among multiple species. Elegant studies from numerous model organisms are further defining the importance of various nutrient-signaling pathways including mTOR (mechanistic target of rapamycin), insulin/IGF-1-like signaling and sirtuins in mediating the effects of DR. We here review current advances in our understanding of the molecular mechanisms altered by DR to promote lifespan in three major invertebrate models, the budding yeast Saccharomyces cerevisiae, the nematode Caenorhabditis elegans, and the fruit fly Drosophila melanogaster.

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  • Signal modulations including mRNA translation, transcription, autophagy, and mitochondrial function have been shown to mediate extended lifespan.

    “These signal modulations, including mRNA translation, transcription, autophagy, and mitochondrial function, have been shown to mediate extended lifespan [186].”

    From Immunosenescence: a key player in cancer development (2020) · cites this paper as [186]

  • The round worm Caenorhabditis elegans is used to investigate metabolic pathways and has been instrumental in elucidating key genetic regulators of metabolism in relation to lifespan.

    “The round worm Caenorhabditis elegans, for instance, is used to investigate metabolic pathways and has been instrumental in elucidating key genetic regulators of metabolism in relation to lifespan (36, 293, 294).”
  • Dietary restrictions increase lifespan and healthspan in all animal models of aging (yeast, C. elegans, Drosophila, mouse).

    “Dietary restrictions have been shown to increase lifespan and healthspan in all animal models of aging (e.g., yeast, C. elegans, Drosophila, mouse) [239,289,290,291].”
  • Nutrient-sensing mTOR and insulin/IGF1 pathways mediate the effect of dietary restriction on aging.

    “It is evident that the nutrient-sensing mTOR and the insulin/IGF1 pathways mediate the effect of dietary restriction on aging [149,291].”

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References 187 · Cited by 340

Authors
Kapahi, P., Kaeberlein, M., & Hansen, M.
Affiliations
  • Buck Institute for Research on Aging (US)
  • University of Washington (US)
  • Sanford Burnham Prebys Medical Discovery Institute (US)
Corresponding author
Hansen, Malene
Venue
Ageing Research Reviews
Publisher
Elsevier BV
Published
2017-10
Volume
39
Pages
3-14
ISSN
1568-1637 (ISSN-L)
OpenAlex
W2564232696
Cited by
340
References
187
Citations by year
2026: 17 · 2025: 26 · 2024: 33 · 2023: 40 · 2022: 44 · 2021: 62 · 2020: 38 · 2019: 39 · 2018: 27 · 2017: 13
FWCI
2.64
Type
journal article
Language
en
Open access
Locations
  • Ageing Research Reviews (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • NIH (R01AG038688, AG045835, AG038518, AG031108, AG005136, AG013280, AG038664, AG039756)
  • AFAR
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Health Sciences › Medicine › Physiology › Dietary Effects on Health
  • Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
Keywords
dietary restriction, lifespan extension, invertebrate models, mTOR, insulin/IGF-1 signaling, sirtuins, Saccharomyces cerevisiae, Caenorhabditis elegans, Drosophila melanogaster, aging
MeSH terms
Animals, Drosophila, Drosophila melanogaster, Insulin, Insulin-Like Growth Factor I, Longevity, Recombinant Proteins, Saccharomyces cerevisiae, Signal Transduction, Caenorhabditis elegans, Models, Animal, Caloric Restriction, Sirtuins, TOR Serine-Threonine Kinases

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