4.7 Article

Tart Cherry Increases Lifespan inCaenorhabditis elegansby Altering Metabolic Signaling Pathways

Journal

NUTRIENTS
Volume 12, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/nu12051482

Keywords

C. elegans; tart cherry; lifespan; aging; oxidative stress; daf-16

Funding

  1. USDA NIFA AFRI Exploratory award [2014-07216]
  2. USDA NIFA AFRI award [2018-07980]
  3. NIH (NCCIH) [R15 AT 8879-01A1]
  4. NIH (NIA) [R15 AT 8879-01A1]
  5. NIH AWARD [RO1 AG051995-04]
  6. NASA [NNX15AL16G]
  7. NASA [807298, NNX15AL16G] Funding Source: Federal RePORTER

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Aging and healthspan are determined by both environmental and genetic factors. The insulin/insulin-like growth factor-1(IGF-1) pathway is a key mediator of aging inCaenorhabditis elegansand mammals. Specifically, DAF-2 signaling, an ortholog of human IGF, controls DAF-16/FOXO transcription factor, a master regulator of metabolism and longevity. Moreover, mitochondrial dysfunction and oxidative stress are both linked to aging. We propose that daily supplementation of tart cherry extract (TCE), rich in anthocyanins with antioxidant properties may exert dual benefits for mitochondrial function and oxidative stress, resulting in beneficial effects on aging inC. elegans. We found that TCE supplementation at 6 mu g or 12 mu g/mL, increased (p< 0.05) the mean lifespan of wild type N2 worms, respectively, when compared to untreated control worms. Consistent with these findings, TCE upregulated (p< 0.05) expression of longevity-related genes such asdaf-16andaak-2(but notdaf-2orakt-1genes) and genes related to oxidative stress such assod-2. Further, we showed that TCE supplementation increased spare respiration in N2 worms. However, TCE did not change the mean lifespan ofdaf-16andaak-2mutant worms. In conclusion, our findings indicate that TCE confers healthspan benefits inC. elegansthrough enhanced mitochondrial function and reduced oxidative stress, mainly via the DAF-16 pathway.

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