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Phytoecdysteroid-enriched quinoa seed leachate enhances healthspan and mitochondrial metabolism in Caenorhabditis elegans

•Quinoa enhanced C. elegans median lifespan, locomotory vigor, and mitochondrial respiration.•Quinoa reduced AGE pigment, reactive oxygen species, and fat accumulation in C. elegans.•20-hydroxyecdysone is a primary bioactive constituent of quinoa. Quinoa (Chenopodium quinoa Willd.) phytochemicals ha...

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Published in:Journal of functional foods 2017-10, Vol.37, p.1-7
Main Authors: Graf, Brittany L., Kamat, Shaunak, Cheong, Kuan Yu, Komarnytsky, Slavko, Driscoll, Monica, Di, Rong
Format: Article
Language:English
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Summary:•Quinoa enhanced C. elegans median lifespan, locomotory vigor, and mitochondrial respiration.•Quinoa reduced AGE pigment, reactive oxygen species, and fat accumulation in C. elegans.•20-hydroxyecdysone is a primary bioactive constituent of quinoa. Quinoa (Chenopodium quinoa Willd.) phytochemicals have exhibited metabolic benefit in mammals, though their effects on aging and mechanisms of action remain unknown. Caenorhabditis elegans offers a practical in vivo model to study bioactivity since major metabolic pathways are conserved across phyla. We explored the effects of phytoecdysteroid-enriched quinoa seed preparation, termed quinoa leachate (QL), on behavioral and biochemical endpoints of wild-type C. elegans health. QL treatment (1.0mg/mL or less) increased median lifespan from 9 to 11d, improved locomotory performance from 103.5 to 114.9 head thrashes/min, and enhanced basal respiration rate by 37%. QL also reduced advanced glycation end-product (AGE) pigments by 24%, reactive oxygen species (ROS) by 20%, and body fat by 14%. 20-Hydroxyecdysone (20HE), the primary phytoecdysteroid in QL, conferred statistically similar benefit compared to QL at equivalent doses. Data suggest that quinoa supplementation slows C. elegans aging and improves metabolic health, and 20HE is the primary bioactive constituent responsible for favorable effects.
ISSN:1756-4646
2214-9414
DOI:10.1016/j.jff.2017.07.016