4.5 Article

Antistress and anti-aging activities ofCaenorhabditis eleganswere enhanced byMomordicasaponin extract

Journal

EUROPEAN JOURNAL OF NUTRITION
Volume 60, Issue 4, Pages 1819-1832

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00394-020-02338-6

Keywords

Momordicasaponins extract; Caenorhabditis elegans; Antistress; Anti-aging; Antioxidant activity

Funding

  1. National Natural Science Foundation of China [31700501]
  2. Science and Technology Planning Project of Guangdong Province, China [2017A020208042]
  3. National Key RD Program [2016YFD0600806]

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Momordica saponin extract (MSE) not only improves longevity and neuroprotection, but also alleviates fat accumulation inCaenorhabditis elegans. MSE shows strong antioxidant activities by increasing SOD and CAT activities, reducing ROS and lipid oxidation. Furthermore, MSE upregulates the expression of stress resistance genes and induces nuclear DAF-16::GFP localization, suggesting its potential as a nutraceutical in geriatric research.
Background Momordica saponin extract (MSE) was found to not only improve longevity and neuroprotection but also alleviate fat accumulation inCaenorhabditis elegansin our previous study. However, the lipid-lowering activity of MSE alone could not fully explain its ability to improve health, so the antistress effects of MSE were further studied. Methods UsingC. elegansas an in vivo animal, the lifespan of MSE-treatedC. elegansunder various stressors (H2O2, paraquat and heat) and normal conditions was studied. Furthermore, the antioxidant activities of MSE were discussed. To study the underlying mechanisms, the expression of stress resistance genes and the resistance of related mutants to H(2)O(2)stress were tested. Results MSE significantly improved the lifespan ofC. elegansunder stress and normal conditions. Meanwhile, the mobility ofC. eleganswas also improved. Moreover, the activities of SOD and CAT and the ratio of GSH/GSSG were elevated. Consistently, the levels of ROS and lipid oxidation (the NEFA and MDA content) were reduced. Furthermore, MSE treatment upregulated the expression of thesod-3,sod-5,clt-1,clt-2,hsp-16.1andhsp-16.2genes. All biomarkers indicated that the antistress and anti-aging activities of MSE were due to its strong antioxidant activities. Finally, MSE induced nuclear DAF-16::GFP localization. Studies with mutants revealed thatskn-1andhsf-1were involved in the activity of MSE, which might upregulate the expression of downstream stress-responsive genes. Conclusions Therefore, in addition to its lipid-lowering property, the ability of MSE to improve healthspan was also attributed to the stress resistance effect. Together, MSE might serve as a lead nutraceutical in geriatric research.

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