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Monascus-Fermented Dioscorea Enhances Oxidative Stress Resistance via DAF-16/FOXO in Caenorhabditis elegans
被引:26
作者:
Shi, Yeu-Ching
[1
]
Yu, Chan-Wei
[1
]
Liao, Vivian Hsiu-Chuan
[1
]
Pan, Tzu-Ming
[2
]
机构:
[1] Natl Taiwan Univ, Dept Bioenvironm Syst Engn, Taipei 10764, Taiwan
[2] Natl Taiwan Univ, Dept Biochem Sci & Technol, Taipei 10764, Taiwan
来源:
PLOS ONE
|
2012年
/
7卷
/
06期
关键词:
INDUCED DIABETIC-RATS;
RED MOLD DIOSCOREA;
PURPUREUS NTU 568;
LIFE-SPAN;
SUPEROXIDE DISMUTASES;
HYDROGEN-PEROXIDE;
MODEL ORGANISM;
CANCER-CELLS;
C-ELEGANS;
DISEASE;
D O I:
10.1371/journal.pone.0039515
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Background: Monascus-fermented products are mentioned in an ancient Chinese pharmacopoeia of medicinal food and herbs. Monascus-fermented products offer valuable therapeutic benefits and have been extensively used in East Asia for several centuries. Several biological activities of Monascus-fermented products were recently described, and the extract of Monascus-fermented products showed strong antioxidant activity of scavenging DPPH radicals. To evaluate whether Monascus-fermented dioscorea products have potential as nutritional supplements, Monascus-fermented dioscorea's modulation of oxidative-stress resistance and associated regulatory mechanisms in Caenorhabditis elegans were investigated. Principal Findings: We examined oxidative stress resistance of the ethanol extract of red mold dioscorea (RMDE) in C. elegans, and found that RMDE-treated wild-type C. elegans showed an increased survival during juglone-induced oxidative stress compared to untreated controls, whereas the antioxidant phenotype was absent from a daf-16 mutant. In addition, the RMDE reduced the level of intracellular reactive oxygen species in C. elegans. Finally, the RMDE affected the subcellular distribution of the FOXO transcription factor, DAF-16, in C. elegans and induced the expression of the sod-3 antioxidative gene. Conclusions: These findings suggest that the RMDE acts as an antioxidative stress agent and thus may have potential as a nutritional supplement. Further studies in C. elegans suggest that the antioxidant effect of RMDE is mediated via regulation of the DAF-16/FOXO-dependent pathway.
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