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Monascin from Monascus-Fermented Products Reduces Oxidative Stress and Amyloid-β Toxicity via DAF-16/FOXO in Caenorhabditis elegans
被引:39
|作者:
Shi, Yeu-Ching
[1
]
Pan, Tzu-Ming
[2
]
Liao, Vivian Hsiu-Chuan
[1
]
机构:
[1] Natl Taiwan Univ, Dept Bioenvironm Syst Engn, 1,Sec 4,Roosevelt Rd, Taipei 106, Taiwan
[2] Natl Taiwan Univ, Dept Biochem Sci & Technol, 1,Sec 4,Roosevelt Rd, Taipei 106, Taiwan
关键词:
Alzheimer's disease (AD);
amyloid-beta;
monascin;
fungus secondary metabolite;
Caenorhabditis elegans;
oxidative stress;
DAF-16;
ALZHEIMERS-DISEASE;
PEROXIREDOXIN-II;
MONACOLIN K;
PPAR-GAMMA;
C-ELEGANS;
LIFE-SPAN;
MODEL;
HYPERGLYCEMIA;
EXPRESSION;
PEPTIDE;
D O I:
10.1021/acs.jafc.6b02779
中图分类号:
S [农业科学];
学科分类号:
09 ;
摘要:
Amyloid-beta-(A beta)-induced oxidative-stress and toxicity are leading risk factors. for Alzheimer's disease (AD). Monascin (MS) is a novel compound proposed for antioxidative stress applications and is derived from an edible fungus secondary metabolite. This study assessed the effects of MS on oxidative stress, paralysis, A beta accumulation, and lifespan in the nematode Caenorhabditis elegans and investigated its underlying mechanisms of action. The results showed that MS increased the survival of C. elegans under juglone-induced oxidative stress and attenuated endogenous levels,of reactive oxygen species. Furthermore, MS induced a decline in A beta-induced paralysis phenotype and A beta deposits in the transgenic strains CL4176 and CL2006 of C. elegans, which expresses human muscle-specific A beta(1-42) in the cytoplasm of body wall muscle cells. In addition, mRNA levels of strain CI4176 of several antioxidant genes (sod-1, sod-2, sod-3, hsp16.2) and daf-16 were up-regulated by MS treatment when compared to the nontreated controls. Further evidence showed that MS treatment in C. elegans strains lacking DAF-16/FOXO did not affect paralysis or lifespan phenotypes. The findings indicate that MS reduces oxidative stress and A beta toxicity via DAF-16 in C. elegans, suggesting that MS can be used for the prevention of AD-associated oxidative stress complications.
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页码:7114 / 7120
页数:7
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