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Oxid Med Cell Longev. 2017;2017:7956158. doi: 10.1155/2017/7956158. Epub 2017 Jun 21.

Mulberry Anthocyanin Extract Ameliorates Oxidative Damage in HepG2 Cells and Prolongs the Lifespan of Caenorhabditis elegans through MAPK and Nrf2 Pathways.

Yan F1,2,3, Chen Y1,2,3, Azat R1,2,3, Zheng X1,2,3.

Author information

1
Department of Food Science and Nutrition, Zhejiang University, Hangzhou 310058, China.
2
Zhejiang Key Laboratory for Agro-food Processing, Zhejiang University, Hangzhou 310058, China.
3
Fuli Institute of Food Science, Zhejiang University, Hangzhou 310058, China.

Abstract

Mulberry anthocyanins possess many pharmacological effects including liver protection, anti-inflammation, and anticancer. The aim of this study was to evaluate whether mulberry anthocyanin extract (MAE) exerts beneficial effects against oxidative stress damage in HepG2 cells and Caenorhabditis elegans. In vitro, MAE prevented cytotoxicity, increased glucose consumption and uptake, and eliminated excessive intracellular free radicals in H2O2-induced cells. Moreover, MAE pretreatment maintained Nrf2, HO-1, and p38 MAPK stimulation and abolished upregulation of p-JNK, FOXO1, and PGC-1α that were involved in oxidative stress and insulin signalling modulation. In vivo, extended lifespan was observed in C. elegans damaged by paraquat in the presence of MAE, while these beneficial effects were disappeared in pmk-1 and daf-16 mutants. PMK-1 and SKN-1 were activated after exposure to paraquat and MAE suppressed PMK-1 activation but enhanced SKN-1 stimulation. Our findings suggested that MAE recovered redox status in HepG2 cells and C. elegans that suffered from oxidative stress, which might be by targeting MAPKs and Nrf2.

PMID:
28713491
PMCID:
PMC5497675
DOI:
10.1155/2017/7956158
[Indexed for MEDLINE]
Free PMC Article

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