Volume 53, Issue 1 p. 147-155
Original Article

Antioxidant activity of blueberry anthocyanin extracts and their protective effects against acrylamide-induced toxicity in HepG2 cells

Xuenan Li

Xuenan Li

College of Food Science and Engineering, Jilin University, Changchun, 130062 China

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Huangyou Liu

Huangyou Liu

College of Food Science and Engineering, Jilin University, Changchun, 130062 China

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Lingzhu Lv

Lingzhu Lv

College of Food Science and Engineering, Jilin University, Changchun, 130062 China

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Haiyang Yan

Haiyang Yan

College of Food Science and Engineering, Jilin University, Changchun, 130062 China

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Yuan Yuan

Corresponding Author

Yuan Yuan

College of Food Science and Engineering, Jilin University, Changchun, 130062 China

Correspondent: E-mail: [email protected]Search for more papers by this author
First published: 23 November 2017
Citations: 28
Xuenan Li and Huangyou Liu are the joint first author.

Summary

In this study, the antioxidant activities of blueberry anthocyanin extracts from ten blueberry varieties were evaluated based on the methods of scavenging activities for DPPH radicals, ABTS radicals, hydroxyl radicals and ferric reducing antioxidant power (FRAP) assay. Among the ten blueberry varieties, Polaris had the highest antioxidant abilities and the largest amounts of anthocyanins identified by HPLC-MS. The protective effects of anthocyanin extracts from Polaris (AEP) against acrylamide (AA)-induced toxicity in HepG2 cell models were also evaluated due to the neurotoxic, genotoxic and potentially carcinogenic effects of AA. The protective effects of AEP on the damage of HepG2 cells were explored from the aspects of cell viability, T-SOD and CAT activity and MDA level. The AEP (5, 10, 20 μg mL−1) could significantly increase cell viability (< 0.01) and inhibit AA-induced cytotoxicity. Polaris also markedly promoted the activity of SOD, CAT and inhibited MDA level. The results showed that AEP had strong antioxidant activities, presenting high protective effects against AA-induced cell damage in HepG2 cell models.