Antagonism of Cyanamide-3-O-glucoside and protocatechuic acid on Aflatoxin B1-induced toxicity in zebrafish larva (Danio rerio)

被引:6
作者
Wu, Tian [1 ,2 ]
Fan, Tingting [1 ,2 ]
Xie, Yanli [1 ,2 ,3 ]
机构
[1] Henan Univ Technol, Coll Food Sci & Engn, Zhengzhou 450001, Peoples R China
[2] Henan Key Lab Cereal & Oil Food Safety Inspect & C, Zhengzhou 450001, Henan, Peoples R China
[3] Henan Univ Technol, Coll Food Sci & Engn, 100 Lianhua St,Hightech Ind Dev Zone, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
AflatoxinB(1); Cyanidin-3-O-glucoside; Protocatechuic acid; Zebrafish; Hepatotoxicity; Oxidative stress; OXIDATIVE STRESS; SEED COAT; ANTHOCYANINS; DETOXIFICATION; APOPTOSIS; ISOZYMES; EXPOSURE; PRODUCT; SYSTEMS; GROWTH;
D O I
10.1016/j.toxicon.2022.06.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The zebrafish model was used to evaluate the antioxidant properties of cyanidin-3-O-glucoside (C3G) and its metabolite protocatechuic acid (PCA) against aflatoxin B1 (AFB1)-induced hepatotoxicity and oxidative stress. In this study, zebrafish larvae were cultured for 3 days post fertilization (dpf) and then induced with AFB1. After induced 4 h, 8 h, 12 h, and 24 h, 5 mu g/mL C3G/PCA was added and then co-cultured to 5 dpf, respectively. The experiments showed that C3G/PCA suppressed AFB1-induced zebrafish liver atrophy and delayed the absorption of the yolk sac. In addition, reactive oxygen species (ROS) and cell death were also significantly decreased by 5 mu g/mL C3G/PCA (P < 0.05). C3G/PCA significantly reduced hepatic biomarkers in the serum contents (P < 0.05). Besides, glutathione (GSH) contents were significantly upregulated, and the activities of superoxide dismutase (SOD) and catalase (CAT) were significantly elevated in zebrafish (P < 0.05). The addition of 5 mu g/mL C3G/PCA was capable of reducing the apoptotic levels of caspase-9 and caspase-3 after 100 ng/mL AFB1 intoxication. In conclusion, these results suggested that C3G and its metabolite PCA might antagonize the hepatotoxicity of AFB1, reduce oxidative damage and inhibit cell death.
引用
收藏
页码:139 / 147
页数:9
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