共 50 条
Green tea polyphenols and epigallocatechin-3-gallate protect against perfluorodecanoic acid induced liver damage and inflammation in mice by inhibiting NLRP3 inflammasome activation
被引:0
|作者:
Wang, Dongxu
[1
]
Gao, Qiang
[1
]
Wang, Taotao
[2
]
Kan, Zhipeng
[1
]
Li, Xin
[1
]
Hu, Lizhen
[1
]
Peng, Chuan-yi
[1
]
Qian, Frank
[3
]
Wang, Yijun
[1
]
Granato, Daniel
[4
]
机构:
[1] State Key Laboratory of Tea Plant Biology and Utilization, School of Tea and Food Science & Technology, Anhui Agricultural University, Hefei,Anhui,230036, China
[2] Department of Clinical Nutrition, Affiliated Hospital of Jiangsu University, Zhenjiang,Jiangsu,212000, China
[3] Pritzker School of Medicine, University of Chicago, Chicago,IL,60637, United States
[4] Food Processing and Quality, Production Systems Unit, Natural Resources Institute Finland, Luke, Maarintie 6, Open Innovation House, Espoo,FI-02150, Finland
关键词:
Pathology - Chemical contamination - Cell death - Chemical activation - Mammals;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Perfluorodecanoic acid (PFDA) is a highly toxic food contaminant that is extensively used in food applications as surface antifouling agent. In this present study, we aimed to assess whether green tea polyphenols (GTPs) and epigallocatechin-3-gallate (EGCG) exert protective effects against PFDA-induced liver damage and inflammation in mice. A mouse model to evaluate liver toxicity was established by giving mice drinking water containing different concentrations of PFDA. GTPs or EGCG (0.32%, w/v) were co-administered to mice exposed to PFDA in drinking water. Overall, GTPs and EGCG extended the survival time and inhibited weight loss among mice who received a lower dose of PFDA. Moreover, GTPs and EGCG ameliorated hepatic oxidative stress, cell apoptosis, necrosis, steatosis, edema, and degeneration, reduced hepatic inflammation and NLRP3 inflammasome activation caused by a moderate dose of PFDA. Taken together, these results show that GTPs or EGCG (or green tea intake) supplements can be beneficial for people exposed to PFDA. © 2019 Elsevier Ltd
引用
收藏
相关论文