1. Quercetin protects against perfluorooctanoic acid-induced liver injury by attenuating oxidative stress and inflammatory response in mice
- Author
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Lei Wu, Wenwen Liu, Ting Zou, Weiying Zou, Fangming Liu, Liping Xia, Bei Yang, Jianhua Yang, and Dalei Zhang
- Subjects
Male ,medicine.medical_specialty ,Immunology ,Apoptosis ,Inflammation ,medicine.disease_cause ,Antioxidants ,Proinflammatory cytokine ,Bile Acids and Salts ,Mice ,chemistry.chemical_compound ,Liver Function Tests ,Internal medicine ,Lactate dehydrogenase ,medicine ,Animals ,Immunology and Allergy ,Pharmacology ,Liver injury ,Fluorocarbons ,Chemistry ,Anti-Inflammatory Agents, Non-Steroidal ,medicine.disease ,Malondialdehyde ,Oxidative Stress ,Endocrinology ,Hepatocytes ,Cytokines ,Alkaline phosphatase ,Quercetin ,Liver function ,Caprylates ,Chemical and Drug Induced Liver Injury ,medicine.symptom ,Oxidative stress - Abstract
The aim of the present study was to investigate the protective effect of quercetin (Que) against perfluorooctanoic acid (PFOA)-induced liver injury in mice and its possible mechanisms of action. Mice were intragastrically administered PFOA (10mg/kg/day) alone or in combination with Que (75 mg/kg/day) for 14 consecutive days. The hepatic injury was evaluated by measuring morphological changes, liver function, oxidative stress, inflammatory response and hepatocellular apoptosis. Compared with mice treated with PFOA alone, simultaneous supplementation of Que significantly decreased serum levels of liver injury indicators alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, lactate dehydrogenase and total bile acids. Moreover, Que treatment inhibited the production of oxidative stress biomarkers malondialdehyde, hydrogen peroxide and 8-hydroxy-2'-deoxyguanosine, reduced the levels of proinflammatory cytokines interleukin 6, cyclooxygenase-2 and C-reactive protein, and decreased the number of TUNEL-positive cells in the liver of PFOA-treated mice. These results combined with liver histopathology demonstrated that Que exhibited a potential protective effect against PFOA-induced liver damage via mechanisms involving the attenuation of oxidative stress, alleviation of inflammation and inhibition of hepatocellular apoptosis.
- Published
- 2015