The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα Activation
Objective. Previous studies have characterized the hepatoprotective and anti-inflammatory properties of oleanolic acid (OA). This study aimed to investigate the molecular mechanisms of OA hepatoprotection in concanavalin A- (ConA-) induced acute liver injury. Materials and Methods. ConA (20 mg/kg) w...
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Online Access: | http://dx.doi.org/10.1155/2018/3180396 |
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doaj-81e8a196b16e4fc499001bbc858273662020-11-24T22:30:25ZengHindawi LimitedPPAR Research1687-47571687-47652018-01-01201810.1155/2018/31803963180396The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα ActivationWenwen Wang0Kan Chen1Yujing Xia2Wenhui Mo3Fan Wang4Weiqi Dai5Peiqin Niu6Department of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaDepartment of Gastroenterology, Minhang Hospital, Fudan University, Shanghai 201100, ChinaDepartment of Oncology, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200080, ChinaDepartment of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai 200032, ChinaDepartment of Gastroenterology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai 200072, ChinaObjective. Previous studies have characterized the hepatoprotective and anti-inflammatory properties of oleanolic acid (OA). This study aimed to investigate the molecular mechanisms of OA hepatoprotection in concanavalin A- (ConA-) induced acute liver injury. Materials and Methods. ConA (20 mg/kg) was intravenously injected to induce acute liver injury in Balb/C mice. OA pretreatment (20, 40, and 80 mg/kg) was administered subcutaneously once daily for 3 consecutive days prior to treatment with ConA; 2, 8, and 24 h after ConA injection, the levels of serum liver enzymes and the histopathology of major factors and inflammatory cytokines were determined. Results. OA reduced the release of serum liver enzymes and inflammatory factors and prevented ConA mediated damage to the liver. OA elevated the expression levels of peroxisome proliferator-activated receptor alpha (PPARα) and decreased the phosphorylation of c-Jun NH2-terminal kinase (JNK). Conclusion. OA exhibits anti-inflammatory properties during ConA-induced acute liver injury by attenuating apoptosis and autophagy through activation of PPARα and downregulation of JNK signaling.http://dx.doi.org/10.1155/2018/3180396 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wenwen Wang Kan Chen Yujing Xia Wenhui Mo Fan Wang Weiqi Dai Peiqin Niu |
spellingShingle |
Wenwen Wang Kan Chen Yujing Xia Wenhui Mo Fan Wang Weiqi Dai Peiqin Niu The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα Activation PPAR Research |
author_facet |
Wenwen Wang Kan Chen Yujing Xia Wenhui Mo Fan Wang Weiqi Dai Peiqin Niu |
author_sort |
Wenwen Wang |
title |
The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα Activation |
title_short |
The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα Activation |
title_full |
The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα Activation |
title_fullStr |
The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα Activation |
title_full_unstemmed |
The Hepatoprotection by Oleanolic Acid Preconditioning: Focusing on PPARα Activation |
title_sort |
hepatoprotection by oleanolic acid preconditioning: focusing on pparα activation |
publisher |
Hindawi Limited |
series |
PPAR Research |
issn |
1687-4757 1687-4765 |
publishDate |
2018-01-01 |
description |
Objective. Previous studies have characterized the hepatoprotective and anti-inflammatory properties of oleanolic acid (OA). This study aimed to investigate the molecular mechanisms of OA hepatoprotection in concanavalin A- (ConA-) induced acute liver injury. Materials and Methods. ConA (20 mg/kg) was intravenously injected to induce acute liver injury in Balb/C mice. OA pretreatment (20, 40, and 80 mg/kg) was administered subcutaneously once daily for 3 consecutive days prior to treatment with ConA; 2, 8, and 24 h after ConA injection, the levels of serum liver enzymes and the histopathology of major factors and inflammatory cytokines were determined. Results. OA reduced the release of serum liver enzymes and inflammatory factors and prevented ConA mediated damage to the liver. OA elevated the expression levels of peroxisome proliferator-activated receptor alpha (PPARα) and decreased the phosphorylation of c-Jun NH2-terminal kinase (JNK). Conclusion. OA exhibits anti-inflammatory properties during ConA-induced acute liver injury by attenuating apoptosis and autophagy through activation of PPARα and downregulation of JNK signaling. |
url |
http://dx.doi.org/10.1155/2018/3180396 |
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