PMID- 24933227 OWN - NLM STAT- MEDLINE DCOM- 20151022 LR - 20220408 IS - 1872-7573 (Electronic) IS - 0378-8741 (Linking) VI - 155 IP - 2 DP - 2014 Sep 11 TI - The mechanism of hepatoprotective effect of sesquiterpene rich fraction from Cichorum glandulosum Boiss. et Huet on immune reaction-induced liver injury in mice. PG - 1068-75 LID - S0378-8741(14)00462-0 [pii] LID - 10.1016/j.jep.2014.06.014 [doi] AB - ETHNOPHARMACOLOGICAL RELEVANCE: Cichorum glandulosum Boiss. et Huet is a traditional Uygur herbal medicine that has been used as a cholagogic and diuretic agent to improve liver function. However, the mechanism is not known for the liver-protective function. We investigated the antioxidant effects of plant extraction (CGE60) in vitro and in vivo, and find the mechanism of liver protection in Bacille Calmette-Guerin vaccine (BCG)+Lipopolysaccharides (LPS) induced liver injury in mice. MATERIALS AND METHODS: CGE60 was made, and the antioxidant activity was investigated by comparing the ability of scavenging 1,1-diphenyl-2-picrylhydrazyl (DPPH), and 2,2-azinobis(3-ehtylbenzothiazolin-6-sulfnicAcid) diammonium salt (ABTS) free radicals in vitro. Then, CGE60 was administrated in mice of liver damage model which was induced in mice using the BCG+LPS protocol. The CGE 60 extract was tested at three dosages: 50 mg/kg, 100 mg/kg, and 200 mg/kg. Product of lipid peroxidation (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-PX,), nitric oxide (NO), nitric oxide synthetase (NOS), hydroxyproline and alkaline phosphatase (ALP) contents were evaluated in liver to determine the CGE60 activity in the hepatic injury model. Tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and transforming growth factor-beta (TGF-beta) proteins were determined in the liver tissues using ELSIA. The signaling activities were evaluated in Western blot. RESULTS: CGE60 exhibited strong antioxidant ability in vitro. With oral administration, CGE60 significantly increased the activity of CAT, SOD, GSH-PX, and decreased the level of NO, NO synthase, hydroxyproline, ALP and lipid peroxidation liver of in the BDG+ LPS model. CGE60 attenuated hepatic inflammation via down- regulation of TNF-alpha, IL-6 and TGF-beta. CGE60 blocked protein expression of cytochrome P450 2E1 (CYP2E1), nuclear factor kappa-B (NF-kappaB), phosphorylation of extracellular signal-regulated kinase (p-ERK1/2), and cyclooxygenase-2 (COX-2),but activated the expression of p-P38 MAPK. CONCLUSION: This study suggests that CGE60 possesses antioxidant activity and this activity associates with hepatoprotective effect in the mice of BCG +LPS model, and the mechanisms underlying these effects may involve antioxidant actions and anti-inflammation activities. CI - Copyright (c) 2014. Published by Elsevier Ireland Ltd. FAU - Xin, Xuelei AU - Xin X AD - State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; Key Laboratory of Chemistry of Plant Resources in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China. FAU - Yang, Weijun AU - Yang W AD - State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; Key Laboratory of Chemistry of Plant Resources in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; Xinjiang Institute of material medic, Urumqi 830002, China. FAU - Yasen, Mireguli AU - Yasen M AD - State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; Key Laboratory of Chemistry of Plant Resources in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China. FAU - Zhao, Haiqing AU - Zhao H AD - State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; Key Laboratory of Chemistry of Plant Resources in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China. FAU - Aisa, Haji akber AU - Aisa Ha AD - State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China; Key Laboratory of Chemistry of Plant Resources in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20140613 PL - Ireland TA - J Ethnopharmacol JT - Journal of ethnopharmacology JID - 7903310 RN - 0 (Antioxidants) RN - 0 (Drugs, Chinese Herbal) RN - 0 (Plant Extracts) RN - 0 (Sesquiterpenes) SB - IM MH - Animals MH - Antioxidants/administration & dosage/isolation & purification/pharmacology MH - Asteraceae/*chemistry MH - Disease Models, Animal MH - Dose-Response Relationship, Drug MH - Drugs, Chinese Herbal/administration & dosage/chemistry/pharmacology MH - Female MH - Inflammation/drug therapy/pathology MH - Liver Diseases/immunology/*prevention & control MH - Male MH - Medicine, Chinese Traditional MH - Mice MH - Plant Extracts/administration & dosage/chemistry/*pharmacology MH - Sesquiterpenes/administration & dosage/isolation & purification/*pharmacology OTO - NOTNLM OT - Antiinflammation OT - Antioxidant OT - Cichorum glandulosum Boiss.et Huet OT - Hepatoprotective effect OT - Immune reaction-induced OT - liver injury EDAT- 2014/06/17 06:00 MHDA- 2015/10/23 06:00 CRDT- 2014/06/17 06:00 PHST- 2014/03/27 00:00 [received] PHST- 2014/05/15 00:00 [revised] PHST- 2014/06/04 00:00 [accepted] PHST- 2014/06/17 06:00 [entrez] PHST- 2014/06/17 06:00 [pubmed] PHST- 2015/10/23 06:00 [medline] AID - S0378-8741(14)00462-0 [pii] AID - 10.1016/j.jep.2014.06.014 [doi] PST - ppublish SO - J Ethnopharmacol. 2014 Sep 11;155(2):1068-75. doi: 10.1016/j.jep.2014.06.014. Epub 2014 Jun 13.