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獐牙菜苦苷萜类丰富部位对免疫反应性肝损伤的保肝作用机制。

The mechanism of hepatoprotective effect of sesquiterpene rich fraction from Cichorum glandulosum Boiss. et Huet on immune reaction-induced liver injury in mice.

机构信息

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.

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.

出版信息

J Ethnopharmacol. 2014 Sep 11;155(2):1068-75. doi: 10.1016/j.jep.2014.06.014. Epub 2014 Jun 13.

Abstract

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-α), interleukin-6 (IL-6) and transforming growth factor-β (TGF-β) 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-α, IL-6 and TGF-β. CGE60 blocked protein expression of cytochrome P450 2E1 (CYP2E1), nuclear factor kappa-B (NF-κB), 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.

摘要

民族药理学相关性

腺毛蓝刺头(Cichorum glandulosum Boiss. et Huet)是一种传统的维吾尔草药,已被用作利胆和利尿药,以改善肝功能。然而,其保肝作用的机制尚不清楚。我们研究了植物提取物(CGE60)在体外和体内的抗氧化作用,并发现了卡介苗(BCG)+脂多糖(LPS)诱导的肝损伤小鼠中肝保护的机制。

材料和方法

制备 CGE60,并通过比较清除 1,1-二苯基-2-苦基肼(DPPH)和 2,2-联氮-双(3-乙基苯并噻唑啉-6-磺酸)二铵盐(ABTS)自由基的能力,体外研究其抗氧化活性。然后,用 BCG+LPS 方案诱导肝损伤模型的小鼠给予 CGE60 提取物。在肝损伤模型中,测试 CGE60 提取物的三个剂量:50mg/kg、100mg/kg 和 200mg/kg。测定肝组织中丙二醛(MDA)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-PX)、一氧化氮(NO)、一氧化氮合酶(NOS)、羟脯氨酸和碱性磷酸酶(ALP)的含量,以确定 CGE60 在肝损伤模型中的活性。采用酶联免疫吸附法(ELISA)测定肝组织中肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和转化生长因子-β(TGF-β)蛋白的含量。通过 Western blot 评估信号转导活性。

结果

CGE60 表现出体外强抗氧化能力。口服 CGE60 可显著提高 CAT、SOD、GSH-PX 的活性,降低 BCG+LPS 模型中 NO、NOS、羟脯氨酸、ALP 和脂质过氧化的水平。CGE60 通过下调 TNF-α、IL-6 和 TGF-β 来减轻肝炎症。CGE60 阻断细胞色素 P450 2E1(CYP2E1)、核因子 kappa-B(NF-κB)、细胞外信号调节激酶(p-ERK1/2)和环加氧酶-2(COX-2)的蛋白表达,但激活 p-P38 MAPK 的表达。

结论

本研究表明,CGE60 具有抗氧化活性,这种活性与 BCG+LPS 模型小鼠的保肝作用有关,其作用机制可能涉及抗氧化作用和抗炎作用。

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