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芒果苷可预防肠道缺血/再灌注诱导的肝损伤:PPAR-γ、GSK-3β和Wnt/β-连环蛋白信号通路的作用

Mangiferin protects against ‭intestinal ischemia/reperfusion-induced ‭liver injury: ‬‬Involvement of PPAR-‭γ, GSK-3β and Wnt/β-catenin pathway‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬‬.

作者信息

El-Sayyad Shorouk M, Soubh Ayman A, Awad Azza S, El-Abhar Hanan S

机构信息

Department of Pharmacology & Toxicology, October 6 University,12585 Giza, Egypt.

Department of Pharmacology & Toxicology, Ahram Canadian University, 12566 Giza, Egypt.

出版信息

Eur J Pharmacol. 2017 Aug 15;809:80-86. doi: 10.1016/j.ejphar.2017.05.021. Epub 2017 May 12.

DOI:10.1016/j.ejphar.2017.05.021
PMID:28506911
Abstract

AIM

Mangiferin (MF), a xanthonoid from Mangifera indica, possesses anti-inflammatory, immunomodulatory, and potent antioxidant effects; however, its protective effect against mesenteric ischemia/reperfusion (I/R)-induced liver injury has not been fully clarified. The study was designed to assess the possible mechanism of action of MF against mesenteric I/R model.

MAIN METHODS

Male Wister rats were treated with MF (20mg/kg, i.p) or the vehicle for 3 days before I/R, which was induced by clamping the superior mesenteric artery for 30min followed by declamping for 60min.

KEY FINDINGS

The mechanistic studies revealed that MF protected the 2 organs studied, viz., liver and intestine partly via increasing the content of β-catenin and PPAR-γ along with decreasing that of GSK-3β and the phosphorylated NF-қB-p65. MF antioxidant effect was evidenced by increasing contents of total antioxidant capacity and GST, besides normalizing that of MDA. Regarding the anti-inflammatory effect, MF reduced IL-1β and IL-6, effects that were mirrored on the tissue content of MPO. Moreover, MF possessed anti-apoptotic character evidenced by elevating Bcl-2 content and reducing that of caspase-3. In the serum, intestinal I/R increased the activity of ALT, AST, and creatine kinase.

SIGNIFICANCE

The intimated protective mechanisms of MF against mesenteric I/R are mediated, partially, by modulation of oxidative stress, inflammation, and apoptosis possibly via the involvement of Wnt/β-catenin/NF-қβ/ PPAR-γ signaling pathways.

摘要

目的

芒果苷(MF)是一种从芒果中提取的呫吨酮类化合物,具有抗炎、免疫调节和强大的抗氧化作用;然而,其对肠系膜缺血/再灌注(I/R)诱导的肝损伤的保护作用尚未完全阐明。本研究旨在评估MF对肠系膜I/R模型的可能作用机制。

主要方法

雄性Wistar大鼠在I/R前3天接受MF(20mg/kg,腹腔注射)或溶剂处理,I/R通过夹闭肠系膜上动脉30分钟,然后松开60分钟诱导。

主要发现

机制研究表明,MF对所研究的两个器官,即肝脏和肠道具有保护作用,部分是通过增加β-连环蛋白和PPAR-γ的含量,同时降低GSK-3β和磷酸化NF-қB-p65的含量。除了使丙二醛含量正常化外,总抗氧化能力和谷胱甘肽S-转移酶含量的增加证明了MF的抗氧化作用。关于抗炎作用,MF降低了IL-1β和IL-6,这些作用反映在髓过氧化物酶的组织含量上。此外,MF具有抗凋亡特性,表现为Bcl-2含量升高和caspase-3含量降低。在血清中,肠道I/R增加了ALT、AST和肌酸激酶的活性。

意义

MF对肠系膜I/R的保护机制可能部分是通过Wnt/β-连环蛋白/NF-қβ/PPAR-γ信号通路调节氧化应激、炎症和细胞凋亡来介导的。

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