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Protective Effect of Gallotannin-Enriched Extract Isolated from Galla Rhois against CCl 4 -Induced Hepatotoxicity in ICR Mice

机译:从五倍子中分离得到的富含gallotannin的提取物对ICR小鼠的CCl 4诱导的肝毒性的保护作用

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To investigate the toxicity, protective effects, and action mechanism of gallotannin-enriched extracts isolated from Galla Rhois (GEGR) against carbon tetrachloride (CCl 4 )-induced hepatotoxicity in Institute for Cancer Research (ICR) mice, alterations in serum biochemical indicators, histopathological structure, antioxidative status, hepatic apoptosis-related proteins, and liver fibrosis regulating factors were measured in mice pretreated with GEGR for five days before CCl 4 injection. The GEGR/CCl 4 treated group showed decreased levels of three serum marker enzymes (ALP, AST, and ALT) representing liver toxicity, although LDH levels remained constant. Necrotic area indicating hepatic cell death significantly inhibited, while malondialdehyde (MDA) concentration and superoxide dismutase (SOD) expression were dramatically recovered in the GEGR preadministrated group. In mechanism analyses of GEGR, the formation of active caspase-3 and enhancement of Bax/Bcl-2 expression was effectively inhibited in the GEGR/CCl 4 treated group. The level of pro-inflammatory cytokines, TNF-α and IL-6, as well as the phosphorylation of p38 and JNK in the TNF-α downstream signaling pathway was rapidly recovered in the GEGR/CCl 4 treated group, while anti-inflammatory cytokine (IL-10) increased slightly in the same group. Furthermore, the GEGR/CCl 4 treated group showed a significant decrease in collagen accumulation results from alleviation of MMP-2 expression, TGF-β1 secretion and the phosphorylation of Smad2/3. Taken together, these results suggest that GEGR may induce remarkable protective effects against hepatic injury induced by CCl 4 treatment through upregulation of the anti-inflammatory and antioxidant system.
机译:研究从加勒罗伊斯(GEGR)中分离出的富含Gallantannin的提取物对四氯化碳(CCl 4)诱导的癌症研究所(ICR)小鼠肝毒性,血清生化指标变化,组织病理学的毒性,保护作用和作用机理在注射CCl 4前五天,用GEGR预处理的小鼠中测量了其结构,抗氧化状态,肝细胞凋亡相关蛋白和肝纤维化调节因子。尽管LDH水平保持恒定,但GEGR / CCl 4处理组显示出三种代表肝脏毒性的血清标志物酶(ALP,AST和ALT)水平降低。预先给予GEGR的组可显着抑制表明肝细胞死亡的坏死区域,同时显着恢复丙二醛(MDA)浓度和超氧化物歧化酶(SOD)表达。在GEGR的机理分析中,在GEGR / CCl 4处理组中有效抑制了caspase-3活性的形成和Bax / Bcl-2表达的增强。在GEGR / CCl 4处理组中,迅速恢复了促炎细胞因子,TNF-α和IL-6的水平,以及TNF-α下游信号通路中p38和JNK的磷酸化,而消炎细胞因子同一组中的(IL-10)略有增加。此外,GEGR / CCl 4处理组由于减轻了MMP-2的表达,TGF-β1的分泌和Smad2 / 3的磷酸化而显示出胶原蛋白积聚的显着减少。综上所述,这些结果表明,GEGR可以通过上调抗炎和抗氧化系统,诱导出显着的抗CCl 4处理所致肝损伤的保护作用。

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