首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Combinatorial usage of fungal polysaccharides from Cordyceps sinensis and Ganoderma atrum ameliorate drug-induced liver injury in mice
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Combinatorial usage of fungal polysaccharides from Cordyceps sinensis and Ganoderma atrum ameliorate drug-induced liver injury in mice

机译:来自冬虫夏草的真菌多糖的组合使用和灵芝胃炎改善药物诱导的小鼠肝损伤

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摘要

This study investigated the possible protective effect of combined fungal polysaccharides (CFP), consisting ofCordyceps sinensispolysaccharides (CSP) andGanoderma atrumpolysaccharides (PSG) with well-defined structural characteristics, against cyclophosphamide (CTX)-induced hepatotoxicity in mice. Our results indicated CFP effectively prevented the liver injury by decreasing toxicity markers (aspartate transaminase, alanine aminotransferase and alkaline phosphatase). Further biochemical and molecular analysis indicated CSP particularly inhibited the activation of Toll-like receptor 9 (TLR9) and its related inflammatory signals, including pro-inflammatory cytokines, inducible nitric oxide synthase, and cyclooxygenase-2 to modulate hepatic inflammation response. Relatively, through activation of peroxisome proliferator-activated receptor α (PPARα), PSG increased hepatic glutathione peroxidase and glutathione content depleted by CTX, as well as prevented mitochondria-dependent apoptosis with regulation on Bcl-2 family proteins (Bad, Bax and Bcl-2). In addition, protective effect of CFP was associated with enhanced modulations on cellular oxidant/antioxidant imbalance, mitochondrial apoptotic pathway and pro-inflammatory factors via PPARα upregulation and TLR9 downregulation. Taking together, the combinatorial approach based on CSP and PSG presented a practical option for the management of drug-induced liver injury.
机译:本研究研究了组合真菌多糖(CSP)(CSP)和甘露霉菌酸酐(PSG)的组合真菌多糖(CSP)和钯),其具有良好定义的结构特征,对小鼠的肝毒性诱导的肝毒性诱导的结构特征组成。我们的结果表明,CFP通过减少毒性标志物(天冬氨酸转氨酶,丙氨酸转氨酶,丙氨酸氨基转移酶和碱性磷酸酶)有效地防止了肝损伤。进一步的生物化学和分子分析表明CSP特别抑制了可抑制了Toll样受体9(TLR9)的激活及其相关的炎症信号,包括促炎细胞因子,诱导型一氧化氮合酶和环氧化酶-2以调节肝脏炎症反应。相对而言,通过激活过氧化物体增殖物激活受体α(PPARα),PSG增加了CTX耗尽的肝谷胱甘肽过氧化物酶和谷胱甘肽含量,以及预防的线粒体依赖性细胞凋亡与Bcl-2家族蛋白(坏,Bax和Bcl- 2)。此外,通过PPARα上调和TLR9下调,CFP对细胞氧化剂/抗氧化不平衡,线粒体凋亡途径和促炎因子的增强的调节有关。在一起,基于CSP和PSG的组合方法提出了用于药物诱导的肝损伤的实际选择。

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