首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Effects of Chaihu-Shugan-San and Shen-Ling-Bai-Zhu-San on p38 MAPK Pathway in Kupffer Cells of Nonalcoholic Steatohepatitis
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Effects of Chaihu-Shugan-San and Shen-Ling-Bai-Zhu-San on p38 MAPK Pathway in Kupffer Cells of Nonalcoholic Steatohepatitis

机译:柴湖 - 蜀山 - 沉竹 - 珠 - 朱哲 - 在非酒精性脂肪肝炎的Kupffer细胞中P38 Mapk途径的影响

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This study aimed to investigate the effects of Chaihu-Shugan-San (CSS), Shen-Ling-Bai-Zhu-San (SLBZS), and integrated recipe of the above two recipes on inflammatory markers and proteins involved in p38 MAPK pathway in Kupffer cells of NASH rats induced by high fat diet (HFD). Rats were administered at low or high dose of CSS, SLBZS, and integrated recipe except normal group and model group for 16 weeks. The levels of hepatic lipid, TNF-α, IL-1, and IL-6 in liver tissues were measured. Kupffer cells were isolated from livers to evaluate expressions of TLR4, p-p38 MAPK, and p38 MAPK by Western blotting. The results showed that the NASH model rats successfully reproduced typical pathogenetic and histopathological features. Levels of hepatic lipid and liver tissues inflammatory factors in high-dose SLBZS group and integrated recipe group were all lower than that of model group decreased observably. Expressions of TLR4, p-p38 MAPK, and p38 MAPK in Kupffer cells were decreased in all treatment groups, but there was no significant difference between treatment groups. The high-dose SLBZS group had the lowest expression levels of TLR4, and the most visible downtrend in the expression levels of p-p38 MAPK and p38 MAPK was found in the high-dose integrated recipe group. The ratio of p-p38 MAPK to total p38 MAPK protein was obviously increased in all treatment groups. Therefore, our study showed that the activation of p38 MAPK pathway in Kupffer cells might be related to the release of inflammatory factors such as TNF-α, IL-1, and IL-6 in NASH rats. High dose of SLBZS and integrated recipe might work as a significant anti-inflammatory effect in Kupffer cells of NASH rats induced by HFD through suppression of p38 MAPK pathway. It indicated that p38 MAPK pathway may be the possible effective target for the recipes.
机译:本研究旨在探讨柴胡舒甘 - 圣(CSS),沉岭白竹 - San(SLBZS)的影响,以及上述两种食谱的炎症标志物和蛋白质中参与Kupffer的蛋白质的综合配方高脂饮食(HFD)诱导的肿瘤大鼠细胞。除正常组和模型组外,在低剂量或高剂量的CSS,SLBZ和综合配方中施用大鼠16周。测量肝脏组织中肝脂,TNF-α,IL-1和IL-6的水平。通过蛋白质印迹,从肝脏中分离出Kupffer细胞以评估TLR4,P-P38 MAPK和P38 MAPK的表达。结果表明,纳什模型大鼠成功地复制了典型的致病和组织病理学特征。高剂量SLBZS组和综合配方组肝脂和肝脏组织炎症因子的水平均低于模型组显着降低的因素。在所有治疗组中,Kupffer细胞中TLR4,P-P38 MAPK和P38 MAPK的表达,但治疗组之间没有显着差异。高剂量SLBZS组具有TLR4的最低表达水平,并且在高剂量集成配方组中发现了P-P38 MAPK和P38 MAPK的表达水平中最明显的下降趋势。所有治疗组明显增加P-P38 MAPK至总P38 MAPK蛋白的比例。因此,我们的研究表明,Kupffer细胞中P38 MAPK途径的激活可能与肿瘤大鼠中TNF-α,IL-1和IL-6等炎症因子的释放有关。通过抑制P38Mapk途径,高剂量的SLBZS和综合配方可能在HFD诱导的NAHFER大鼠Kupffer细胞中作用于Kupffer细胞的显着抗炎作用。它表明P38 MAPK路径可能是食谱的可能有效目标。

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