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首页> 外文期刊>Biological & pharmaceutical bulletin >Effects of S/B Remedy Containing Scutellaria baicalensis and Bupleurum scorzonerifolfium on Hepatic Interleukin-6 Related Signal Transducer and Activator of Transcription 3 Activation in Mice through Cell-Cell Interaction
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Effects of S/B Remedy Containing Scutellaria baicalensis and Bupleurum scorzonerifolfium on Hepatic Interleukin-6 Related Signal Transducer and Activator of Transcription 3 Activation in Mice through Cell-Cell Interaction

机译:黄S和柴胡柴胡的S / B疗法对小鼠肝细胞白细胞介素6相关信号转导和转录3激活因子的影响

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摘要

Signal transducer and activator of transcription 3 (STAT3) plays an important role in regulating interleukin 6 (IL-6) related growth control of the liver. Our previous study demonstrated that a mixture containing Scutellaria baicalensis and Bupleurum scorzonerifolfium (S/B remedy) modulated the growth of hepatocytes during liver regeneration after 2/3 partial hepatectomy. The aim of this study was to investigate whether S/B remedy induced mouse hepatic STAT3 activation directly in hepatocytes or indirectly via non-parenchymal cell hepatocyte interaction. Direct S/B remedy effects were studied using primarily isolated hepatocytes; while C57BL/6J mice were used to study indirect effects of S/B remedy using gadolinium chloride to deplete Kupffer cells' function. The results showed that SIB remedy and its active constituents did not directly activate growth-related signaling in primarily isolated hepatocytes. However, S/B remedy induced STAT3 and subsequently suppressor of cytokine signaling (SOCS3) activation in mouse liver and increased serum IL-6 level in a dose-dependent manner, which could be partially blocked by pretreatment with gadolinium chloride. Oligonucloetide microarray analysis from S/B remedy-treated peripheral blood leukocytes demonstrated an up-regulation of IL-6 gene expression. We conclude that S/B remedy did not directly induce STAT3 activation in vitro, but induced hepatic IL-6 related STAT3 activation through non-parenchymal cell-hepatocyte interaction in vivo. The results provide important information on the molecular mechanisms of S/B remedy for treatment of human liver diseases.
机译:信号转导和转录激活因子3(STAT3)在调节白介素6(IL-6)相关的肝脏生长控制中起重要作用。我们之前的研究表明,在2/3部分肝切除术后肝脏再生期间,含有黄dy和柴胡(S / B补救)的混合物可调节肝细胞的生长。这项研究的目的是调查S / B补救措施是否直接在肝细胞中或通过非实质细胞与肝细胞的相互作用间接诱导小鼠肝STAT3活化。使用主要分离的肝细胞研究了直接S / B补救作用; C57BL / 6J小鼠用于研究氯化/对S / B疗法的间接作用,以耗尽库普弗细胞的功能。结果表明,SIB药物及其有效成分并未直接激活主要分离的肝细胞中与生长相关的信号。但是,S / B补救措施可诱导STAT3,随后抑制小鼠肝脏中的细胞因子信号传导(SOCS3)活化,并以剂量​​依赖的方式增加血清IL-6水平,这可能会被氯化g预处理部分地阻断。 S / B药物治疗的外周血白细胞的寡核苷酸微阵列分析表明,IL-6基因表达上调。我们得出的结论是,S / B补救措施并没有直接在体外诱导STAT3激活,而是通过体内非实质细胞与肝细胞的相互作用诱导了与肝脏IL-6相关的STAT3激活。该结果提供了有关S / B疗法治疗人类肝脏疾病的分子机制的重要信息。

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