首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Effect of sinomenine on cytokine expression of macrophages and synoviocytes in adjuvant arthritis rats.
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Effect of sinomenine on cytokine expression of macrophages and synoviocytes in adjuvant arthritis rats.

机译:青藤碱对佐剂性关节炎大鼠巨噬细胞和滑膜细胞细胞因子表达的影响。

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For exploring the mechanism of the anti-inflammatory and anti-rheumatic effect of sinomenine (SN), the actions of different dosage of SN were observed in vitro on the expression of cytokines, tumor necrosis factor (TNF-alpha) and interleukin-1beta (IL-1beta), as well as the activity of nuclear factor-kappaB (NF-kappaB) and the inhibitory kappaB-alpha (IkappaB-alpha) protein level of peritoneal macrophages (PMs) and synoviocytes in adjuvant arthritis (AA) rats. In this study, the experimental rat model of AA was used and PMs and synoviocytes were collected. The mRNAs of TNF-alpha and IL-1beta were detected with reverse transcription-polymerase chain reaction (RT-PCR) and NF-kappaB activity was measured by electrophoretic mobility shift assay (EMSA). The IkappaB-alpha protein level in the cytoplasma was detected by Western blot. Our results showed that expression of mRNAs of TNF-alpha and IL-1beta and NF-kappaB activity by PMs and synoviocytes were markedly increased compared to control group (P<0.05). In a definite concentration ranging from 30 to 120mug/ml, SN showed inhibiting effect on the NF-kappaB activity and the expression of the mRNAs of TNF-alpha and IL-1beta in AA rats in a concentration-dependent manner (P<0.05). Positive correlations were found between changes of NF-kappaB activity and expression of TNF-alpha mRNA and IL-1beta mRNA (P<0.01). IkappaB-alpha protein level was increased by various dosages of SN in comparison with control group (P<0.01). In conclusion, SN decreases the mRNA expression of TNF-alpha and IL-1beta by inhibiting the NF-kappaB binding activity, which is mediated through up-regulating the IkappaB-alpha expression of PMs and synoviocytes in AA rats.
机译:为了探讨青藤碱(SN)的抗炎和抗风湿作用的机制,我们在体外观察了不同剂量的SN对细胞因子,肿瘤坏死因子(TNF-α)和白介素-1β( IL-1beta)以及佐剂性关节炎(AA)大鼠腹膜巨噬细胞(PMs)和滑膜细胞的核因子-κB(NF-kappaB)活性和抑制性kappaB-alpha(IkappaB-alpha)蛋白水平。在这项研究中,使用了AA的实验大鼠模型,并收集了PM和滑膜细胞。逆转录-聚合酶链反应(RT-PCR)检测TNF-α和IL-1β的mRNA,电泳迁移率变动分析(EMSA)检测NF-κB的活性。通过Western印迹检测细胞质中的IkappaB-α蛋白水平。我们的结果表明,与对照组相比,PMs和滑膜细胞的TNF-α和IL-1beta的mRNA表达和NF-κB活性显着增加(P <0.05)。在30-120μg/ ml的一定浓度下,SN对AA大鼠的NF-κB活性以及TNF-α和IL-1βmRNA的表达呈浓度依赖性(P <0.05)。 。 NF-κB活性的变化与TNF-α和IL-1β的表达呈正相关(P <0.01)。与对照组相比,不同剂量的SN可增加IkappaB-α蛋白水平(P <0.01)。总之,SN通过抑制NF-kappaB结合活性来降低TNF-α和IL-1beta的mRNA表达,这是通过上调AA大鼠PMs和滑膜细胞的IkappaB-alpha表达来介导的。

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