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首页> 外文期刊>International immunopharmacology >Chlorogenic acid ameliorated concanavalin A-induced hepatitis by suppression of Toll-like receptor 4 signaling in mice
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Chlorogenic acid ameliorated concanavalin A-induced hepatitis by suppression of Toll-like receptor 4 signaling in mice

机译:通过抑制小鼠中的信号传导4信号传导,通过抑制诱导的胰岛原酸诱导的肝炎。

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Chlorogenic acid (CGA), one of the most abundant dietary polyphenolic compounds, has been reported to exhibit anti-inflammatory ability. However, the hepatoprotective effects and molecular mechanisms of CGA on concanavalin A (Con A)-induced hepatitis have not been explored. In the present study, we found that pretreatment with CGA dose-dependently inhibited the elevation of plasma aminotransferases and alleviated hepatic pathological damage as well as hepatocyte apoptosis in Con A-exposed mice. Additionally, CGA markedly suppressed the production of serum tumor necrosis factor (TNF)-alpha and interferon (IFN)-gamma, alleviated the infiltration of hepatic macrophages, neutrophils, and activated CD4(+) T lymphocytes in Con A-primed mice. Moreover, CGA down regulated Con A -induced hepatic expression of adhesion molecules (ICAM-1, VCAM-1 and ELAM-1) mRNA and protein, and inhibited Con A-activated Toll-like receptor (TLR) 4 signal molecules including TLR4, p-IRAKI, p-KB, and p-p38. Finally, our results also showed that CGA exhibited a therapeutic effect, which CGA posttreatment improved hepatic damage at 1, 3, and 6 h after Con A. Taken together, these data suggested that CGA could effectively prevent mice from Con A -induced hepatitis, which might be through suppressing the activation of TLR4 signaling, downregulating the expression of adhesion molecules, and alleviating the infiltration and activation of hepatic leukocytes and the production of pro-inflammatory cytokines. (C) 2017 Elsevier B.V. All rights reserved.
机译:据报道,绿原酸(CGA)是最丰富的膳食多酚化合物之一表现出抗炎能力。然而,尚未探讨CGA对CGA的肝脏保护作用和分子机制 - 诱导的肝炎诱导的肝炎。在本研究中,我们发现与CGA剂量的预处理依赖性抑制血浆氨基转移酶的升高,并缓解了肝脏病理损伤以及CON暴露小鼠中的肝细胞凋亡。此外,CGA显着抑制了血清肿瘤坏死因子(TNF) - α和干扰素(IFN)-Gamma的生产,缓解了肝巨噬细胞,中性粒细胞和活化CD4(+)T淋巴细胞的渗透,CO-Primed小鼠。此外,CGA下调CON-诱导粘附分子的肝脏表达(ICAM-1,VCAM-1和ELAM-1)mRNA和蛋白,并抑制CON激活的Toll样受体(TLR)4个信号分子,包括TLR4, p-araki,p-kb和p-p38。最后,我们的结果还表明CGA表现出治疗效果,CGA患者在CON A中提高了肝脏损伤,在CON A中提高了肝脏损伤。在一起,这些数据表明CGA可以有效地防止来自CON诱导的肝炎的小鼠,这可能是通过抑制TLR4信号传导的激活,下调粘附分子的表达,并减轻肝白细胞的渗透和活化和促炎细胞因子的产生。 (c)2017 Elsevier B.v.保留所有权利。

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