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Liang-Ge-San a classic traditional Chinese medicine formula protects against lipopolysaccharide-induced inflammation through cholinergic anti-inflammatory pathway

机译:梁格三一种经典的传统中药配方可通过胆碱能抗炎途径防止脂多糖引起的炎症

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摘要

Liang-Ge-San (LGS) is a classic formula in traditional Chinese medicine, which is widely used to treat acute lung injury (ALI), pharyngitis and amygdalitis in clinic. However, the underlying mechanisms remain poorly defined. In this study, we discovered that LGS exerted potent anti-inflammatory effects in lipopolysaccharide (LPS)-induced inflammation. We found that LGS significantly depressed the production of IL-6 and TNF-α in LPS-stimulated RAW 264.7 macrophage cells. The degradation and phosphorylation of IκBα and the nuclear translocation of NF-κB p65 were also inhibited. Moreover, LGS activated α7 nicotinic cholinergic receptor (α7nAchR). The blockage of α7nAchR by selective inhibitor methyllycaconitine (MLA) or α7nAchR siRNA attenuated the inhibitory effects of LGS on IκBα, NF-κB p65, IL-6 and TNF-α. Critically, LGS significantly inhibited inflammation in LPS-induced ALI rats through the activation of NF-κB signaling pathway. However, these protective effects could be counteracted by the treatment of MLA. Taken together, we first demonstrated anti-inflammatory effects of LGS both in vitro and in vivo through cholinergic anti-inflammatory pathway. The study provides a rationale for the clinical application of LGS as an anti-inflammatory agent and supports the critical role of cholinergic anti-inflammatory pathway in inflammation.
机译:梁格三(LGS)是传统中药的经典配方,在临床上被广泛用于治疗急性肺损伤(ALI),咽炎和扁桃体炎。但是,基本机制仍然定义不清。在这项研究中,我们发现LGS在脂多糖(LPS)诱导的炎症中发挥了有效的抗炎作用。我们发现LGS显着抑制LPS刺激的RAW 264.7巨噬细胞中IL-6和TNF-α的产生。 IκBα的降解和磷酸化以及NF-κBp65的核易位也受到抑制。此外,LGS激活了α7烟碱胆碱能受体(α7nAchR)。选择性抑制剂甲基lycaconitine(MLA)或α7nAchRsiRNA阻断α7nAchR减弱了LGS对IκBα,NF-κBp65,IL-6和TNF-α的抑制作用。至关重要的是,LGS通过激活NF-κB信号通路显着抑制LPS诱导的ALI大鼠的炎症。但是,MLA的治疗可以抵消这些保护作用。两者合计,我们首先通过胆碱能抗炎途径证明了LGS在体外和体内的抗炎作用。该研究为LGS作为抗炎药的临床应用提供了理论依据,并支持胆碱能抗炎途径在炎症中的关键作用。

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