AI Article Synopsis

  • Liang-Ge-San (LGS) is a traditional Chinese medicine formula known for its use in treating conditions like acute lung injury and throat infections, but its mechanisms were not well understood until now.
  • This study found that LGS has strong anti-inflammatory properties, significantly reducing the production of harmful inflammatory markers like IL-6 and TNF-α in lab tests with macrophage cells and in rat models of acute lung injury.
  • The research highlights the role of the α7 nicotinic cholinergic receptor in these effects, suggesting that LGS activates this receptor to inhibit inflammation, thus offering a foundation for its clinical use as an anti-inflammatory agent.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008280PMC
http://dx.doi.org/10.18632/oncotarget.8452DOI Listing

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