Atraric Acid Exhibits Anti-Inflammatory Effect in Lipopolysaccharide-Stimulated RAW264.7 Cells and Mouse Models.
Seul-Ki MunKyung-Yun KangHo-Yeol JangYun-Ho HwangSeong-Gyeol HongSu-Jin KimHyun-Wook ChoDong-Jo ChangJae-Seoun HurSung-Tae YeePublished in: International journal of molecular sciences (2020)
Lichens, composite organisms resulting from the symbiotic association between the fungi and algae, produce a variety of secondary metabolites that exhibit pharmacological activities. This study aimed to investigate the anti-inflammatory activities of the secondary metabolite atraric acid produced by Heterodermia hypoleuca. The results confirmed that atraric acid could regulate induced pro-inflammatory cytokine, nitric oxide, prostaglandin E2, induced nitric oxide synthase and cyclooxygenase-2 enzyme expression in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Meanwhile, atraric acid downregulated the expression of phosphorylated IκB, extracellular signal-regulated kinases (ERK) and nuclear factor kappa B (NFκB) signaling pathway to exhibit anti-inflammatory effects in LPS-stimulated RAW264.7 cells. Based on these results, the anti-inflammatory effect of atraric acid during LPS-induced endotoxin shock in a mouse model was confirmed. In the atraric acid treated-group, cytokine production was decreased in the peritoneum and serum, and each organ damaged by LPS-stimulation was recovered. These results indicate that atraric acid has an anti-inflammatory effect, which may be the underlying molecular mechanism involved in the inactivation of the ERK/NFκB signaling pathway, demonstrating its potential therapeutic value for treating inflammatory diseases.
Keyphrases
- anti inflammatory
- signaling pathway
- lps induced
- induced apoptosis
- nuclear factor
- inflammatory response
- pi k akt
- nitric oxide
- mouse model
- toll like receptor
- cell cycle arrest
- nitric oxide synthase
- oxidative stress
- epithelial mesenchymal transition
- poor prognosis
- cell proliferation
- immune response
- ms ms
- endoplasmic reticulum stress
- transcription factor
- newly diagnosed
- drug induced
- gram negative