Xiong-Zhe Han1, Rui Ma2, Qi Chen3, Xin Jin4, Yuan-Zhe Jin5, Ren-Bo An6, Xuan-Mei Piao7, Mei-Lan Lian8, Lin-Hu Quan9, Jun Jiang10. 1. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: 1654766679@qq.com. 2. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: 511567534@qq.com. 3. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: 731042970@qq.com. 4. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: 1547084639@qq.com. 5. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: Y-z-jin@ybu.edu.cn. 6. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: 1484536370@qq.com. 7. Department of Urology, College of Medicine, Chungbuk National University, Cheongju 28644, Republic of Korea. Electronic address: Phm1013@hotmail.com. 8. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: Lianmeilan2001@163.com. 9. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: Lhquan@ybu.edu.cn. 10. Key Laboratory of Natural Resource of Changbai Mountain and Functional Molecules (Ministry of Education), Ginseng Research Center of Changbai Mountain, Yanbian University, Yanji 133002, Jilin, China. Electronic address: Jiangjun@ybu.edu.cn.
Abstract
ETHNOPHARMACOLOGICAL RELEVANCE: The aerial part of Athyrium multidentatum (Doll.) Ching (AM) is widely used in the northeastern region of China as an edible wild herb, but its medicinal value, especially its anti-inflammatory effect, has not been fully explored. AIM OF THE STUDY: To investigate the anti-inflammatory activity of AM and clarify the anti-inflammatory mechanism involving the TLR4 signaling pathway using a lipopolysaccharide (LPS)-induced inflammatory model. MATERIALS AND METHODS: AM ethanol extract was used as the experimental material to investigate the effect that the extract has on the production of pro-inflammatory mediators (NO, PGE2, TNF-α, IL-1β and IL-6); changes in LPS-induced peritoneal macrophages (PMs); and TLR4-mediated intracellular events, including MAPKs (ERK, JNK, and p38) and IκB-α in the MyD88-dependant pathway and IRF3, STAT1, and STAT3 in the TRIF-dependent pathway. In in vivo experiments, we established an LPS-induced acute lung injury (ALI) model and investigated the cell count and cytokine (TNF-α, IL-1β and IL-6) levels in bronchoalvelar lavage fluid (BALF) of C57BL6 mice. Histological changes in the lung tissues were observed with H&E staining. RESULTS: AM extract inhibited NO and PGE2 by suppressing their synthetase (iNOS and COX-2) gene expression in LPS-induced PMs; the secretion of IL-6, IL-1β, and TNF-α also deceased via the down-regulation of mRNA levels. Furthermore, the TLR4-mediated intracellular events involved the phosphorylated forms of MAPKs (ERK, JNK) and IκB-α in the MyD88-dependent pathway and the TRIF-dependent pathway (IRF3, STAT1, STAT3), and the relevant proteins were expressed at low levels in the AM extract groups. In in vivo experiments, the cell count and cytokine (TNF-α, IL-1β and IL-6) levels in BALF decreased significantly in a dose-dependent manner in the AM extract groups. The lung tissue structure exhibited dramatic damage in the LPS group, and the damaged area decreased in the AM extract groups; in particular, the effect of 10 mg/kg extract was similar to that of the positive control dexamethasone (DEX). CONCLUSION: The findings demonstrate that AM protects against LPS-induced acute lung injury by suppressing TLR4 signaling, provide scientific evidence to support further study of the safety of anti-inflammatory drugs and indicate that AM can be used as an anti-inflammatory and anti-injury agent to prevent pneumonia caused by microbial infection.
ETHNOPHARMACOLOGICAL RELEVANCE: The aerial part of Athyrium multidentatum (Doll.) Ching (AM) is widely used in the northeastern region of China as an edible wild herb, but its medicinal value, especially its anti-inflammatory effect, has not been fully explored. AIM OF THE STUDY: To investigate the anti-inflammatory activity of AM and clarify the anti-inflammatory mechanism involving the TLR4 signaling pathway using a lipopolysaccharide (LPS)-induced inflammatory model. MATERIALS AND METHODS: AM ethanol extract was used as the experimental material to investigate the effect that the extract has on the production of pro-inflammatory mediators (NO, PGE2, TNF-α, IL-1β and IL-6); changes in LPS-induced peritoneal macrophages (PMs); and TLR4-mediated intracellular events, including MAPKs (ERK, JNK, and p38) and IκB-α in the MyD88-dependant pathway and IRF3, STAT1, and STAT3 in the TRIF-dependent pathway. In in vivo experiments, we established an LPS-induced acute lung injury (ALI) model and investigated the cell count and cytokine (TNF-α, IL-1β and IL-6) levels in bronchoalvelar lavage fluid (BALF) of C57BL6 mice. Histological changes in the lung tissues were observed with H&E staining. RESULTS: AM extract inhibited NO and PGE2 by suppressing their synthetase (iNOS and COX-2) gene expression in LPS-induced PMs; the secretion of IL-6, IL-1β, and TNF-α also deceased via the down-regulation of mRNA levels. Furthermore, the TLR4-mediated intracellular events involved the phosphorylated forms of MAPKs (ERK, JNK) and IκB-α in the MyD88-dependent pathway and the TRIF-dependent pathway (IRF3, STAT1, STAT3), and the relevant proteins were expressed at low levels in the AM extract groups. In in vivo experiments, the cell count and cytokine (TNF-α, IL-1β and IL-6) levels in BALF decreased significantly in a dose-dependent manner in the AM extract groups. The lung tissue structure exhibited dramatic damage in the LPS group, and the damaged area decreased in the AM extract groups; in particular, the effect of 10 mg/kg extract was similar to that of the positive control dexamethasone (DEX). CONCLUSION: The findings demonstrate that AM protects against LPS-induced acute lung injury by suppressing TLR4 signaling, provide scientific evidence to support further study of the safety of anti-inflammatory drugs and indicate that AM can be used as an anti-inflammatory and anti-injury agent to prevent pneumonia caused by microbial infection.