Anti-inflammatory effects of Flos Lonicerae Japonicae Water Extract are regulated by the STAT/NF-κB pathway and HO-1 in Virus-infected RAW264.7 cells

被引:31
作者
Lin, Hui-Wen [1 ,2 ,3 ]
Lee, Yi-Ju [4 ,5 ]
Yang, Deng-Jye [6 ]
Hsieh, Ming-Chang [7 ,8 ]
Chen, Ching-Chung [1 ]
Hsu, Wei-Li [9 ]
Chang, Yuan-Yen [8 ,10 ,11 ]
Liu, Cheng-Wei [12 ]
机构
[1] Asia Univ, Dept Optometry, Taichung, Taiwan
[2] China Med Univ, China Med Univ Hosp, Genet Ctr, Dept Med Res, Taichung, Taiwan
[3] China Med Univ, Sch Chinese Med, Taichung, Taiwan
[4] Chung Shan Med Univ, Dept Pathol, Taichung, Taiwan
[5] Chung Shan Med Univ Hosp, Dept Pathol, Taichung, Taiwan
[6] Natl Yang Ming Univ, Inst Food Safety & Hlth Risk Assessment, Taipei, Taiwan
[7] Chung Shan Med Univ, Dept Med Lab & Biotechnol, Taichung, Taiwan
[8] Chung Shan Med Univ Hosp, Clin Lab, Taichung, Taiwan
[9] Natl Chung Hsing Univ, Coll Vet Med, Grad Inst Microbiol & Publ Hlth, Taichung, Taiwan
[10] Sch Med, Dept Microbiol & Immunol, Taichung, Taiwan
[11] Chung Shan Med Univ, Taichung, Taiwan
[12] MingDao Univ, Dept Postmodern Agr, Changhua, Taiwan
关键词
Flos Lonicerae Japonicae water extract (FLJWE); pseudorabies virus (PRV); antiviral inflammatory; heme oxygenase-1 (HO-1); INDUCED INFLAMMATORY RESPONSE; SALINA ALGA EXTRACT; NITRIC-OXIDE; DOWN-REGULATION; TNF-ALPHA; RAW; 264.7; EXPRESSION; REPLICATION; ACTIVATION; ANTIOXIDANT;
D O I
10.7150/ijms.56198
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study examined the effect of the Flos Lonicerae Japonicae water extract (FLJWE), chlorogenic acid, and luteolin on pseudorabies virus (PRV)-induced inflammation in RAW264.7 cells and elucidated related molecular mechanisms. The results revealed that FLJWE and luteolin, but not chlorogenic acid, inhibited the production of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and inflammatory cytokines in PRV-infected RAW 264.7 cells. We found that the FLJWE and luteolin suppressed nuclear factor (NF)-kappa B activation by inhibiting the phosphorylation of signal transducer and activator of transcription 1 and 3 (STAT1 and STAT3, respectively). Moreover, the FLJWE significantly upregulated the expression of pNrf2 and its downstream target gene heme oxygenase-1 (HO-1). Our data indicated that FLJWE and luteolin reduced the expression of proinflammatory mediators and inflammatory cytokines, such as COX-2 and iNOS, through the suppression of the JAK/STAT1/3-dependent NF-kappa B pathway and the induction of HO-1 expression in PRV-infected RAW264.7 cells. The findings indicate that the FLJWE can be used as a potential antiviral agent.
引用
收藏
页码:2285 / 2293
页数:9
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