Brazilian red propolis effects on peritoneal macrophage activity: Nitric oxide, cell viability, pro-inflammatory cytokines and gene expression

被引:44
作者
Bueno-Silva, Bruno [1 ,2 ]
Kawamoto, Dione [1 ]
Ando-Suguimoto, Ellen S. [1 ]
Casarin, Renato C. V. [5 ]
Alencar, Severino M. [3 ]
Rosalen, Pedro L. [4 ]
Mayer, Marcia P. A. [1 ]
机构
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Microbiol, BR-05508900 Sao Paulo, SP, Brazil
[2] Univ Guarulhos, Dent Res Div, BR-07023070 Guarulhos, SP, Brazil
[3] Univ Sao Paulo, ESALQ, Coll Agr Luiz De Queiroz, BR-13418900 Piracicaba 9, SP, Brazil
[4] Univ Estadual Campinas, Piracicaba Dent Sch, BR-13414903 Piracicaba 52, SP, Brazil
[5] Univ Estadual Campinas, Unicamp, Piracicaba Dent Sch, BR-13414903 Piracicaba, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Natural products; Brazilian red propolis; Inflammation; Macrophage; Cytokines; NF-KAPPA-B; IN-VITRO; NEUTROPHILS MIGRATION; ACTIVATION; KINASE; CARCINOMA; CHEMOKINE; EXTRACT; NEOVESTITOL; MODULATION;
D O I
10.1016/j.jep.2017.06.015
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Propolis has been used in folk medicine since ancient times and it presented inhibitory effect on neutrophil recruitment previously. However, its effect on macrophage obtained from mice remains unclear. Aim of the study: To demonstrate BRP effects on LPS activated peritoneal macrophage. Materials and Methods: Peritoneal macrophages, obtained from C57BL6 mice and activated with LPS, were treated with 50-80 mu g/mL of crude extract of Brazilian red propolis (BRP) during 48 h. Cell viability, levels of NO, 20 cytokines and expression of 360 genes were evaluated. Results: BRP 60 mu g/mL reduced NO production by 65% without affecting the cell viability and decreased production IL1 alpha, IL1 beta, IL4, IL6, IL12p40, Il12p70, IL13, MCP1 and GM-CSF. Molecular mechanism beyond the anti-inflammatory activity may be due to BRP-effects on decreasing expression of Mmp7, Egfr, Adm, Gata3, Wnt2b, Txn1, Herpud1, Axin2, Car9, Id1, Vegfa, Hes1, Hes5, Icam1, Wnt3a, Pcna, Wnt5a, Tnfsf10, Cc15, Il1b, Akt1, Mapk1, Noxa1 and Cdkn1b and increasing expression of Cav1, Wnt6, Calm1, Tnf, Rb1, Socs3 and Dab2. Conclusions: Therefore, BRP has anti-inflammatory effects on macrophage activity by reducing NO levels and diminished release and expression of pro-inflammatory cytokine and genes, respectively.
引用
收藏
页码:100 / 107
页数:8
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