Anti-inflammatory potential of pyocyanin in LPS-stimulated murine macrophages

被引:9
|
作者
de Sales-Neto, Jose Marreiro [1 ]
Lima, E. A. [1 ]
Cavalcante-Silva, L. H. A. [1 ]
Vasconcelos, U. [2 ]
Rodrigues-Mascarenhas, S. [1 ]
机构
[1] Univ Fed Paraiba, Dept Biol Celular & Mol, Joao Pessoa, Paraiba, Brazil
[2] Univ Fed Paraiba, Dept Biotecnol, Joao Pessoa, Paraiba, Brazil
关键词
Inflammation; natural phenazines; Pseudomonas aeruginosa; macrophages; immune response; TUMOR-NECROSIS-FACTOR; PSEUDOMONAS-AERUGINOSA; NITRIC-OXIDE; MAST-CELLS; INDUCED TOXICITY; VASCULAR-PERMEABILITY; NEUTROPHIL APOPTOSIS; 1321N1; ASTROCYTOMA; LUNG; INFLAMMATION;
D O I
10.1080/08923973.2018.1555845
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Context: Pyocyanin is a typical Pseudomonas aeruginosa virulence factor, a common Gram-negative rod responsible for a wide range of severe nosocomial infections. There is evidence indicating that pyocyanin has multiple biological activities, but little is known about anti-inflammatory properties.Objective: This study investigated pyocyanin effect on nitric oxide and cytokine production in lipopolysaccharide (LPS)-activated murine peritoneal macrophages.Materials and methods: Macrophages were incubated in the presence and absence of pyocyanin (1, 5, 10, 50, and 100 mu M) with and without LPS (1 mu g/mL). Nitric oxide production was determined by Griess reagent and tumor necrosis factor (TNF)- and interleukin (IL)-1 production was assessed by enzyme-linked immunosorbent assay. In addition, pyocyanin effects on zymosan A-induced peritonitis in mice were evaluated.Results: Pyocyanin (5 and 10 mu M) decreased nitric oxide, TNF-, and IL-1 production independent of macrophage death. On the other hand, in vivo, pyocyanin (5 mg/kg) was not able to affect leukocyte migration into the site of inflammation.Discussion and conclusion: Thus, our findings suggest that pyocyanin exerts anti-inflammatory effects on murine peritoneal macrophages, downregulating nitric oxide, TNF-, and IL-1 levels, which seems to be independent of cell migration. These effects may represent a mechanism of immune evasion; nevertheless more detailed studies should be performed to confirm this hypothesis.
引用
收藏
页码:102 / 108
页数:7
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