Mogroside V exerts anti-inflammatory effects on fine particulate matter-induced inflammation in porcine alveolar macrophages

被引:19
作者
Shen, Jiakun [1 ,2 ]
Shen, Dan [1 ,2 ]
Tang, Qian [1 ,2 ]
Li, Zhaojian [1 ,2 ]
Jin, Xiaoming [1 ,2 ]
Li, Chunmei [1 ,2 ]
机构
[1] Nanjing Agr Univ, Coll Anim Sci & Technol, Res Ctr Livestock Environm Control & Smart Prod, 1 Weigang, Nanjing 210095, Jiangsu, Peoples R China
[2] Nanjing Agr Univ, Natl Ctr Int Res Anim Gut Nutr, Nanjing, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Mogroside V; Porcine alveolar macrophages; Inflammation; PM2.5; NITRIC-OXIDE PRODUCTION; IN-VITRO; NLRP3; INFLAMMASOME; OXIDATIVE STRESS; ACTIVATION; POLARIZATION; EXPRESSION; INHIBITORS; INDUCTION; PATHWAY;
D O I
10.1016/j.tiv.2022.105326
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Mogroside V is the main bioactive component of Siraitia grosvenorii (Swingle), and has a potential anti-inflammatory function. However, the effect of mogroside V on fine particulate matter (PM2.5)-induced inflammation has not been reported. In the present study, the biological effect of mogroside V on inflammation was investigated in PM2.5- treated porcine alveolar macrophages (3D4/21). The results showed that mogroside V significantly inhibited PM2.5-induced nitric oxide (NO) production and rescued the arginase activity inhibited by PM2.5. In the presence of mogroside V, the upregulation of IL-18, TNF-alpha and COX-2 by PM2.5 in 3D4/21 cells was inhibited. Mogroside V attenuated PM2.5-induced phosphorylation of NF-kappa B p65 and the expression of NLRP3. Mogroside V reduced intracellular ROS levels induced by PM2.5. In the transcriptomic analysis, inflammation-related genes in 3D4/21 cells were not significantly affected after treatment with mogroside V. These results indicated that mogroside V can alleviate the inflammatory response of porcine alveolar macrophages induced by PM2.5 from pig house and that mogroside V may play the role through the antioxidant function of eliminating ROS. Mogroside V has a clear anti-inflammatory function in the presence of inflammation.
引用
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页数:9
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