Colonic macrophage-targeted curcumin nanoparticles alleviate DSS-induced colitis in mice through the NF-kappa B pathway

被引:8
作者
Liu, Gaodan [1 ,2 ]
Feng, Simin [1 ,2 ]
Sun, Yuxin [1 ,2 ]
Wang, Dan [1 ,2 ]
Shao, Ping [1 ,2 ]
Sun, Peilong [1 ,2 ]
机构
[1] Zhejiang Univ Technol, Dept Food Sci & Engn, Hangzhou 310014, Zhejiang, Peoples R China
[2] Zhejiang Univ Technol, China Natl Light Ind, Key Lab Food Macromol Resources Proc Technol, Hangzhou, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Nanoparticles; Ulcerative colitis; Macrophage-targeted; Curcumin; Oral administration; LOADED ZEIN NANOPARTICLES; SODIUM-INDUCED COLITIS; ANTISOLVENT PRECIPITATION; ULCERATIVE-COLITIS; ENCAPSULATION; FABRICATION; BIOACCESSIBILITY; POLYSACCHARIDE; NANOMATERIALS; SOLUBILITY;
D O I
10.1016/j.fbio.2021.101089
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Oral targeted anti-inflammatory bioactive compounds released in the intestine to relieve the symptoms of ulcerative colitis have bacame a research hot spot. In this study, we investigated the colitis preventive effect of macrophage-targeted curcumin (Cur), which is encapsulated in chondroitin sulfate (CS) and zein (Z) based nanoparticles (NP). In vitro simulated digestion experiments revealed that Cur/CS/Z NP was more stable than Cur/Tre/Z NP (Cur/tremella polysaccharide/Z NP). Cytotoxicity, macrophage-targeting and colitis inhibiting effects of NP were investigated in both Raw 264.7 cells in vitro and DSS-induced colitis animal model in vivo. Compared with Cur/Tre/Z NP, Cur/CS/Z NP had stronger macrophage targeting effects. Both Cur/Z NP and Cur/ CS/Z NP significantly ameliorated the symptoms of colitis by inhibiting the expression of COX-2, TNF-alpha, CSF-1, IL-1 beta and IL-6 through NF-kappa B pathway, while Cur/Z NP was less effective. These findings revealed that CS, as a targeted ligand of curcumin nanoparticles, enabled Cur/CS/Z NP to reach the colon and alleviated DSS-induced colitis in mice by inhibiting NF-kappa B activity.
引用
收藏
页数:12
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