Effects of mimic of manganese superoxide dismutase on 2,4,6-trinitrobenzene sulfonic acid-induced colitis in rats

被引:10
作者
Wang, Yan-Hong [1 ]
Dong, Jiao [2 ]
Zhang, Jian-Xin [1 ]
Zhai, Jing [1 ]
Ge, Bin [1 ]
机构
[1] Gansu Prov Hosp, Dept Pharm, 204 Donggangxi Rd, Lanzhou 730000, Gansu, Peoples R China
[2] Cent Mil Commiss, Outpatient Dept Xiaoxitian, Hosp Chinese PLA 309, Agcy Off Adm, Beijing 100082, Peoples R China
关键词
Mimic of manganese superoxide dismutase; 2,4,6-trinitrobenzenesulfonic acid; Colitis; Anti-inflammatory; TLR4; Nuclear factor-kappa B; INFLAMMATORY-BOWEL-DISEASE; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; INDUCED ULCERATIVE-COLITIS; FACTOR-ALPHA; EPITHELIAL-CELLS; RESVERATROL; APOPTOSIS; MICE; CHONDROCYTES;
D O I
10.1007/s12272-016-0811-z
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The mimic of manganese superoxide dismutase (MnSODm) has been synthesized and reported to have anti-inflammatory properties. However, whether MnSODm has anti-inflammatory effects on colitis and any underlying mechanisms are poorly understood. This study was to investigate therapeutic effects and mechanism of MnSODm on 2,4,6-trinitrobenzenesulfonic acid (TNBS) induced colitis model in rats. Rats were intragastrically administered MnSODm (10, 20, and 40 mg/kg) per day for 7 days after colitis was induced by TNBS. After treated with MnSODm, the colonic macroscopic and microscopic damage scores and colonic weight/length ratios were significantly decreased compared with colitis model group. Myeloperoxidase (MPO) activity, malonyldialdehyde (MDA), tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1 beta, IL-6, and IL-8 levels in colon tissues were also significantly decreased in MnSODm treatment groups. However, superoxide dismutase (SOD) activity significantly increased and phosphorylated inhibitory kappa B-alpha (I kappa B alpha), inhibitor kappa B kinase (IKK alpha/beta), and nuclear factor-kappa Bp65 (NF-kappa Bp65) as well as Toll-like receptor 4 (TLR4) and myeloid differentiation actor 88 (MyD88) in the colonic mucosa were significantly inhibited by MnSODm treatment. Thus, MnSODm was protective against colitis via antioxidant activity and by inhibiting inflammatory mediators by down-regulating TLR4/MyD88/NF-kappa B signaling pathways. These data suggest a potential therapeutic effect of MnSODm in colitis.
引用
收藏
页码:1296 / 1306
页数:11
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