Effects of total glucosides of paeony on the ulcerative colitis in rats
10.3760/cma.j.issn.1674-635X.2010.04.008
- VernacularTitle:白芍总苷对小鼠溃疡性结肠炎的作用
- Author:
Junying XIANG
;
Qin OUYANG
;
Renwei HU
;
Huatian GAN
- Publication Type:Journal Article
- Keywords:
Ulcerative colitis;
Total glucosides of paeony;
Nuclear factor-κB;
Tumor necrosis factor-α
- From:
Chinese Journal of Clinical Nutrition
2010;18(4):230-234,illust 4
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effects of total glucosides of paeony (TGP) on mice with experimental ulcerative colitis and the underlying mechanisms. Methods Forty-eight mice were equally randomized into 6 groups ( n = 8): normal control group, model group, salicylazosulfapyridine (SASP) group, low-dose TGP group one day after enama, the mice were treated with corresponding agent by oral gavage for3 days. The disease activity index (DAI) score was evaluated every day. After all the mice were scarified, the macroscopic and histological scores were evaluated. The tumor necrosis factor-α (TNF-α) level of the colon mucosa was measured by ELISA and the colonic expression of nuclear factor-κB (NF-κB) p65 was detected by immunohistochemistry. Results Compared with the normal control group, the DAI score was significantly higher in the model group (P ＜0. 01 ),but was similar to that in low-dose TGP group ( P ＞ 0.05 ). Compared with the model group, the DAI score was significantly decreased in SASP group, medium-dose TGP group, and high-dose TGP group (all P ＜ 0. 05). The macroscopic score, histological score, TNF-α level, and expression of NF-κB p65 were significantly higher in model group than in normal control group, SASP group, medium-dose TGP group, and high-dose TGP group ( all P ＜0. 01 ), but was similar to that in low-dose TGP group (P ＞ 0. 05). The efficacy of TGP was higher in high-dose TGP group than in SASP group. Conclusions TGP has certain therapeutic effects on experimental ulcerative colitis,which may be achieved by its inhibitory effect on the activation of NF-κB and the production of TNF-α.
