Portulaca Extract Attenuates Development of Dextran Sulfate Sodium Induced Colitis in Mice through Activation of PPARγ.
Rui KongHui LuoNan WangJingjing LiShizan XuKan ChenJiao FengLiwei WuSainan LiTong LiuXiya LuYujing XiaYanhong ShiYingqun ZhouWeigang HeQi DaiYue-Juan ZhengJie LuPublished in: PPAR research (2018)
Portulaca oleracea L. is a traditional Chinese medicine, which has been used as adjuvant therapy for inflammatory bowel disease (IBD). However, the mechanism of its activity in IBD still remains unclear. Since previous studies have documented the anti-inflammatory effect of peroxisome proliferator activated receptors-γ (PPAR-γ), Portulaca regulation of PPAR-γ in inflammation was examined in current study. Ulcerative colitis (UC) was generated by 5% dextran sulfate sodium (DSS) in mice and four groups were established as normal control, DSS alone, DSS plus mesalamine, and DSS plus Portulaca. Severity of UC was evaluated by body weight, stool blood form, and length of colorectum. Inflammation was examined by determination of inflammatory cytokines (TNF-a, IL-6, and IL-1a). Portulaca extract was able to attenuate development of UC in DSS model similar to the treatment of mesalazine. Moreover, Portulaca extract inhibited proinflammatory cytokines release and reduced the level of DSS-induced NF-κB phosphorylation. Furthermore, Portulaca extract restored PPAR-γ level, which was reduced by DSS. In addition, Portulaca extract protected DSS induced apoptosis in mice. In conclusion, Portulaca extract can alleviate colitis in mice through regulation of inflammatory reaction, apoptosis, and PPAR-γ level; therefore, Portulaca extract can be a potential candidate for the treatment of IBD.
Keyphrases
- oxidative stress
- induced apoptosis
- anti inflammatory
- ulcerative colitis
- diabetic rats
- insulin resistance
- body weight
- high fat diet induced
- endoplasmic reticulum stress
- signaling pathway
- metabolic syndrome
- type diabetes
- skeletal muscle
- early stage
- nuclear factor
- high resolution
- wild type
- toll like receptor
- drug induced
- stress induced
- pi k akt
- liquid chromatography