Department of Clinical and Experimental Medicine and Pharmacology, School of Medicine, University of Messina, 98123 Messina, Italy.
PPAR Res. 2010;2010:917312. doi: 10.1155/2010/917312. Epub 2010 Jun 30.
The previous results suggest that peroxisome proliferator-activated receptor-alpha (PPAR)-alpha, an intracellular transcription factor activated by fatty acids, plays a role in control of inflammation. There is persuasive epidemiological and experimental evidence that dietary polyphenols have anti-inflammatory activity. In this regard, it has been demonstrated that verbascoside (VB) functions as intracellular radical scavenger and reduces the microscopic and macroscopic signs of experimental colitis. With the aim to characterize the role of PPAR-alpha in VB-mediated anti-inflammatory activity, we tested the efficacy of VB in an experimental model of inflammatory bowel disease induced by dinitrobenzene sulfonic acid, comparing mice lacking PPAR-alpha (PPAR-alphaKO) with wild type (WT) mice. Results indicate that VB-mediated anti-inflammatory activity is weakened in PPAR-alphaKO mice, compared to WT controls, especially in the inhibition of neutrophil infiltration, intestinal permeability and colon injury. These results indicate that PPAR-alpha can contribute to the anti-inflammatory activity of VB in inflammatory bowel disease.
先前的研究结果表明,过氧化物酶体增殖物激活受体-α(PPAR-α)是一种被脂肪酸激活的细胞内转录因子,在炎症控制中发挥作用。有充分的流行病学和实验证据表明,膳食多酚具有抗炎活性。在这方面,已经证明毛蕊花糖苷(VB)作为细胞内自由基清除剂,可减少实验性结肠炎的微观和宏观迹象。为了表征 PPAR-α在 VB 介导的抗炎活性中的作用,我们在二硝基苯磺酸诱导的实验性肠炎模型中测试了 VB 的功效,将缺乏 PPAR-α 的小鼠(PPAR-αKO)与野生型(WT)小鼠进行比较。结果表明,与 WT 对照组相比,VB 介导的抗炎活性在 PPAR-αKO 小鼠中减弱,特别是在抑制中性粒细胞浸润、肠通透性和结肠损伤方面。这些结果表明,PPAR-α可以促进 VB 在炎症性肠病中的抗炎活性。