Yunusi Kurexi, Zhang Jingping, Zhong Li, Mosha Gulinisha, Nuermaimaiti Ajiguli, Abudula Mairipaiti, Upur Halmurat
Department of Molecular Biology and Biochemistry, College of Basic Medicine, Xinjiang Medical University, Urumqi, Xinjiang, 830000, China.
Traditional Uighur Medicine Institute, Xinjiang Medical University, Urumqi, Xinjiang, 830000, China.
BMC Complement Altern Med. 2015 May 22;15:152. doi: 10.1186/s12906-015-0672-x.
The aim of this study was to investigate the mechanisms underlying the therapeutic effect of Uygur medicine KJA on UC in a rat model.
UC was induced in Wistar rats by application of 2, 4-dinitrochlorobenzene and acetic acid and were then treated with three different doses of KJA, and normal saline as control. After treatment for 20 days, the gene expression profile of colonic tissue was analyzed by microarray and verified by quantitative real-time RT-PCR.
Animals treated with the three different doses of KJA were compared with normal saline controls, wherein microarray analysis identified 1991, 2163, and 1677 differentially expressed genes respectively, of which 444 genes were raised and 670 genes were decrease spliced together in the three doses tested. The KEGG pathway analyses found commonly raised genes related to several different biological functions. Interesting genes included TRL2, IL-1β, TGF-β1, and NF-κB were confirmed by quantitative PCR.
The therapeutic effect of KJA on UC is likely explained by specific effects on the expression of genes, which are the effector molecules known to be involved in the development of UC. Further studies on differentially expressed genes will help explain the mechanism of action of Uygur medicine KJA.
本研究旨在探讨维吾尔药KJA对大鼠溃疡性结肠炎(UC)治疗作用的潜在机制。
通过应用2,4-二硝基氯苯和乙酸诱导Wistar大鼠患UC,然后用三种不同剂量的KJA进行治疗,并以生理盐水作为对照。治疗20天后,通过基因芯片分析结肠组织的基因表达谱,并通过定量实时RT-PCR进行验证。
将用三种不同剂量KJA治疗的动物与生理盐水对照组进行比较,其中基因芯片分析分别鉴定出1991、2163和1677个差异表达基因,在测试的三种剂量中,共有444个基因上调,670个基因剪接减少。KEGG通路分析发现常见的上调基因与几种不同的生物学功能相关。通过定量PCR证实了包括TRL2、IL-1β、TGF-β1和NF-κB在内的有趣基因。
KJA对UC的治疗作用可能是通过对基因表达的特定影响来解释的,这些基因是已知参与UC发病的效应分子。对差异表达基因的进一步研究将有助于解释维吾尔药KJA的作用机制。