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作 者:黄亦彤[1] 钟志勇[2] 吕永慧[1] 武昕[2] 潘竞锵[1] 蓝天美 严家荣[2] HUANG Yi-tong ZHONG Zhi-yong LV Yong-hui WU Xin PAN J ing-qiang LAN Tian-mei YAN J ia-rong(Department of Pharmaceutical, The Chinese Medicine Hospital in Guangzhou, Guangzhou 510000, China Medical Experimental Animal Center of Guangdong Province, Guangzhou 510000, China)
机构地区:[1]广州市中医医院药学部,广东广州510000 [2]广东省医学实验动物中心,广东广州510000
出 处:《中国中西医结合消化杂志》2016年第12期906-910,915,共6页Chinese Journal of Integrated Traditional and Western Medicine on Digestion
基 金:广州市医药卫生科技项目中医药科技项目(No:20132A011012)
摘 要:[目的]观察肠炎清对免疫复合溃疡型结肠炎模型(ICUC)大鼠结肠组织核因子-κB(NF-κB)蛋白表达及Toll样受体4(TLR4)、髓样分化因子88(MyD88)基因表达的影响,探讨其治疗IBD的作用机制。[方法]采用三硝基苯磺酸(TNBS)加免疫复合法造模。将大鼠随机分为空白对照组、模型对照组、肠炎清低、中、高剂量组(8.33、16.67、33.33ml/kg)、柳氮磺吡啶(SASP)组(0.5g/kg)。造模后第2天,用药组分别给予相应药物灌胃,7d后,麻醉处死大鼠,取新鲜结肠标本。采用免疫组化法检测NF-κBp65的蛋白表达,实时定量PCR法(qRT-PCR)检测TLR4mRNA、MyD88mRNA的表达。[结果]免疫组化结果 NF-κBp65在各组各只动物均可见阳性表达,其中肠炎清高剂量组及SASP组可显著下调NF-κBp65的表达,差异有统计学意义(P<0.05)。PCR结果:造模后动物结肠组织TLR4mRNA、MyD88mRNA的表达量均有升高。与模型对照组比较,各给药组TLR4 mRNA、MyD88mRNA表达均有不同程度的下调,但差异无统计学意义。[结论]肠炎清能下调NF-κBp65蛋白表达、TLR4、MyD88基因表达,其作用机制可能与调控TLR4/MyD88/NF-κB信号转导通路有关。[Objective]To observe the expression of NF-κB and the expression of TLR4 and MyD88gene in colonic tissue of rats with immune complex ulcerative colitis(ICUC)And explore the mechanism of IBD treatment.[Methods]Trinitrobenzene sulfonic acid(TNBS)plus immune complex method were used to make the rats modle which were randomly divided into blank control group,model control group,enteritis of low,medium and high dose group(8.33,16.67,33.33ml/kg),willow nitrogen sulfonyl pyridine(SASP)group(0.5g/kg).After 2days,The treatment group rats were sacrificed after administrating the corresponding drugs for 7days,and fresh colon specimens were taken.The protein expression of NF-κBp65was detected by immunohistochemical method and the expression of TLR4 mRNA and MyD88 mRNA was detected by RT-PCR.[Results]Immunohistochemical results:The nf-kappa Bp65 positive expression,appear in both groups of various animals including enteritis lofty dose group and SASP group significantly lowered the nf-kappa Bp65 expression,statistically significant(P〈0.05).The PCR results:The expressions of TLR4 mRNA and MyD88 mRNA in the colon tissue of the animals were increased after modeling.Compared with model control group,TLR4 mRNA and MyD88 mRNA expression were down-regulated in different dose groups,but there was no significant difference.[Conclusion]Changyanqing decoction can decrease the expression of nf-kappa Bp65 protein and the TLR4,MyD88 gene.Its mechanism may be related to the regulation of-TLR4/MyD88/nf-kappa B signal transduction pathway.
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