银屑I号对咪喹莫特诱导小鼠银屑病模型核转录因子-κB的调控作用及机制  被引量:9

Effects of Yinxieyihao on Nuclear Factor Kappa B for Imiquimod Induced Psoriasis Mice Model

在线阅读下载全文

作  者:孙文[1] 陈雨佳[1] 邓婉莹[1] 黄树宏[1] 李勇[2] 刘靖[2] 查旭山[2] SUN Wen CHEN Yu-jia DENG Wan-ying HUANG Shu-hong LI Yong LIU Jing CHA Xu-shan(Guangzhou University of Traditional Chinese Medicine, Guangzhou 510405, China The first affiliated hospital of guan- gzhou university of TCM , Guangzhou 510405, China)

机构地区:[1]广州中医药大学,广东广州510405 [2]广州中医药大学第一附属医院,广东广州510405

出  处:《中国皮肤性病学杂志》2017年第1期79-81,94,共4页The Chinese Journal of Dermatovenereology

基  金:国家自然科学基金面上项目(81573980);国家自然科学基金青年项目(81202699)

摘  要:目的观察银屑I号对咪喹莫特(imiquimod,IMQ)诱导小鼠银屑病模型核转录因子-κB(nuclear factor,NF-κB)炎症通路的影响及其可能的作用机制。方法建立IMQ诱导小鼠银屑病模型,随机分为模型组、银屑I号组、雷公藤多甙组,每组10只,另选正常小鼠10只作为空白对照组,空白对照组及模型组予等量生理盐水灌胃,银屑I号组、雷公藤多甙组分别给予银屑I号、雷公藤多甙灌胃,连续10天,HE染色观察各组小鼠皮损组织形态学变化;免疫组化法检测皮损组织NF-κB p65蛋白水平,RT-PCR法检测NF-κB mRNA表达情况,订制血液蛋白芯片检测血清白介素6(interleukin 6,IL-6)、白介素10(interleukin 10,IL-10)、白介素17(interleukin 17,IL-17)、干扰素γ(interferon gamma,INF-g)含量。结果与空白对照组比较,模型组小鼠出现明显的红斑、鳞屑及皮肤增厚。与模型组比较,银屑I号组、雷公藤多甙组小鼠红斑、鳞屑及皮肤增厚程度明显减轻;银屑I号组、雷公藤多甙组血清IL-6、IL-10、IL-17、INF-γ水平明显降低(P均<0.01);银屑I号组、雷公藤多甙组皮损组织NF-κB mRNA、NF-κB p65表达也明显降低(P均<0.01)。结论银屑I号能够明显抑制IMQ诱导小鼠模型皮肤增殖,这可能与抑制NF-κB基因表达及减轻炎症反应有关。Objective To observe the effects of YinXieYiHao (YXIH) on nuclear factor (NF) kappa B inflammatory pathway for imiquimod ( IMQ ) induced psoriasis mice model and analysis it' s possible therapeutic rneehanism. Methods IMQ induced psoriasis mice mode/were conducted,which were randomly divided into model group( MP), YXIH group(YXYHP) , tripterygium glycosides group( TGP), another 10 mice were divided into blank control group(BCP). Corresponding lavage method were employed for teen days. RT-PCR and IHC were applied to deteete protein and gene expression level of NF-κB in mice skin issue. HE staining were em ployed to observe the histological changes of mice skin issue. We detected IL-6, IL-10, IL-17, INF-g level of peripheral blood. Results MP appeared obvious erythema, scales and thickening of the skin; Compared with BCP, erythema, scales and skin thickened of other groups were significantly reduce; Compared with MP, IL-6, IL-10, 1L-17,INF-g level of peripheral blood were significantly decreased in YXYHP,TGP (all P 〈 0.01 ). Compared with MP, expression of NF-κBmRNA in YXYHP,TGP were obviously declined ( all P 〈 0.01 ), so was the expression of NF-KB p65. Conclusion YXIH could reduce inflammatory response of psoriasis mice model, the mechanism of which may be associated with the inhibition of NF-κB expression.

关 键 词:银屑I号 NF-ΚB 小鼠 咪喹莫特 干扰素 白介素 

分 类 号:R758.63[医药卫生—皮肤病学与性病学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象