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甘肃中医药大学,兰州 730000
王凤仪,博士,硕士生导师,教授,从事中医四诊理论研究,E-mail:wfy@gszy.edu.cn
赵党生,硕士生导师,教授,从事中医药治疗肛肠疾病研究,E-mail:zhds69@126.com
收稿日期:2018-12-03,
网络出版日期:2019-05-08,
纸质出版日期:2019-08-20
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王凤仪, 赵党生, 蒲晓薇, 等. 芍药汤对湿热内蕴型溃疡性结肠炎大鼠模型结肠组织中AP-1,TNF-
Feng-yi WANG, Dang-sheng ZHAO, Xiao-wei PU, et al. Effect of Shaoyaotang on Expressions of AP-1 and TNF-
王凤仪, 赵党生, 蒲晓薇, 等. 芍药汤对湿热内蕴型溃疡性结肠炎大鼠模型结肠组织中AP-1,TNF-
Feng-yi WANG, Dang-sheng ZHAO, Xiao-wei PU, et al. Effect of Shaoyaotang on Expressions of AP-1 and TNF-
目的:
2
观察芍药汤对湿热内蕴型溃疡性结肠炎(UC)大鼠模型结肠组织中激活蛋白-1(AP-1)与肿瘤坏死因子-
α
(TNF-
α
)的基因及蛋白表达的影响,探讨芍药汤治疗UC的作用机制。
方法:
2
将60只Wistar大鼠随机分为正常组、模型组、柳氮磺砒啶组及芍药汤低、中、高剂量组,采用病症结合的方法复制湿热内蕴型UC大鼠模型,即高脂高糖辛辣食物及免疫复合法,联合2,4,6-三硝基苯磺酸(TNBS)结合乙醇复合法。造模成功后,分别给予芍药汤低、中、高(6,12,24 g·kg
-1
)灌胃,柳氮磺胺嘧啶1 g·kg
-1
剂量灌胃,正常组给予等体积生理盐水,连续21 d。实时荧光定量聚合酶链式反应(Real-time PCR)检测结肠组织AP-1,TNF-
α
mRNA表达,蛋白免疫印迹法(Western blot)检测结肠组织AP-1,TNF-
α
蛋白表达。
结果:
2
与正常组比较,模型组AP-1,TNF-
α
mRNA及蛋白相对表达量明显升高(
P
<
0.05);与模型组比较,各干预组AP-1,TNF-
α
mRNA及蛋白表达量明显下降(
P
<
0.05),以芍药高剂量组较为明显。
结论:
2
芍药汤可抑制湿热型UC大鼠AP-1蛋白刺激TNF-
α
的表达,可能是其治疗湿热型UC的机制之一。
Objective:
2
To observe the effect of Shaoyaotang on mRNA and protein expressions of colon tissue activated protein-1 (AP-1) and tumor necrosis factor-
α
(TNF-
α
) of hot and humid-type intrinsic ulcerative colitis (UC) model in rats
in order to explore the mechanism of action of herbaceous peony decoction in the treatment of UC.
Method:
2
Totally 60 Wistar rats were randomly divided into blank group
model group
SASP group
and low
medium and high-dose Shaoyaotang groups. The damp-heat intrinsic UC rat model was replicated based on integrated disease and syndrome
namely
high-fat and high-sugar spicy food and immune complex method combined with 2
4
6-trinitrobenzene sulfolnic acid (TNBS) and ethanol complex method. After the successful modeling
low
medium and high-dose Shaoyaotang (6
12
24 g·kg
-1
) was given by gavage
and 1 g·kg
-1
dose of salazol sulfadiazine was given to by gavage. The blank group was given constant volume normal saline for 21 d. Real-time fluorescence quantitative polymerase chain reaction(Real-time PCR) was used to detect mRNA expressions of AP-1 and TNF-
α
in colon tissues
and Western blot was used to detect protein expressions of AP-1 and TNF-
α
in colon tissues.
Result:
2
Compared with the blank group
relative mRNA and protein expressions of AP-1
TNF-
α
in the model group were significantly increased (
P
<
0.05). Compared with the model group
mRNA and protein expressions of AP-1
TNF-
α
in the treatment groups were significantly decreased (
P
<
0.05).
Conclusion:
2
Shaoyaotang can inhibit the expression of TNF-
α
and stimulate AP-1 protein expression in rats with damp-heat UC.
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