详细信息
当归-红芪超滤膜提取物对糖尿病肾病大鼠肾组织TGF-β_1表达的影响 被引量:22
Effect of Ultra-filtration Extract from Angelice Sinensis Radix and Hedysari Radix on TGF-β_1 in Kidney Tissue of Rat with Diabetic Nephropathy
文献类型:期刊文献
中文题名:当归-红芪超滤膜提取物对糖尿病肾病大鼠肾组织TGF-β_1表达的影响
英文题名:Effect of Ultra-filtration Extract from Angelice Sinensis Radix and Hedysari Radix on TGF-β_1 in Kidney Tissue of Rat with Diabetic Nephropathy
作者:陈张敏[1];李荣科[1];张鹏飞[1];万生芳[1];张凌伟[2];郭钰龙[1];王秋兰[1]
第一作者:陈张敏
机构:[1]甘肃中医药大学,兰州730000;[2]石家庄市妇幼保健院,石家庄050000
第一机构:甘肃中医药大学
年份:2017
卷号:23
期号:5
起止页码:113
中文期刊名:中国实验方剂学杂志
外文期刊名:Chinese Journal of Experimental Traditional Medical Formulae
收录:CSTPCD;;北大核心:【北大核心2014】;CSCD:【CSCD_E2017_2018】;
基金:国家自然科学基金项目(81560718);甘肃省普通本科高等学校基本科研业务费项目[甘财教(2014)63号]
语种:中文
中文关键词:当归-红芪;超滤膜提取物;糖尿病肾病;转化生长因子-β1;Smad2/3
外文关键词:transforming growth Angelice Sinensis Radix-Hedysari Radix; ultra-filtration extract; diabetic nephropathy; factor-β1 ; Smad2/3
摘要:目的:研究当归-红芪超滤膜提取物对糖尿病肾病(DN)大鼠肾组织转化生长因子-β_1(TGF-β_1),Smad信号通路的调控作用,探讨其对DN大鼠的作用及产生该作用可能的机制。方法:采用一次性大剂量(60 mg·kg-1)腹腔注射链脲佐菌素(STZ)诱导建立DN大鼠模型。将DN大鼠随机分为正常组、模型组、厄贝沙坦组及当归-红芪超滤膜提取物低、中、高剂量组,之后开始灌胃给药,每天1次,8周后测空腹血糖(FBG),尿素氮(BUN),血肌酐(SCr),24 h尿蛋白;光镜观察肾组织结构变化;酶联免疫吸附测定(ELISA)检测大鼠TGF-β_1,Smad2/3含量;免疫组化法检测肾组织TGF-β_1,Smad2/3蛋白的表达;实时荧光定量聚合酶链式反应(Real-time PCR)法检测肾组织TGF-β_1,Smad2/3的mRNA表达。结果:与正常组比较,模型组大鼠FBG,BUN,SCr,24 h尿蛋白水平明显升高,ELISA检测大鼠TGF-β_1,Smad2/3含量明显升高,肾组织病理结构异常较为明显,TGF-β_1,Smad2/3蛋白量表达明显升高(P<0.05,P<0.01);与模型组比较,当归-红芪超滤膜提取物各组均不同程度降低了DN大鼠FBG,BUN,SCr,24 h尿蛋白水平(P<0.05);ELISA检测大鼠TGF-β_1,Smad2/3含量降低(P<0.05),肾组织病理结构异常得到改善,TGF-β_1,Smad2/3蛋白量表达减少(P<0.05,P<0.01),TGF-β_1,Smad2/3 mRNA表达减少(P<0.05,P<0.01)。结论:当归-红芪超滤膜提取物可改善DN大鼠肾功能病变,延缓DN慢性病理进展,其机制可能与其抑制TGF-β_1/Smad信号通路有关。
Objective: To study the regulatory effect of ultra-filtration extract from Angelice Sinensis Radix and Hedysari Radix (UFEASH) on transforming growth factor-β1(TGF-β1) and Smad signaling pathway of kidney tissue of rat with diabetic nephropathy (DN) , and explore its possible mechanism. Method : The rat model with DN was induced by one-time high-dose (60 mg·kg^-1) intraperitoneal injection with streptozotocin (STZ). All experimental rats were divided into blank group, model group, irbesartan group and low, median, high-dose UFEASH groups, and then intragastrieally administrated once a day. Fasting blood glucose, urea nitrogen (BUN) ,serum creatinine (SCr) , 24 h urinary protein were detected after 8 weeks. The changes in renal tissue structure were observed under light microscope. TGF-β1 and smad2/3 content of the rats were tested by ELISA. The expression of TGF-β1, Smad2/3 protein and mRNA expressions in renal tissues were detected by immunohistochemistry and Real-time PCR, respectively. Result: Compared with the normal group, the model group showed significant increases in FBG, BUN, SCr and 24 h urinary protein; ELISA showed notable increases in TGF-/31 and Smad2/3 content, remarkable renal pathological structural abnormality and notable increase in TGF- 131 and Smad2/3 protein expressions (P 〈 0.05, P 〈 0.01 ). Compared with the model group, UFEASH groups significantly reduced the level of FBG, BUN, SCr and 24 h urine protein of rats with DN (P 〈 0.05 ). The levels of TGF-β1 and Smad2/3 mRNA expressions were also decreased (P 〈 0.05 ). The abnormal structure of renal tissue was alleviated. The expression of TGF-β1 and Smad2/3 were reduced (P 〈 0.05, P 〈 0.01 ). Conclusion: UFEASH can improve renal function in rats with DN and delay the chronic pathological progress of DN, which may be related to the inhibition of TGF-β1/Smad signaling pathway.
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