中国药物与临床
中國藥物與臨床
중국약물여림상
CHINESE REMEDIES & CLINICS
2014年
6期
736-738
,共3页
刘其锋%郁丽霞%李莎莎%顾晓霞%叶建明
劉其鋒%鬱麗霞%李莎莎%顧曉霞%葉建明
류기봉%욱려하%리사사%고효하%협건명
人参皂甙类%环孢菌素%转化生长因子β%α平滑肌肌动蛋白%钙黏着糖蛋白类
人參皂甙類%環孢菌素%轉化生長因子β%α平滑肌肌動蛋白%鈣黏著糖蛋白類
인삼조대류%배포균소%전화생장인자β%α평활기기동단백%개점착당단백류
Ginsenosides%Cyclosporine%Transforming growth factor-beta%Alpha-smooth muscle actin%Cadherins
目的:探讨人参皂苷Rg1(G-Rg1)对环孢素A(CsA)慢性肾毒性大鼠肾脏肾小管上皮-间充质细胞转分化(EMT)的抑制作用。方法雄性SD大鼠24只,随机分为3组:正常组、模型组、G-Rg1干预组,采用低盐饮食加CsA灌胃的方法建立CsA慢性肾纤维化模型,CsA剂量为25 mg·kg-1·d-1。观察G-Rg1对大鼠尿量、肾功能、肾脏病理及肾脏转化生长因子(TGF)-β1、E-钙黏素、α-平滑肌肌动蛋白(SMA)表达的影响。结果 G-Rg1能抑制CsA慢性肾毒性大鼠肾脏纤维化,下调TGF-β1、α-SMA在肾组织的表达,同时上调肾组织E-钙黏素的表达。结论 G-Rg1对CsA慢性肾毒性大鼠具有保护作用,其机制可能是抑制了肾组织的EMT途径。
目的:探討人參皂苷Rg1(G-Rg1)對環孢素A(CsA)慢性腎毒性大鼠腎髒腎小管上皮-間充質細胞轉分化(EMT)的抑製作用。方法雄性SD大鼠24隻,隨機分為3組:正常組、模型組、G-Rg1榦預組,採用低鹽飲食加CsA灌胃的方法建立CsA慢性腎纖維化模型,CsA劑量為25 mg·kg-1·d-1。觀察G-Rg1對大鼠尿量、腎功能、腎髒病理及腎髒轉化生長因子(TGF)-β1、E-鈣黏素、α-平滑肌肌動蛋白(SMA)錶達的影響。結果 G-Rg1能抑製CsA慢性腎毒性大鼠腎髒纖維化,下調TGF-β1、α-SMA在腎組織的錶達,同時上調腎組織E-鈣黏素的錶達。結論 G-Rg1對CsA慢性腎毒性大鼠具有保護作用,其機製可能是抑製瞭腎組織的EMT途徑。
목적:탐토인삼조감Rg1(G-Rg1)대배포소A(CsA)만성신독성대서신장신소관상피-간충질세포전분화(EMT)적억제작용。방법웅성SD대서24지,수궤분위3조:정상조、모형조、G-Rg1간예조,채용저염음식가CsA관위적방법건립CsA만성신섬유화모형,CsA제량위25 mg·kg-1·d-1。관찰G-Rg1대대서뇨량、신공능、신장병리급신장전화생장인자(TGF)-β1、E-개점소、α-평활기기동단백(SMA)표체적영향。결과 G-Rg1능억제CsA만성신독성대서신장섬유화,하조TGF-β1、α-SMA재신조직적표체,동시상조신조직E-개점소적표체。결론 G-Rg1대CsA만성신독성대서구유보호작용,기궤제가능시억제료신조직적EMT도경。
Objective To investigate the effects of ginsenoside Rg1 (G-Rg1) on renal epithelial-mesenchymal transformation (EMT) in rats with chronic cyclosporine A (CsA) nephrotoxicity. Methods Twenty-four male SD rats were randomly assigned to normal control group, model control group and G-Rg1 treatment group. Low-salt diet and CsA were administered by gastric injection at the dose of 25 mg·kg-1·d-1 for establishing the models of chronic CsA nephrotoxicity. The effects of G-Rg1 on the volume of urine, renal function, renal pathophysioiogy and renal TGF-β1, E-cadherin and α-SMA expressions were determined. Results G-Rg1 down-regulated TGF-β1 and α-SMA and up-regulated E-cadherin expressions in renal tissues in rats with chronic CsA nephmtoxicity. Conclusion G-Rg1 harbors protective effects to the kidneys in rats possibly via inhibition of the EMT process.