中国中西医结合肾病杂志
中國中西醫結閤腎病雜誌
중국중서의결합신병잡지
CHINESE JOURNAL OF INTEGRATED TRADITIONAL AND WESTERN NEPHROLOGY
2014年
5期
381-384
,共4页
周瑾%陈香美%魏日胞%刘述文%丁瑞%刘航%傅博
週瑾%陳香美%魏日胞%劉述文%丁瑞%劉航%傅博
주근%진향미%위일포%류술문%정서%류항%부박
肾间质成纤维细胞%复方鳖甲软肝片方%血清药理学%FN%ColⅠ%ColⅢ
腎間質成纖維細胞%複方鱉甲軟肝片方%血清藥理學%FN%ColⅠ%ColⅢ
신간질성섬유세포%복방별갑연간편방%혈청약이학%FN%ColⅠ%ColⅢ
Renal interstitional fibroblast%CBRP%Serological pharmacology%Fibronectin%CollagenⅠ%Collagen Ⅲ
目的:观察中药“复方鳖甲软肝片方”对TGF-β1诱导的肾间质成纤维细胞(NRK-49F)增殖及分泌细胞外基质的影响。方法:以2 ng/ml hTGF -β1诱导 NRK -49F 细胞,并以软肝片方大、中、小剂量(分别以7g/kg、3.5 g/kg、1.75 g/kg)药物血清进行干预,分别应用MTT法、ELISA、免疫细胞化学方法,观察肾间质成纤维细胞增殖、细胞上清FN浓度及ColⅠ、ColⅢ的表达。结果:软肝方含药血清对hTGF-β1诱导的细胞增殖无影响;但大、中剂量软肝方能不同程度地降低FN的分泌及ColⅠ、ColⅢ的表达,软肝方大剂量组作用最强(P<0.01)。结论:复方鳖甲软肝片方在一定程度上抑制TGF-β1诱导的肾间质成纤维细胞ColⅠ或ColⅢ的表达,大剂量软肝方作用最强。
目的:觀察中藥“複方鱉甲軟肝片方”對TGF-β1誘導的腎間質成纖維細胞(NRK-49F)增殖及分泌細胞外基質的影響。方法:以2 ng/ml hTGF -β1誘導 NRK -49F 細胞,併以軟肝片方大、中、小劑量(分彆以7g/kg、3.5 g/kg、1.75 g/kg)藥物血清進行榦預,分彆應用MTT法、ELISA、免疫細胞化學方法,觀察腎間質成纖維細胞增殖、細胞上清FN濃度及ColⅠ、ColⅢ的錶達。結果:軟肝方含藥血清對hTGF-β1誘導的細胞增殖無影響;但大、中劑量軟肝方能不同程度地降低FN的分泌及ColⅠ、ColⅢ的錶達,軟肝方大劑量組作用最彊(P<0.01)。結論:複方鱉甲軟肝片方在一定程度上抑製TGF-β1誘導的腎間質成纖維細胞ColⅠ或ColⅢ的錶達,大劑量軟肝方作用最彊。
목적:관찰중약“복방별갑연간편방”대TGF-β1유도적신간질성섬유세포(NRK-49F)증식급분비세포외기질적영향。방법:이2 ng/ml hTGF -β1유도 NRK -49F 세포,병이연간편방대、중、소제량(분별이7g/kg、3.5 g/kg、1.75 g/kg)약물혈청진행간예,분별응용MTT법、ELISA、면역세포화학방법,관찰신간질성섬유세포증식、세포상청FN농도급ColⅠ、ColⅢ적표체。결과:연간방함약혈청대hTGF-β1유도적세포증식무영향;단대、중제량연간방능불동정도지강저FN적분비급ColⅠ、ColⅢ적표체,연간방대제량조작용최강(P<0.01)。결론:복방별갑연간편방재일정정도상억제TGF-β1유도적신간질성섬유세포ColⅠ혹ColⅢ적표체,대제량연간방작용최강。
Objective:Objective:in vitro,we object the effect of Compound Biejia Ruangan Precription( CBRP) on renal in-terstitial fibroblast proliferation and excreting extracellular matrix induced by TGF-β1 . Methods:Using method of serological pharma-cology, rat renal interstitial fibroblast (NRK-49F cell) stimulated with TGF-β1, simultaneously 10% different rat serum was add-ed to for 48 h as follows:the normal rat serum( male SD rats were given physiological saline by gastric gavages) , the low dose CBRP-medicated rat serum (given CBRP 7 g/kg), the middling dose one(given CBRP 3. 5 g/kg), the high dose one(given CBRP 1. 75 g/kg), applying to immunocytochemistry, MTT assay, ELISA, cell proliferation and extracellular matrix such as fibronectin, typeⅠcollagen, typeⅢ collagen were detected. Results:Contrasted with the normal rat serum: rat serum medicated-CBRP had no effect on NRK-49F cell proliferation which induced by TGF-β1 , but in the groups of rat serum medicated- high dose CBRP, the high level of cell secretion fibronectin, collagenⅠor collagenⅢwhich boosted by TGF-β1 had been decreased, especially the group of high dose CBRP had best effect (P<0. 01). Conclusion:In some extent CBRP could restrain renal interstitial fibroblast secrete or synthesize extracellular matrix such as FN, Col, ColⅢwhich enhanced by TGF-β1 , especially the high dose CBRP exert preferable effects.