当代医学
噹代醫學
당대의학
CHINA CONTEMPORARY MEDICINE
2013年
35期
5-7
,共3页
徐丽君%汤杰印%张祥贵%马华林
徐麗君%湯傑印%張祥貴%馬華林
서려군%탕걸인%장상귀%마화림
商陆皂苷甲%系膜细胞%细胞增殖%Caspase-3
商陸皂苷甲%繫膜細胞%細胞增殖%Caspase-3
상륙조감갑%계막세포%세포증식%Caspase-3
Esculentoside A%Glomerular mesangial cell%Cell proliferation%Caspase-3
目的:观察商陆皂苷甲(EsA)对白细胞介素1β(IL-1β)诱导的大鼠肾小球系膜细胞(rGMC)增殖及Caspase-3表达的影响,探讨EsA治疗狼疮性肾炎等系膜细胞增殖性肾小球肾炎的可能机制。方法 MTT法检测不同浓度的EsA对rGMC增殖的影响;蛋白质印迹法检测Caspase-3的表达,并成像分析。结果观察剂量中EsA对rGMC没有明显的细胞毒作用,EsA作用rGMC 48 h后抑制细胞增殖的有效浓度为2.5~5.0 mg/L(P<0.05或P<0.01);IL-1β促进了rGMC的Caspase-3的表达(P<0.01),与IL-1β组比较,EsA+IL-1β组对rGMC的Caspase-3的表达差异无统计学意义(P>0.05)。结论在体外EsA(2.5~5 mg/L)可显著抑制rGMC的增殖,GMC可能是EsA的作用靶细胞;但其促凋亡作用不明显。
目的:觀察商陸皂苷甲(EsA)對白細胞介素1β(IL-1β)誘導的大鼠腎小毬繫膜細胞(rGMC)增殖及Caspase-3錶達的影響,探討EsA治療狼瘡性腎炎等繫膜細胞增殖性腎小毬腎炎的可能機製。方法 MTT法檢測不同濃度的EsA對rGMC增殖的影響;蛋白質印跡法檢測Caspase-3的錶達,併成像分析。結果觀察劑量中EsA對rGMC沒有明顯的細胞毒作用,EsA作用rGMC 48 h後抑製細胞增殖的有效濃度為2.5~5.0 mg/L(P<0.05或P<0.01);IL-1β促進瞭rGMC的Caspase-3的錶達(P<0.01),與IL-1β組比較,EsA+IL-1β組對rGMC的Caspase-3的錶達差異無統計學意義(P>0.05)。結論在體外EsA(2.5~5 mg/L)可顯著抑製rGMC的增殖,GMC可能是EsA的作用靶細胞;但其促凋亡作用不明顯。
목적:관찰상륙조감갑(EsA)대백세포개소1β(IL-1β)유도적대서신소구계막세포(rGMC)증식급Caspase-3표체적영향,탐토EsA치료랑창성신염등계막세포증식성신소구신염적가능궤제。방법 MTT법검측불동농도적EsA대rGMC증식적영향;단백질인적법검측Caspase-3적표체,병성상분석。결과관찰제량중EsA대rGMC몰유명현적세포독작용,EsA작용rGMC 48 h후억제세포증식적유효농도위2.5~5.0 mg/L(P<0.05혹P<0.01);IL-1β촉진료rGMC적Caspase-3적표체(P<0.01),여IL-1β조비교,EsA+IL-1β조대rGMC적Caspase-3적표체차이무통계학의의(P>0.05)。결론재체외EsA(2.5~5 mg/L)가현저억제rGMC적증식,GMC가능시EsA적작용파세포;단기촉조망작용불명현。
Objective To observe the effects of Esculemoside A(EsA)on the proliferation and expression of Caspase-3 of rats glomerular mesangial cell(GMC)and to explore the mechanism by which EsA on effects Lupus nephritis(LN)and other GMC proliferation diseases.Methods rGMC was cultured in vitro, The cell growth were detected by MTT assay;The expression of Caspase-3 were measured by Western-Blot. Results The observed dose EsA has not apparent cytotoxicity effect on rGMC. After 48 h,inhibition proliferation concentration of EsA on rGMC was 2.5-5.0 mg/L;IL-1βpromoted the expression of Caspase-3 of rGMC(P<0.01).But there was no signiifcantly difference between IL-1βgroup and IL-1β+EsA group.Conclusion EsA(2.5-5 mg/L) can signiifcantly inhibit the proliferation of rGMC in vitro.The GMC is one of the mainly target cell. But the effect of promote apoptosis is not obvious.