当代医学
噹代醫學
당대의학
CHINA CONTEMPORARY MEDICINE
2014年
21期
9-10
,共2页
胰岛素样生长因子结合蛋白-2%肝星状细胞%贝那普利%实时荧光定量PCR
胰島素樣生長因子結閤蛋白-2%肝星狀細胞%貝那普利%實時熒光定量PCR
이도소양생장인자결합단백-2%간성상세포%패나보리%실시형광정량PCR
Insulin-like growth factor binding protein-2%Hepatic stellate cell%Benazepril%Realtime fluores-cence quantitative PCR
目的:探讨血管紧张素I (Angiotensin I ,AngI )及血管紧张素转化酶抑制剂贝那普利对体外培养的肝星状细胞胰岛素生长因子结合蛋白-2(insulin-like growth factor binding protein-2,IGFBP-2)mRNA表达的影响。方法采用肝星状细胞珠HSC-T 6作为研究模型,将培养的肝星状细胞分为对照组、AngI 组、贝那普利组和贝那普利+AngI 组采用实时荧光定量PCR(Realtime fluores-cence quantitative PCR,RTFQ PCR)的方法检测肝星状细胞中IGFBP-2 mRNA的表达水平。结果(1)在体外培养的肝星状细胞中AngI 组高于对照组,差异有统计学意义(P<0.05);(2)AngI+贝那普利组IGFBP-2 mRNA低于AngI组(P<0.05)。结论 AngI 能促进肝星状细胞IGFBP-2 mRNA表达,贝那普利的抗肝纤维化作用,可能与IGFBP-2 mRNA表达降低有关。
目的:探討血管緊張素I (Angiotensin I ,AngI )及血管緊張素轉化酶抑製劑貝那普利對體外培養的肝星狀細胞胰島素生長因子結閤蛋白-2(insulin-like growth factor binding protein-2,IGFBP-2)mRNA錶達的影響。方法採用肝星狀細胞珠HSC-T 6作為研究模型,將培養的肝星狀細胞分為對照組、AngI 組、貝那普利組和貝那普利+AngI 組採用實時熒光定量PCR(Realtime fluores-cence quantitative PCR,RTFQ PCR)的方法檢測肝星狀細胞中IGFBP-2 mRNA的錶達水平。結果(1)在體外培養的肝星狀細胞中AngI 組高于對照組,差異有統計學意義(P<0.05);(2)AngI+貝那普利組IGFBP-2 mRNA低于AngI組(P<0.05)。結論 AngI 能促進肝星狀細胞IGFBP-2 mRNA錶達,貝那普利的抗肝纖維化作用,可能與IGFBP-2 mRNA錶達降低有關。
목적:탐토혈관긴장소I (Angiotensin I ,AngI )급혈관긴장소전화매억제제패나보리대체외배양적간성상세포이도소생장인자결합단백-2(insulin-like growth factor binding protein-2,IGFBP-2)mRNA표체적영향。방법채용간성상세포주HSC-T 6작위연구모형,장배양적간성상세포분위대조조、AngI 조、패나보리조화패나보리+AngI 조채용실시형광정량PCR(Realtime fluores-cence quantitative PCR,RTFQ PCR)적방법검측간성상세포중IGFBP-2 mRNA적표체수평。결과(1)재체외배양적간성상세포중AngI 조고우대조조,차이유통계학의의(P<0.05);(2)AngI+패나보리조IGFBP-2 mRNA저우AngI조(P<0.05)。결론 AngI 능촉진간성상세포IGFBP-2 mRNA표체,패나보리적항간섬유화작용,가능여IGFBP-2 mRNA표체강저유관。
Objective To explore the effects of angiotensin II and angiotensin converting enzyme in-hibitor benazepril on insulin-like growth factor binding protein-2 mRNA (IGFBP-2 mRNA) expression of in vitro cultured hepatic stellate cell (HSC-T 6 ) cells. Methods HSC-T 6 rat hepatic stellate cells line was chosen as the study model. Cultured HSCs were randomized into the control group, AngII group, benazepril group and AngII+benazepril group. The expression of IGFBP-2 mRNA in different group was deteminned by the Realtime fluores-cence quantitative PCR RTFQ PCR meththod. Results Hepatic stellate cells in vitro culture of AngII group is higher than the control group (P<0.05). AngII+benazepril group were reduced than higher than the control group (P<0.05). Conclusion AngII can promote the hepatic stellate cells IGFBP-2 mRNA expression Benazepril decreases the expression IGFBP-2 mRNA in hepaic fibrosis which might inhibit the liver fibrosis.