Lin Shu-Dian, Zhou Qiao-Ling, Zhan Feng, Chen Dao-Jun, Li Wen-Ning
Department of Nephrology, Hainan Province Hospital, Haikou 570001, China.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2010 Aug;26(3):348-51.
To investigate the effect of fosinopril (Fos) on regulating klotho gene expression and elucidate the mechanism of Fos regulating the Angiotensin II (AngII) -induced down-expression of klotho gene.
Culture cells, NRK-52E, were incubated with media either AngII or Fos or both of all. Experimental groups incubated with Fos (10(-5) mol/L) were divided according to variant points of time for 0 (control), 3, 6, 12, 24 h. Different concentration of Fos was selected to incubated with culture cells for 0 (control), 10(-9) 10(-8), 10(-7), 10(-6), 10(-5) mol/L at the optimal time point (24 h). Five groups, which were A: control; B: AngII (10(-7) mol/L); C: Fos(10(-5) mol/L); D: AngII (10(-7) mol/L) + Fos(10(-5) mol/L) and E: Cells pretreated with Fos(10(-5) mol/L)12 h incubated with AngII (10(-7) mol/L) were divided to observe the effect of Fos on expression of klotho induced by AngII. RT-PCR and immunohistochemistry (IHC) were applied to evaluate the klotho mRNA and protein expression, respectively.
Fos up-regulated klotho mRNA in time-dependent manner, and independent of dose-dependent manner; AngII obviously decreased the levels of kloltho mRNA and protein expression in NRK-52E as compared to the control (P < 0.05), the down-regulating effect was reversed by incubating both with AngII and Fos (P < 0.05), and Fos could inhibit the down-regulated expression of klotho gene induced by Ang II in NRK-52E.
Fosinopril up-regulates klotho mRNA in time-dependent manner, and inhibits the down-regulated expression of klotho gene induced by Ang II.
探讨福辛普利(Fos)对klotho基因表达的调控作用,阐明Fos调控血管紧张素II(AngII)诱导的klotho基因下调表达的机制。
用AngII、Fos或二者共同处理培养的NRK-52E细胞。将用Fos(10(-5)mol/L)处理的实验组按不同时间点分为0(对照)、3、6、12、24小时组。在最佳时间点(24小时)选择不同浓度的Fos(0(对照)、10(-9)、10(-8)、10(-7)、10(-6)、10(-5)mol/L)与培养细胞孵育。分为五组,A:对照;B:AngII(10(-7)mol/L);C:Fos(10(-5)mol/L);D:AngII(10(-7)mol/L)+Fos(10(-5)mol/L);E:先用Fos(10(-5)mol/L)预处理12小时后再用AngII(10(-7)mol/L)孵育的细胞,观察Fos对AngII诱导的klotho表达的影响。分别应用RT-PCR和免疫组织化学(IHC)评估klotho mRNA和蛋白表达。
Fos以时间依赖性方式上调klotho mRNA,且与剂量无关;与对照组相比,AngII明显降低NRK-52E中kloltho mRNA和蛋白表达水平(P<0.05),AngII和Fos共同孵育可逆转这种下调作用(P<0.05),Fos可抑制Ang II诱导的NRK-52E中klotho基因的下调表达。
福辛普利以时间依赖性方式上调klotho mRNA,并抑制Ang II诱导的klotho基因下调表达。