Wang Li-Hui, Wu Guang-Li, Zhang Li-Xia, Huang Xu-Dong, Li Sai
Department of Nephrology, Bethune International Peace Hospital of PLA, Shijiazhuang 050082, China.
Yao Xue Xue Bao. 2009 Feb;44(2):121-5.
This study is to investigate the effects of fluvastatin on the activation of p38 mitogen-activated protein kinase (p38 MAPK) and cAMP response element-binding protein (CREB1) in glomerular mesangial cells under high concentration of glucose. High concentration glucose and fluvastatin were used to stimulate the cultured rat glomerular mesangial cells (GMCs) in vitro. The protein expressions of p38 MAPK, CREB1, p-p38 MAPK and p-CREB1 were observed with Western blotting. TGF-beta1 and fibronectin (FN) mRNA were measured with reverse transcription and polymerase chain reaction (RT-PCR). The protein synthesis of laminine (LN) and type IV collagen in the supernatants of the GMCs were detected with radioimmunoassay. Compared with low glucose control group, the expressions of p-p38 MAPK, p-CREB1 were increased obviously in high glucose group, TGF-beta1 mRNA and FN mRNA, LN and type IV collagen in the supernatants were increased significantly in GMCs under high concentration glucose medium. The expression levels of p-p38 MAPK, p-CREB1, TGF-beta1 mRNA, and FN mRNA, LN and type IV collagen in the supernatants were significantly lower in the fluvastatin group than those in the high concentration glucose group. It is concluded that fluvastatin can inhibit over production of TGF-beta1 and ECM proteins in GMCs under high concentration of glucose, partly by regulating the phosphorylation of p38 MAPK and CREB1.
本研究旨在探讨氟伐他汀对高糖环境下肾小球系膜细胞中p38丝裂原活化蛋白激酶(p38 MAPK)和环磷酸腺苷反应元件结合蛋白(CREB1)激活的影响。采用高糖和氟伐他汀体外刺激培养的大鼠肾小球系膜细胞(GMCs)。通过蛋白质免疫印迹法观察p38 MAPK、CREB1、磷酸化p38 MAPK(p-p38 MAPK)和磷酸化CREB1(p-CREB1)的蛋白表达。采用逆转录聚合酶链反应(RT-PCR)检测转化生长因子-β1(TGF-β1)和纤连蛋白(FN)mRNA。采用放射免疫分析法检测GMCs培养上清液中层粘连蛋白(LN)和IV型胶原的蛋白合成。与低糖对照组相比,高糖组p-p38 MAPK、p-CREB1表达明显增加,高糖培养基中GMCs的TGF-β1 mRNA、FN mRNA、培养上清液中的LN和IV型胶原显著增加。氟伐他汀组p-p38 MAPK、p-CREB1、TGF-β1 mRNA、FN mRNA、培养上清液中的LN和IV型胶原表达水平明显低于高糖组。结论:氟伐他汀可部分通过调节p38 MAPK和CREB1的磷酸化,抑制高糖环境下GMCs中TGF-β1和细胞外基质蛋白的过度产生。