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厄贝沙坦对糖尿病大鼠肾脏GluT-1及TGF-β1表达的影响及其临床意义

Effect of irbesartan on mRNA expression of GLUT-1 and TGFβ-1 in the kidney of diabetic rats and the clinical significance
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摘要 目的观察厄贝沙坦(IBST)对糖尿病大鼠肾脏皮质葡萄糖转运蛋白-1(GluT-1)及转化生长因子-β1(TGF-β1)表达的影响,并探讨其作用机制。方法 48只大鼠随机分为对照(Con)组、糖尿病(DM)组与IBST治疗组,建立糖尿病肾病(DN)模型,分别检测肾皮质GluT-1 mRNA及TGF-β1 mRNA表达水平。结果与Con组相比,DM组大鼠肾组织GluT-1 mRNA表达及TGF-β1 mRNA表达均显著上调(P<0.01)。厄贝沙坦干预后,IBST组肾组织GluT-1及TGF-β1 mRNA表达显著低于DM组(P<0.01)。结论厄贝沙坦对DN有保护作用,这可能与厄贝沙坦显著降低肾组织G1uT-1及TGF-β1 mRNA表达有关。 Objective To investigate the effect of irbesartan, on the mRNA expressions of GluT-1 and TGF-β1 in the kidney of diabetic rats, and investigate their clincal significance, Methods The 34 STZ-indnced diabetic Wistar rats were divided into simple diabetes(group B,n= 17) and irbesartan-treated diabetes (group C,n= 17) ,and 14 healthy rats were used as control (group A). The body weight,plasma glucose,serum creatinine,blood urea nitrogen,cholesterol,triglyceried,24-hour urinary protein excretion were measured in each rat. The renal tissues were examined histologically by HE staining and PAS staining. Renal mRNA expression of GluT-1 and TGF-β1 were detected by RT-PCIL Results The plasma glucose,serum creatinine,blood urea nitrogen,cholesterol,triglyceried, 24-hour urinary protin excretion, renal rnRNA expression of GluT-1 and TGF-β1 were increased significantly in group B versus group A. (P〈0.01). 24-hour urinary protein excretion, serum creatinine and blood urea nitrogen were decreased significantly in gruop C versus group B. Renal mRNA expression of GluT-1 and TGF-β1 decreased significantly (P〈0. 01). Conclusions Irbesartan can prevent the injury of renal function in STZ-induced diabetic rats. The mechanism might be related to the suppression of expression of GluT- 1 and TGF-β1 mRNA.
出处 《中国糖尿病杂志》 CAS CSCD 北大核心 2009年第6期477-478,480,共3页 Chinese Journal of Diabetes
关键词 糖尿病肾病 葡萄糖转运蛋白-1 转化生长因子-Β1 厄贝沙坦 Diabetic nephropathy Glucose transport protein-1 Transforming growth factor-β1 Irbesarta
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参考文献4

  • 1Soldatos G,Cooper ME.Diabetic nephropathy:important pathophysiologic mechanisms.Diabetes Res Clin Pract,2008,82:S75-S79.
  • 2Heilig CW,Brosius FC,Cunningham C.Role for GluT-1 in diabetic glomerulosclerosis.Expert Rev Mol Med,2006,8:1-18.
  • 3Wang A,Ziyadeh FN,Lee EY,et al.Interference with TGF-beta signaling by Smad3-knockout in mice limits diabetic glomerulosclerosis without affecting albuminuria.Am J Physiol Renal Physiol,2007,293:F1657-F1665.
  • 4Wang G,Lai FM,Lai KB,et al.Urinary mRNA expression of ACE and ACE2 in human type 2 diabetic nephropathy.Diabetologia,2008,51:1062-1067.

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