Simvastatin suppresses expression of angiogenic factors in the retinas of rats with streptozotocin-induced diabetes

Simvastatin suppresses expression of angiogenic factors in the retinas of rats with streptozotocin-induced diabetes

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Sul Gee Lee & Jung Lim Kim & Han Kee Lee & Gyu Won Ryu & Dae Young Hur & Il Han Yun & Jae Wook Yang & Hyun Woong Kim
  • چاپ و سال / کشور: 2010

Description

Background Angiogenic factors such as vascular endothelial growth factor (VEGF), erythropoietin, and angiopoietin play important roles in the pathophysiology of diabetic retinopathy. Increased amounts of reactive oxygen species (ROS) are also known to associated with diabetic retinopathy and VEGF expression. This study evaluated the effect of a simvastatin on ROS generation and the changes in various angiogenic factors in the retinas of diabetic rats. Methods The rats were divided into normal, diabetes mellitus (DM), and simvastatin-treated groups (each group, n=10). Diabetes was induced by intraperitoneal injection of streptozotocin into 20 Sprague–Dawley rats. After diabetic induction, simvastatin (5mg/kg) was administered orally to ten rats. The expression levels of VEGF, erythropoietin, angiopoietin 1 and 2, and NADPH oxidase were examined in rat retinas by RT-PCR and Western blot. Superoxide formation was examined by dihydroethidium (DHE) staining. Results DHE analysis revealed increased superoxide formation in the retinas of the diabetic group, which was decreased in the group treated with simvastatin. Western blot analysis showed that NADPH oxidase levels were decreased in the diabetic group and remained normal in the simvastatin-treated group. Simvastatin treatment blocked hyperglycemia-induced increases in VEGF, angiopoietin 2 and erythropoietin levels, as demonstrated by RT-PCR and Western blot analysis. Conclusions Simvastatin treatment led to suppression of superoxide formation and decreased expression of VEGF, angiopoietin 2 and erythropoietin in diabetic rat retinas.
Graefes Arch Clin Exp Ophthalmol (2011) 249:389–397 DOI 10.1007/s00417-010-1496-5 Received: 22 December 2009 / Revised: 9 July 2010 / Accepted: 16 August 2010 / Published online: 7 September 2010
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