The involvement of growth hormone (GH), insulin-like growth factors (IGFs) and vascular endothelial growth factor (VEGF) in diabetic kidney disease

被引:41
作者
Flyvbjerg, A
Khatir, DS
Jensen, LJN
Dagnæs-Hansen, F
Gronbaek, H
Rasch, R
机构
[1] Aarhus Univ Hosp, Med Res Labs, Med Dept M, Inst Clin, DK-8000 Aarhus C, Denmark
[2] Univ Aarhus, Dept Microbiol, Aarhus, Denmark
[3] Aarhus Univ Hosp, Med Dept 5, Aarhus, Denmark
[4] Aarhus Univ, Inst Anat, Aarhus, Denmark
[5] Aarhus Univ Hosp, Dept Electron Microscopy, Aarhus, Denmark
关键词
growth factor; cytokine; mouse; rat; diabetic nephropathy;
D O I
10.2174/1381612043383106
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
At present, diabetic kidney disease affects about 15-25 % of patients with type I diabetes (TID) and 30-40 % of patients with type 2 diabetes (T2D). Several decades of extensive research have elucidated various pathways to be implicated in the development of diabetic kidney disease. These include metabolic factors beyond blood glucose (e.g. advanced glycation endproducts (AGEs)), haemodynamic factors (e.g. the renin angiotensin system (RAS)), intracellular signaling molecule proteins (e.g. protein kinase C (PKC)) and growth factors/cytokines (e.g. growth hormone (GH), insulin-like growth factors (IGFs), transforming growth factor beta (TGF-beta) and vascular endothelial growth factor (VEGF)). This review focusses on the role of three of these growth factors, i.e. GH, IGFs and VEGF. A brief discussion of each system is followed by description of its expression in the normal kidney. Then, for each system, in vitro, experimental and clinical evidence addressing the role of the system in diabetic kidney disease is presented. The interplay of each system to other potential pathways will also be adressed. Finally, well-known and potential therapeutic strategies targeting the GH/IGF and VEGF systems in a specific or indirect way will discussed.
引用
收藏
页码:3385 / 3394
页数:10
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