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Systemic and local effects of angiotensin II blockade in experimental diabetic nephropathyEndocrinology Department. Ramon y Cajal Hospital, Madrid, Spain, vieitezp{at}yahoo.com
Laboratory of Neuroinflammation, Experimental Neurology Department, Paraplegic National Hospital, Toledo, Spain, ogomezt{at}sescam.jccm.es
Life Science Division, NASA Ames Research Centre, Moffet Field, CA, USA
Endocrinology Department. Ramon y Cajal Hospital, Madrid, Spain
Laboratory of Neuroinflammation, Experimental Neurology Department, Paraplegic National Hospital, Toledo, Spain
Introduction. Our objective was to evaluate the effect of blocking the renin-angiotensin system (RAS) on the expression of transforming growth factor-beta 1 (TGF-β1), platelet derived growth factor-B (PDGF-B), tumour necrosis factor-alpha (TNF-
Materials and Method. 1) Uninephrectomised streptozotocin induced diabetic rats were treated during eight months with vehicle (CD) or irbesartan (ID). Uninephrectomised non-diabetic rats were used as control group (ND). Protein urinary excretion and morphological renal damage were analysed. Glomerular expression of TGF-β1, PDGF-B, VEGF and TNF-
Results. ND and ID presented lower renal injury and proteinuria than CD (p<0.05). Glomerular expression of TGF-β1, PDGF-B,TNF-
Conclusion. Systemic and local administration of irbesartan lowers glomerular expression of TGF-β1, PDGF-B, VEGF and TNF-
Key Words: angiotensin receptor blockers diabetic nephropathy glomeruli growth factors renin-angiotensin system
Journal of Renin-Angiotensin-Aldosterone System, Vol. 9, No. 2,
96-102 (2008) |
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) and vascular endothelial growth factor (VEGF) in diabetic kidney glomeruli.