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Complications

Reduction of the Accumulation of Advanced Glycation End Products by ACE Inhibition in Experimental Diabetic Nephropathy

  1. Josephine M. Forbes1,
  2. Mark E. Cooper1,
  3. Vicki Thallas1,
  4. Wendy C. Burns1,
  5. Merlin C. Thomas1,
  6. Gail C. Brammar1,
  7. Fiona Lee1,
  8. Sharon L. Grant1,
  9. Louise M. Burrell1,
  10. George Jerums2 and
  11. Tanya M. Osicka2
  1. 1Department of Medicine, University of Melbourne, Austin and Repatriation Medical Centre, West Heidelberg, Australia
  2. 2Department of Endocrinology, Austin and Repatriation Medical Centre, Heidelberg, Australia
Diabetes 2002 Nov; 51(11): 3274-3282.
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This article has corrections. Please see:

  • Errata - December 01, 2002
  • Errata - April 01, 2010

Abstract

The effect of ACE inhibition on the formation of advanced glycation end products (AGEs) and oxidative stress was explored. Streptozocin-induced diabetic animals were randomized to no treatment, the ACE inhibitor ramipril (3 mg/l), or the AGE formation inhibitor aminoguanidine (1 g/l) and followed for 12 weeks. Control groups were followed concurrently. Renal AGE accumulation, as determined by immunohistochemistry and both serum and renal fluorescence, were increased in diabetic animals. This was attenuated by both ramipril and aminoguanidine to a similar degree. Nitrotyrosine, a marker of protein oxidation, also followed a similar pattern. The receptor for AGEs, gene expression of the membrane-bound NADPH oxidase subunit gp91phox, and nuclear transcription factor-κB were all increased by diabetes but remained unaffected by either treatment regimen. Two other AGE receptors, AGE R2 and AGE R3, remained unchanged for the duration of the study. The present study has identified a relationship between the renin-angiotensin system and the accumulation of AGEs in experimental diabetic nephropathy that may be linked through oxidative stress

Footnotes

  • Address correspondence and reprint requests to Dr. Josephine Forbes, Diabetes, Metabolism and Lipoproteins, Level 3, Baker Medical Research Institute, P.O. Box 6492, Prahran, VIC 3081, Australia. E-mail: josephine.forbes{at}baker.edu.au.

    Received for publication 10 April 2002 and accepted in revised form 22 July 2002.

    ACEI, ACE inhibitor; AER, albumin excretion rate; AGE, advanced glycation end product; CML, carboxymethyllysine; EMSA, electrophoretic mobility shift assay; GFR, glomerular filtration rate; NF-κB, nuclear factor-κB; NO, nitric oxide; PKC, protein kinase C; PMSF, phenylmethylsulfonyl fluoride; RAS, renin-angiotensin system; RAGE, receptor for AGEs; ROS, reactive oxygen species; rRNA, ribosomal RNA.

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Reduction of the Accumulation of Advanced Glycation End Products by ACE Inhibition in Experimental Diabetic Nephropathy
Josephine M. Forbes, Mark E. Cooper, Vicki Thallas, Wendy C. Burns, Merlin C. Thomas, Gail C. Brammar, Fiona Lee, Sharon L. Grant, Louise M. Burrell, George Jerums, Tanya M. Osicka
Diabetes Nov 2002, 51 (11) 3274-3282;

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Reduction of the Accumulation of Advanced Glycation End Products by ACE Inhibition in Experimental Diabetic Nephropathy
Josephine M. Forbes, Mark E. Cooper, Vicki Thallas, Wendy C. Burns, Merlin C. Thomas, Gail C. Brammar, Fiona Lee, Sharon L. Grant, Louise M. Burrell, George Jerums, Tanya M. Osicka
Diabetes Nov 2002, 51 (11) 3274-3282;
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