The effects of valsartan on the accumulation of circulating and renal advanced glycation end products in experimental diabetes

Josephine M. Forbes, Merlin C. Thomas, Suzanne R. Thorpe, Nathan L. Alderson, Mark E. Cooper

Research output: Contribution to journalArticleResearchpeer-review

32 Citations (Scopus)

Abstract

Background. Blockade of the RAS with the ACE inhibitor ramipril prevents the accumulation of advanced glycation end products (AGEs) in experimental diabetes. Although AT1 receptor antagonists may inhibit AGE formation in vitro, their effect in normotensive animals with type 1 diabetes has not been established. Methods. Streptozotocin-induced diabetic and control animals were randomized (N = 10/group) to receive the AT1 antagonist valsartan at a dose of 30 mg/kg/day by oral gavage for 24 weeks, or no intervention. Renal and plasma AGE accumulation was correlated with renal functional parameters. Results. Valsartan reduced the albumin excretion rate consistent with its renoprotective effects. Renal and skin collagen accumulation of the non-fluorescent AGE carboxymethyllysine (CML) were increased in animals with diabetes, but normalized following treatment with valsartan. Renal fluorescence and skin collagen pentosidine levels were also increased by diabetes. However, valsartan only provided a modest attenuation of these parameters. In addition, diabetes was associated with increased plasma fluorescence, which was unaffected by AT1 antagonism. Conclusion. Renoprotective doses of valsartan are associated with a significant reduction in the accumulation of tissue and plasma CML. These effects were not the same for all AGEs, suggesting combination approaches will be required to optimize renoprotection in diabetes.

Original languageEnglish
Pages (from-to)105-107
Number of pages3
JournalKidney International, Supplement
Volume66
Issue number92
DOIs
Publication statusPublished - 1 Nov 2004
Externally publishedYes

Keywords

  • Albuminuria
  • CML
  • Diabetic nephropathy

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