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Erschienen in: Diabetologia 8/2005

01.08.2005 | Article

Renal accumulation and clearance of advanced glycation end-products in type 2 diabetic nephropathy: effect of angiotensin-converting enzyme and vasopeptidase inhibition

verfasst von: C. Wihler, S. Schäfer, K. Schmid, E. K. Deemer, G. Münch, M. Bleich, A. E. Busch, T. Dingermann, V. Somoza, J. W. Baynes, J. Huber

Erschienen in: Diabetologia | Ausgabe 8/2005

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Abstract

Aims/hypothesis

Renal accumulation of AGEs may contribute to the progression of diabetic nephropathy. We evaluated the effect of ramipril (a pure ACE inhibitor) and AVE7688 (a dual inhibitor of ACE and neutral endopeptidase) on renal accumulation of the advanced glycation end-product (AGE) 3-deoxyglucosone-imidazolone, carboxymethyllysine (CML) and pentosidine, and on clearance of CML in type 2 diabetes.

Methods

Male Zucker diabetic fatty rats (ZDF, Gmi-fa/fa) rats were treated from age 10 to 37 weeks with ramipril (1 mg·kg−1·day−1), AVE7688 (45 mg·kg−1·day−1) or without drug. Ramipril and AVE7688 reduced albuminuria by 30 and 90%, respectively.

Results

ZDF rats showed increased renal accumulation of the AGE subtypes 3-deoxyglucosone-imidazolone, pentosidine and CML by about 40, 55 and 55%, respectively compared with heterozygous, non-diabetic control animals at the age of 37 weeks. AVE7688 but not ramipril attenuated the renal accumulation of 3-deoxyglucosone-imidazolone, pentosidine and CML and improved CML clearance in ZDF rats. During glycation reactions in vitro, AVE7688 also demonstrated potent chelating activity and inhibited metal-catalysed formation of pentosidine and CML.

Conclusions/interpretation

Improved AGE clearance and direct inhibition of AGE formation by chelation may contribute to reduced accumulation of renal AGEs and to the nephroprotective effects of vasopeptidase inhibition in type 2 diabetes.
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Metadaten
Titel
Renal accumulation and clearance of advanced glycation end-products in type 2 diabetic nephropathy: effect of angiotensin-converting enzyme and vasopeptidase inhibition
verfasst von
C. Wihler
S. Schäfer
K. Schmid
E. K. Deemer
G. Münch
M. Bleich
A. E. Busch
T. Dingermann
V. Somoza
J. W. Baynes
J. Huber
Publikationsdatum
01.08.2005
Erschienen in
Diabetologia / Ausgabe 8/2005
Print ISSN: 0012-186X
Elektronische ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-005-1837-9

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