In:
Annals of the New York Academy of Sciences, Wiley, Vol. 1043, No. 1 ( 2005-06), p. 681-684
Abstract:
A bstract : Advanced glycation end products (AGEs) have been associated with progressive vascular and renal damage in a variety of pathological conditions such as renal failure and diabetes mellitus. The formation of AGEs is generally attributed to increased oxidative and carbonyl stress or hyperglycemia. Activation of the cellular receptor of AGE (RAGE) leads to subsequent cellular activation and proinflammatory responses. Angiotensin (Ang) produces cellular oxidative stress and similarly promotes end organ damage via its type 1 receptor. We investigated the interrelation between these two systems in a new transgenic rat (TGR) model with Ang II‐dependent hypertension and renal damage and in nontransgenic controls. TGR showed increased systolic blood pressure (∼210 mmHg), proteinuria, and increased renal collagen I mRNA expression compared with normotensive nontransgenic controls. Immunohistochemical staining of kidney sections showed colocalization for N ε ‐carboxy(methyl)lysine, RAGE, and NF‐κB in TGR glomeruli. These features were absent in nontransgenic controls. Our observations suggest a possible link between Ang II‐dependent end‐organ damage and the AGE/RAGE axis in vivo . TGRs provide an excellent model to study the interrelation between the renin‐angiotensin system and the AGE/RAGE axis in promoting cardiovascular end‐organ damage, which would otherwise not be possible in humans.
Type of Medium:
Online Resource
ISSN:
0077-8923
,
1749-6632
DOI:
10.1196/annals.1333.078
Language:
English
Publisher:
Wiley
Publication Date:
2005
detail.hit.zdb_id:
2834079-6
detail.hit.zdb_id:
211003-9
detail.hit.zdb_id:
2071584-5
SSG:
11
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