Advanced oxidation protein products accelerate renal fibrosis in a remnant kidney model

• Published in: Journal of the American Society of Nephrology 2007-02, Vol.18 (2), p.528-538
• Main Authors: Li, Hong Yan, Hou, Fan Fan, Zhang, Xun, Chen, Ping Yan, Liu, Shang Xi, Feng, Jian Xun, Liu, Zhi Qiang, Shan, Yue Xin, Wang, Guo Bao, Zhou, Zhan Mei, Tian, Jian Wei, Xie, Di
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Blood Pressure; Disease Models, Animal; Disease Progression; Fibrosis; Kidney - pathology; Kidneys; Male; Medical sciences; Nephrology. Urinary tract diseases; Oxidation-Reduction; Proteins - metabolism; Rats; Rats, Sprague-Dawley; Urinary system involvement in other diseases. Miscellaneous
• ISSN: 1046-6673; 1533-3450
• DOI: 10.1681/asn.2006070781

Accumulation of plasma advanced oxidation protein products (AOPP) has been found in patients with chronic kidney disease. However, the biologic consequences of AOPP consumption on progression of renal disease still are unclear. For testing of the hypothesis that AOPP accelerate progression of chronic kidney disease, Sprague-Dawley rats were subjected to five-sixths nephrectomy (5/6 Nx) or to sham operation. Rats in each group were randomly assigned in three subgroups (n = 30 in each group) and treated with repeated intravenous injections of AOPP-modified rat serum albumin (RSA), unmodified RSA, or vehicle for indicated period. Compared with RSA- or vehicle-treated 5/6 Nx rats, AOPP RSA-treated 5/6 Nx rats displayed greater proteinuria, higher serum creatinine, and lower creatinine clearance. AOPP challenge resulted in more renal hypertrophy, higher macrophage influx, and greater renal fibrosis in the remnant kidney. Chronic administration of AOPP in sham-operated rats increased urinary protein excretion and renal macrophage infiltration, but histologic renal fibrosis was not observed during the study period. AOPP treatment enhanced AOPP level in renal tissue. This was associated with marked increase of thiobarbituric acid reactive substances, decrease of glutathione peroxidase activity, and upregulated expression of monocyte chemoattractant protein-1 and TGF-beta1 in renal cortex. These data indicate that AOPP might be a new and potentially important mediator of renal fibrosis in the remnant kidney. Chronic accumulation of AOPP promotes renal fibrosis probably via a redox-sensitive inflammatory pathway.