Urinary-peptide excretion by patients with and volunteers without diabetes

被引:36
作者
Strong, KJ [1 ]
Osicka, TM [1 ]
Comper, WD [1 ]
机构
[1] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
来源
JOURNAL OF LABORATORY AND CLINICAL MEDICINE | 2005年 / 145卷 / 05期
关键词
D O I
10.1016/j.lab.2004.11.021
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Large quantities of peptides (1-4 g) are excreted in human urine each day. In this study we sought to analyze how peptide excretion varies with increasing albuminuria associated with diabetes, as well as to characterize the size distribution of albumin-derived peptides in urine from volunteers without diabetes and from patients with macroalbuminuria and diabetes. We detected albumin-derived peptides by injecting tritiated albumin intravenously into human volunteers and patients with diabetes. Urine was collected after 24 hours and fractionated on a size-exclusion column. This fractionation revealed peptides with molecular weights ranging from 300 to 500 Da in volunteers without diabetes. The albumin-derived peptides were of higher molecular weight in the urine of a patient with macroalbuminuria and diabetes. The molecular-weight distribution of the peptides derived from tritiated albumin peptides was paralleled by the distribution of all protein peptides (including albumin) as determined with the use of the Biuret protein assay or absorbance at 214 nm. We determined peptide-excretion rates by filtering urine from patients with diabetes through a 10,000 Da molecular-weight-cutoff membrane and then measuring the filtrate with the use of the Biuret assay. This analysis revealed that the peptide-excretion rate increased with increasing total protein excretion, regardless of whether the patient demonstrated normoalbuminuria or microalbuminuria. Among patients with macroalbuminuria, the peptide-excretion rate leveled off and even decreased in the face of an increasing albumin concentration or protein-excretion rate. This study confirms that albumin-derived and protein-derived peptides exist at high concentrations in urine. Although peptide-excretion rates are maintained at similar levels up to macroalbuminuric states, the relative proportion of peptide excretion is significantly reduced compared with total protein.
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收藏
页码:239 / 246
页数:8
相关论文
共 37 条
[1]  
ALTMAN DL, 1961, BLOOD BODY FLUIDS 1, P363
[2]   THE ROLE OF ASPARTIC AND CYSTEINE PROTEINASES IN ALBUMIN DEGRADATION BY RAT-KIDNEY CORTICAL LYSOSOMES [J].
BARICOS, WH ;
ZHOU, YW ;
FUERST, RS ;
BARRETT, AJ ;
SHAH, SV .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 256 (02) :687-691
[3]   Peptide mapping of proteins in human body fluids using electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry [J].
Bergquist, J ;
Palmblad, M ;
Wetterhall, M ;
Håkansson, P ;
Markides, KE .
MASS SPECTROMETRY REVIEWS, 2002, 21 (01) :2-15
[4]  
BUKTENICA S, 1987, J BIOL CHEM, V262, P9469
[5]   Alterations in renal degradation of albumin in early experimental diabetes in the rat: a new factor in the mechanism of albuminuria [J].
Burne, MJ ;
Panagiotopoulos, S ;
Jerums, G ;
Comper, WD .
CLINICAL SCIENCE, 1998, 95 (01) :67-72
[6]   Fractional clearance of high molecular weight proteins in conscious rats using a continuous infusion method [J].
Burne, MJ ;
Osicka, TM ;
Comper, WD .
KIDNEY INTERNATIONAL, 1999, 55 (01) :261-270
[7]   Albumin fragments in normal rat urine are derived from rapidly degraded filtered albumin [J].
Clavant, SP ;
Greive, KA ;
Nikolovski, J ;
Reeve, S ;
Smith, AI ;
Comper, WD .
NEPHROLOGY, 2003, 8 (02) :72-79
[8]   Exogenous albumin peptides influence the processing of albumin during renal passage [J].
Eppel, GA ;
Pratt, LM ;
Greive, KA ;
Comper, WD .
NEPHRON, 2002, 92 (01) :156-164
[9]   Variability of standard clinical protein assays in the analysis of a model urine solution of fragmented albumin [J].
Eppel, GA ;
Nagy, S ;
Jenkins, MA ;
Tudball, RN ;
Daskalakis, M ;
Balazs, NDH ;
Comper, WD .
CLINICAL BIOCHEMISTRY, 2000, 33 (06) :487-494
[10]   Albumin overload induces apoptosis in LLC-PK1 cells [J].
Erkan, E ;
De Leon, M ;
Devarajan, P .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2001, 280 (06) :F1107-F1114