Background: Uroguanylin, originally isolated from urine, is a new natriuretic peptide. Its plasma level is increased in association with renal impairment and fluid retention in patients with renal diseases. Methods: Uroguanylin concentrations were measured in patients on hemodialysis (HD, n = 76) and those on continuous ambulatory peritoneal dialysis (CAPD, n = 10) using a sensitive ra- dioimmunoassay for human uroguanylin. Results: Plasma concentrations of immunoreactive (ir)-uroguanylin in the patients on HD and CAPD (212.0 ± 17.4 and 245.3 ± 39.5 fmol/ml) were significantly higher than the value for the normal controls (5.0 ± 0.3 fmol/ml). Plasma ir-uroguanylin levels before the start of regular HD were correlated with predialysis excess weight based on their dry weights (r = 0.33, p < 0.01) and with dialysis duration (r = 0.26, p < 0.05). The plasma levels in patients with HD, for whom high-flux membranes were used, were decreased at the end of regular HD as compared with the prior levels (p < 0.05), but not in those who underwent HD with conventional membranes. Conclusion: These findings suggest that the plasma ir-uroguanylin level is related to the patient’s volume status as well as renal impairment. Whether the accumulation of uroguanylin has a pathological effect has yet to be determined.

1.
Greenberg RN, Hill M, Crytzer J, Krause WJ, Eber SL, Hamra FK, Forte LR: Comparison of effects of uroguanylin, guanylin, and Escherichia coli heat-stable enterotoxin STa in mouse intestine and kidney. J Invest Med 1997;45:276–283.
2.
Fonteles MC, Greenberg RN, Monteiro HS, Currie MG, Forte LR: Natriuretic and kaliuretic activities of guanylin and uroguanylin in the isolated perfused rat kidney. Am J Physiol 1998;275:F191–F197.
3.
Kinoshita H, Fujimoto S, Nakazato M, Yokota N, Date Y, Yamaguchi H, Hisanaga S, Eto T: Urine and plasma levels of uroguanylin and its molecular forms in renal diseases. Kidney Int 1997;52:1028–1034.
4.
Forte LR, Fan X, Harma FK: Salt and water homeostasis: Uroguanylin is a circulating peptide hormone with natriuretic activity. Am J Kidney Dis 1996;28:296–304.
5.
Miyazato M, Nakazato M, Yamaguchi H, Date Y, Kojima M, Kangawa K, Matsuo H, Matsukura S: Cloning and characterization of a cDNA encoding a precursor for human uroguanylin. Biochem Biophys Res Commun 1996;219:644–648.
6.
Hill O, Cetin Y, Cieslak A, Mägert HJ, Forssmann WG: A new human guanylate cyclase-activating peptide (GCAP-, uroguanylin): Precursor cDNA and colonic expression. Biochim Biophys Acta 1995;1253:146–149.
7.
Nakazato M, Yamaguchi H, Kinoshita H, Kangawa K, Matsuo H, Chino N, Matsukura S: Identification of biologically active and inactive human uroguanylin in plasma and urine and their increases in renal insufficiency. Biochem Biophys Res Commun 1996;220:586–593.
8.
Kinoshita H, Fujimoto S, Fukae H, Yokota N, Hisanaga S, Nakazato M, Eto T: Plasma and urine levels of uroguanylin, a new natriuretic peptide, in nephrotic syndrome. Nephron 1999;81:160–164.
9.
Kinoshita H, Nakazato M, Yamaguchi H, Matsukura S, Fujimoto S, Eto T: Increased plasma guanylin levels in patients with impaired renal function. Clin Nephrol 1997;47:28–32.
10.
Plum J, Grabensee B: Atrial natriuretic peptide in dialysis patients under various conditions of volume homeostasis. J Intern Med 1991;229:209–216.
11.
Shiota J, Kubota M, Hamada C, Koide H: Plasma atrial natriuretic peptide during hemodialysis with or without fluid removal. Nephron 1990;55:283–286.
12.
Yamamoto Y, Higa T, Kitamura K, Tanaka K, Kangawa K, Matsuo H: Plasma concentration of human atrial natriuretic polypeptide in patients with impaired renal function. Clin Nephrol 1987;27:84–86.
13.
Ando R, Matyuda O, Miyake S, Yoshiyama N: Plasma levels of human atrial natriuretic factor in patients treated by hemodialysis and continuous ambulatory dialysis. Nephron 1988;50:225–228.
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