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Departments of Gastrointestinal Surgery and Clinical Biochemistry, Rigshospitalet, University of Copenhagen, DK-2100 Copenhagen, Denmark
The renal handling of carboxyamidated gastrins,
NH2-terminal progastrin fragments,
and glycine-extended gastrins was examined in healthy volunteers. The
respective urinary clearances after a meal amounted to 0.09 ± 0.02%, 0.17 ± 0.04% (P < 0.05), and 0.04 ± 0.01% (P < 0.01) of the glomerular filtration rate. During intravenous
infusion of carboxyamidated gastrin-17, progastrin fragment-(1
35),
and glycine-extended gastrin-17, the respective urinary clearances
amounted to 0.08 ± 0.02, 0.46 ± 0.08, and 0.02 ± 0.01%,
respectively, of the glomerular filtration rate. The metabolic
clearance rate of the three peptides was 24.4 ± 1.3, 6.0 ± 0.4, and 8.6 ± 0.7 ml · kg
1 · min
1.
A maximum rate for tubular transport or degradation of the peptides could not be determined, nor was a renal plasma threshold recorded. Plasma concentrations and urinary excretion rates correlated for gastrin-17 and progastrin fragment-(1
35)
(r = 0.94 and 0.97, P < 0.001), whereas the excretion of
glycine-extended gastrin diminished with increasing plasma
concentrations. We conclude that renal excretion of progastrin products
is negligible compared with renal metabolism and that renal handling of
the peptides depends on their molecular structure. Hence, the kidneys
exhibited a higher excretion of
NH2-terminal progastrin fragments
than of carboxyamidated and especially glycine-extended gastrins.
gastrointestinal peptides; metabolism; urinary excretion
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