Rl. Ryall et al., THE URINARY F1 ACTIVATION PEPTIDE OF HUMAN PROTHROMBIN IS A POTENT INHIBITOR OF CALCIUM-OXALATE CRYSTALLIZATION IN UNDILUTED HUMAN URINE IN-VITRO, Clinical science, 89(5), 1995, pp. 533-541
1. The urinary F1 activation peptide of prothrombin is the predominant
protein incorporated into calcium oxalate crystals precipitated from
human urine. The aim of this study was to examine the effect of pure u
rinary prothrombin F1 on calcium oxalate crystallization in human urin
e. 2. Urinary prothrombin F1 was purified from demineralized calcium o
xalate crystals precipitated from human urine, and its effects on calc
ium oxalate crystallization induced by addition of an oxalate load wer
e tested in undiluted, ultrafiltered urine from healthy men, at final
concentrations of 0 to 10 mg/l. 3. Urinary prothrombin F1 did not affe
ct the amount of oxalate required to induce crystallization, but the v
olume of material deposited increased in proportion to increasing conc
entrations of urinary prothrombin F1. However, the mean particle size
decreased in reverse order: this was confirmed by scanning electron mi
croscopy, which showed it to be the result of a reduction in crystal a
ggregation rather than in the size of individual crystals. Analysis of
C-14-oxalate data revealed a dose-dependent decrease in calcium oxala
te deposition with an increase in urinary prothrombin F1 concentration
, indicating that the increase in particle volume recorded by the Coul
ter Counter resulted from inclusion of urinary prothrombin F1 into the
crystalline architecture, rather than increased deposition of calcium
oxalate. 4. It was concluded that urinary prothrombin F1 may be an im
portant macromolecular determinant of stone formation.