Phasic production of urinary pyridinium crosslinks in mice: The effect of ovariectomy

Citation
R. Blanque et al., Phasic production of urinary pyridinium crosslinks in mice: The effect of ovariectomy, CALCIF TIS, 68(2), 2001, pp. 102-108
Citations number
25
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
CALCIFIED TISSUE INTERNATIONAL
ISSN journal
0171967X → ACNP
Volume
68
Issue
2
Year of publication
2001
Pages
102 - 108
Database
ISI
SICI code
0171-967X(200102)68:2<102:PPOUPC>2.0.ZU;2-I
Abstract
Considerable sample to sample variability in deoxypyridinoline crosslink/cr eatinine (Dpd/CREAT) ratio values was confirmed when twice-weekly sampling for 77 days was performed in C57 mice. Analysis of samples from individual mice indicated that, in the majority of mice in a given group (54-67%), pha sic changes occurred with peri odic peaks as much as 4-5 times basal values . Alignment of peaks in the individual time courses of mice revealed a clea r cyclic crosslink production (periodicity 12-14 days) for the population. although not all mice gave a peak in every case. Ovariectomy (OVX) (compare d to sham-operated mice) increased mean values of crosslink production by e ither C57 or C57 x 129 Fl mice from about 10 days after operation with high est values between 21 and 35 days, and then a decrease in the difference be tween sham and OVX, particularly in C57 mice. Analysis of both time courses for individual mice and distribution curves of the data from groups of mic e indicated that OVX consistently increased basal crosslink values (6-9 rat io units) with phasic peak values superimposed. The peak alignment analysis reinforced this observation. The influence of the background variability w as avoided by pooling data over one cycle time and the use of nonparametic statistics, and the effect of OVX was analyzed in several strains of mice. Crosslink levels and phasic production declined with age but were also infl uenced by manipulation of the mice, suggesting that experimental conditions should be rigorously controlled when this urinary crosslink measure is use d as a parameter in mouse models of OVX-induced osteoporosis.