Mammary-specific deletion of parathyroid hormone–related protein preserves bone mass during lactation
J. Clin. Invest. Joshua N. VanHouten, et al. 112:1429 doi:10.1172/JCI19504 [
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Figure 3Calcium metabolism in
BLG-Cre/PTHrPlox/– mice. Circulating PTHrP(1–34) levels (
a) were significantly lower (
P < 0.05) during lactation in
BLG-Cre/PTHrPlox/– mice (0.73 ± 0.13 pM,
n = 7) than in
PTHrPlox/– controls (1.18 ± 0.19 pM,
n = 3). Circulating calcium (
b) and PTH (
c) concentrations were not significantly different between
PTHrPlox/– and
BLG-Cre/PTHrPlox/– mice during lactation. Probably as a result of the reduced circulating PTHrP, urinary cAMP levels (
d) and circulating 1,25-dihydroxy vitamin D concentrations (
e) were also significantly reduced. Milk calcium (
f) was not significantly different in
BLG-Cre/PTHrPlox/– mice and controls. Bars represent the mean values of 3–12 samples. PTH concentrations were 3.8 ± 1.5 pM in
PTHrPlox/– controls and 3.7 ± 0.9 pM in
BLG-Cre/PTHrPlox/– mice. Although statistically insignificant, both plasma calcium and milk calcium are slightly lower in
BLG-Cre/PTHrPlox/– mice (8.8 ± 0.2 mg/dl and 406.7 ± 39.4 mg/dl,
n = 14) than in controls (9.0 ± 0.3 mg/dl and 471 ± 78.5 mg/dl,
n = 9). Urinary cAMP was 33.9 ± 0.6 μg/mmol creatinine in
PTHrPlox/– controls (
n = 7) and 19.3 ± 0.8 μg/mmol creatinine in
BLG-Cre/PTHrPlox/– mice (
n = 11), while 1,25-dihydroxy vitamin D levels were 55.9 ± 5.9 pg/ml in
PTHrPlox/– mice (
n = 3) and 43.5 ± 2.2 pg/ml in
BLG-Cre/PTHrPlox/– mice (
n = 6).