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Citations to this article

Normal regulation of calcitriol production in Gy mice. Evidence for biochemical heterogeneity in the X-linked hypophosphatemic diseases.
G A Davidai, … , T Nesbitt, M K Drezner
G A Davidai, … , T Nesbitt, M K Drezner
Published February 1, 1990
Citation Information: J Clin Invest. 1990;85(2):334-339. https://doi.org/10.1172/JCI114442.
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Research Article

Normal regulation of calcitriol production in Gy mice. Evidence for biochemical heterogeneity in the X-linked hypophosphatemic diseases.

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Abstract

Phenotypic heterogeneity in X-linked hypophosphatemic rickets (XLH) is ascribed to variable penetrance of the genetic abnormality. However, studies of hypophosphatemic (Hyp) and gyrorotary (Gy) mice indicate that mutations at different loci along the X chromosome may underlie the genetically transmitted hypophosphatemic disorders. Thus, genetic heterogeneity may be a determinant of the phenotypic variability in XLH. To determine if such variance includes biochemical diversity, we examined whether Gy mice, similar to Hyp mice, exhibit abnormal regulation of renal 25-hydroxyvitamin D (25[OH]D)-1 alpha-hydroxylase. Serum phosphorus in Gy (4.7 +/- 0.3 mg/dl) and phosphate (P)-depleted mice (4.9 +/- 0.4) was significantly less than normal (8.4 +/- 0.5). Consistent with P depletion, the Gy mice exhibited enhanced renal 25(OH)D-1 alpha-hydroxylase activity (9.3 +/- 0.6 fmol/mg kidney per min), similar to that of P-depleted normals (9.1 +/- 1.5), but significantly greater than that of controls (3.1 +/- 0.3). Such normal enzyme responsiveness was confirmed upon PTH stimulation (1 IU/h s.c.), which revealed that Gy mice increased renal 1-hydroxylase (59 +/- 7.7) similarly to normals (65 +/- 7.7) and P-depleted animals (58.4 +/- 7.8). Calcitonin administration also enhanced enzyme function comparably in the animal models. Evidence confirming normally responsive calcitriol production in untreated Gy mice included increased serum 1,25-dihydroxyvitamin D levels, gastrointestinal calcium absorption, and urinary calcium. The normally regulated vitamin D metabolism in Gy mice indicates that biochemically diverse disease may result from mutations in the gene family regulating renal P transport and underlying X-linked hypophosphatemia. We suspect such heterogeneity is due to altered P transport at variable segments of the proximal convoluted tubule.

Authors

G A Davidai, T Nesbitt, M K Drezner

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Total citations by year

Year: 2012 2003 2000 1999 1997 1996 1995 1994 1993 1992 1991 Total
Citations: 1 1 1 2 1 1 1 1 1 2 1 13
Citation information
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Citations to this article (13)

Title and authors Publication Year
Three novel PHEX gene mutations in four Chinese families with X-linked dominant hypophosphatemic rickets
Q Kang, J Xu, Z Zhang, J He, L Lu, W Fu, Z Zhang
Biochemical and Biophysical Research Communications 2012
Abnormal regulation of renal 25-hydroxyvitamin D-1alpha-hydroxylase activity in X-linked hypophosphatemia: a translational or post-translational defect
I Fujiwara, R Aravindan, RL Horst, MK Drezner
Journal of Bone and Mineral Research 2003
The Genetics of Osteoporosis and Metabolic Bone Disease
MJ Econs
2000
Selective decrease of mRNAs encoding plasma membrane calcium pump isoforms 2 and 3 in rat kidney
AJ Caride, EN Chini, JT Penniston, TP Dousa
Kidney International 1999
Molecular and Cellular Pediatric Endocrinology
S Handwerger
1999
Positional cloning of the PEX gene: new insights into the pathophysiology of X-linked hypophosphatemic rickets
MJ Econs, F Francis
American journal of physiology. Renal physiology 1997
Effects of altered diet on serum levels of 1,25-dihydroxyvitamin D and parathyroid hormone in X-linked hypophosphatemic (Hyp and Gy) mice
RA Meyer, MH Meyer, PL Morgan
Bone 1996
Femoral abnormalities and vitamin D metabolism in X-linked hypophosphatemic (Hyp andGy) mice
RA Meyer, MH Meyer, RW Gray, ME Bruns
Journal of Orthopaedic Research 1995
Molecular biology of hypophosphataemic rickets and oncogenic osteomalacia
PS Rowe
Human Genetics 1994
Intestinal malabsorption of45calcium in youngGymice, a second model for X-linked hypophosphatemia
JE Woodward, MH Meyer, RW Gray, RA Meyer
Journal of Bone and Mineral Research 1993
Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family
RV Thakker, MR Farmery, NA Sakatl, RD Mllner
Clinical Endocrinology 1992
Craniometric measurements of craniofacial malformations in the X-linked hypophosphatemic (Hyp) mouse on two different genetic backgrounds: C57BL/6J and B6C3H
CD Gonzalez, RA Meyer, RJ Iorio
Teratology 1992
Craniofacial abnormalities in mice with X-Linked hypophosphatemic genes (Hyp orGy)
NS Shetty, RA Meyer
Teratology 1991

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