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      Fluoride Modulates Parathyroid Hormone Secretion In Vivo and In Vitro

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          Abstract

          The study objective was to investigate fluoride’s effects on iPTH secretion. Thryo-parathyroid complexes (TPCs) from C3H (n=18) and B6 (n=18) mice were cultured in Ca2+ optimized medium. TPCs were treated with 0, 250 or 500µM NaF for 24hrs and secreted iPTH assayed by ELISA. C3H (n=78) and B6 (n=78) mice were gavaged once with distilled or with fluoride (0.001mg [F ]/g body weight) water. At serial time points (0.5–96hrs) serum iPTH, fluoride, total calcium, phosphorus and magnesium levels were determined. Expression of genes involved in mineral regulation via bone-parathyroid-kidney (BPK) axis such as: Pth, Casr, Vdr, Pthlh, Fgf23, αKlotho, Fgf1rc, Tnfs11, Pth1r, Slc34a1, Slc9a3r1, Clcn5 and Pdzk1 were determined in TPCs, humerii and kidneys at 24hrs. An in vitro decrease in iPTH was seen in C3H and B6 TPC at 500µM ( p<0.001). In vivo levels of serum fluoride peaked at 0.5hr in both C3H ( p=0.002) and B6 ( p=0.01). In C3H, iPTH decreased at 24hrs ( p<0.0001) returning to baseline at 48hrs. In B6, iPTH increased at 12hrs ( p<0.001) returning to baseline at 24hrs. Serum total calcium, phosphorus and magnesium did not change significantly. Pth, Casr, αKlotho, Fgf1rc, Vdr and Pthlh were significantly up-regulated in C3H TPC as compared to B6. Conclusions, fluoride’s effects on TPC in vitro were equivalent between the two mouse strains. However, fluoride demonstrated an early strain dependent effect on iPTH secretion in vivo. Both strains demonstrated a differences in the expression of genes involved in BPK axis suggesting a possible role in physiologic handling of fluoride.

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          Author and article information

          Contributors
          Journal
          100883360
          21387
          Cells Tissues Organs
          Cells Tissues Organs (Print)
          Cells, tissues, organs
          1422-6405
          1422-6421
          25 September 2015
          19 September 2015
          December 2015
          01 December 2016
          : 200
          : 6
          : 413-423
          Affiliations
          [a ]Oral Biology PhD Curriculum, University of North Carolina at Chapel Hill
          [b ]Dental Research, University of North Carolina at Chapel Hill
          [c ]Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill
          [d ]Department of Preventive and Community Dentistry, Indiana University School of Dentistry
          [e ]Department of Pediatric Dentistry, Carolina Center for Genome Sciences, University of North Carolina at Chapel Hill
          Author notes
          Correspondence to: Eric T. Everett, Ph.D., School of Dentistry, Koury Oral Health Sciences Building, Room 4417 CB# 7455, 385 South Columbia Street, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7455, Phone: 919-537-3182, Fax: +1 919 966-3633
          Article
          PMC4679577 PMC4679577 4679577 nihpa708704
          10.1159/000438699
          4679577
          26381618
          bdf333ea-f826-4198-b2c3-2e898008beff
          History
          Categories
          Article

          bone,inbred mouse strains,parathyroid hormone,skeletal fluorosis,fluoride

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