PMID- 26381618 OWN - NLM STAT- MEDLINE DCOM- 20161005 LR - 20211203 IS - 1422-6421 (Electronic) IS - 1422-6405 (Print) IS - 1422-6405 (Linking) VI - 200 IP - 6 DP - 2015 TI - Fluoride Modulates Parathyroid Hormone Secretion in vivo and in vitro. PG - 413-23 LID - 10.1159/000438699 [doi] AB - The study objective was to investigate the effects of fluoride on intact parathyroid hormone (iPTH) secretion. Thyro-parathyroid complexes (TPC) from C3H (n = 18) and B6 (n = 18) mice were cultured in Ca(2)(+)-optimized medium. TPC were treated with 0, 250, or 500 microM NaF for 24 h and secreted iPTH assayed by ELISA. C3H (n = 78) and B6 (n = 78) mice were gavaged once with distilled or fluoride (0.001 mg [F(-)]/g of body weight) water. At serial time points (0.5-96 h) serum iPTH, fluoride, total calcium, phosphorus, and magnesium levels were determined. Expression of genes involved in mineral regulation via the bone-parathyroid-kidney (BPK) axis, such as parathyroid hormone (Pth), calcium-sensing receptor (Casr), vitamin D receptor (Vdr), parathyroid hormone-like hormone (Pthlh), fibroblast growth factor 23 (Fgf23), alpha-Klotho (alphaKlotho), fibroblast growth factor receptor 1c (Fgf1rc), tumor necrosis factor 11 (Tnfs11), parathyroid hormone receptor 1 (Pth1r), solute carrier family 34 member 1 (Slc34a1), solute carrier 9 member 3 regulator 1 (Slc9a3r1), chloride channel 5 (Clcn5), and PDZ domain-containing 1 (Pdzk1), was determined in TPC, humeri, and kidneys at 24 h. An in vitro decrease in iPTH was seen in C3H and B6 TPC at 500 microM (p < 0.001). In vivo levels of serum fluoride peaked at 0.5 h in both C3H (p = 0.002) and B6 (p = 0.01). In C3H, iPTH decreased at 24 h (p < 0.0001), returning to baseline at 48 h. In B6, iPTH increased at 12 h (p < 0.001), returning to baseline at 24 h. Serum total calcium, phosphorus, and magnesium levels did not change significantly. Pth, Casr,alphaKlotho,Fgf1rc,Vdr, and Pthlh were significantly upregulated in C3H TPC compared to B6. In conclusion, the effects of fluoride on TPC in vitro were equivalent between the 2 mouse strains. However, fluoride demonstrated an early strain-dependent effect on iPTH secretion in vivo. Both strains demonstrated differences in the expression of genes involved in the BPK axis, suggesting a possible role in the physiologic handling of fluoride. CI - (c) 2015 S. Karger AG, Basel. FAU - Puranik, Chaitanya P AU - Puranik CP AD - Oral Biology PhD Curriculum, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, N.C., USA. FAU - Ryan, Kathleen A AU - Ryan KA FAU - Yin, Zhaoyu AU - Yin Z FAU - Martinez-Mier, E Angeles AU - Martinez-Mier EA FAU - Preisser, John S AU - Preisser JS FAU - Everett, Eric T AU - Everett ET LA - eng GR - R01 DE018104/DE/NIDCR NIH HHS/United States GR - R01DE018104/DE/NIDCR NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20150919 PL - Switzerland TA - Cells Tissues Organs JT - Cells, tissues, organs JID - 100883360 RN - 0 (Fgf23 protein, mouse) RN - 0 (Parathyroid Hormone) RN - 27YLU75U4W (Phosphorus) RN - 7Q7P4S7RRE (Fibroblast Growth Factor-23) RN - 8ZYQ1474W7 (Sodium Fluoride) RN - I38ZP9992A (Magnesium) RN - SY7Q814VUP (Calcium) SB - IM MH - Animals MH - Calcium/blood MH - Cells, Cultured MH - Fibroblast Growth Factor-23 MH - Gene Expression Regulation/drug effects MH - Magnesium/blood MH - Male MH - Mice, Inbred C3H MH - Mice, Inbred C57BL MH - Parathyroid Glands/cytology/drug effects/metabolism MH - Parathyroid Hormone/*blood/metabolism MH - Phosphorus/blood MH - Sodium Fluoride/administration & dosage/blood/*pharmacology PMC - PMC4679577 MID - NIHMS708704 COIS- Conflicts of interest The authors do not have any conflicts of interest. EDAT- 2015/09/19 06:00 MHDA- 2016/10/07 06:00 PMCR- 2016/12/01 CRDT- 2015/09/19 06:00 PHST- 2015/07/14 00:00 [accepted] PHST- 2015/09/19 06:00 [entrez] PHST- 2015/09/19 06:00 [pubmed] PHST- 2016/10/07 06:00 [medline] PHST- 2016/12/01 00:00 [pmc-release] AID - 000438699 [pii] AID - 10.1159/000438699 [doi] PST - ppublish SO - Cells Tissues Organs. 2015;200(6):413-23. doi: 10.1159/000438699. Epub 2015 Sep 19.