Cargando…

SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues

BACKGROUND: In vivo animal models for testing the pharmacokinetics and bioactivity of PTH and its analogues require parathyroidectomy by surgery (1, 2). As the parathyroid glands of rodents are very small the surgery often includes thyroidectomy, making this animal model time-limited, single use, co...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramezani-Pour, Narjes, Esfahani, Sayyed Hamid Zarkesh, Pradhananga, Sarbendra, Newell-Price, John D C, Ross, Richard John M, Wilkinson, Ian R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208699/
http://dx.doi.org/10.1210/jendso/bvaa046.505
_version_ 1783530907014004736
author Ramezani-Pour, Narjes
Esfahani, Sayyed Hamid Zarkesh
Pradhananga, Sarbendra
Newell-Price, John D C
Ross, Richard John M
Wilkinson, Ian R
author_facet Ramezani-Pour, Narjes
Esfahani, Sayyed Hamid Zarkesh
Pradhananga, Sarbendra
Newell-Price, John D C
Ross, Richard John M
Wilkinson, Ian R
author_sort Ramezani-Pour, Narjes
collection PubMed
description BACKGROUND: In vivo animal models for testing the pharmacokinetics and bioactivity of PTH and its analogues require parathyroidectomy by surgery (1, 2). As the parathyroid glands of rodents are very small the surgery often includes thyroidectomy, making this animal model time-limited, single use, complex, and expensive. We have developed a non-surgical rodent model of hypoparathyroidism using the Type II calcimimetic compound, Cinacalcet-HCl, to suppress PTH and thereby serum calcium levels. Methods: Normal male Wistar rats were gavaged with 30 mg/kg Cinacalcet-HCl (or vehicle only). To test the effect of PTH 1–34, animals were dosed immediately after Cinacalcet-HCl gavage with either a single subcutaneous injection of PTH at 20 nmol/kg or given as same dose repeated every hour for 6 hrs or vehicle only. Serum samples were analysed for ionised calcium (iCa) using an EasyLyte, fully automated electrolyte analyser (Medica Corporation) and phosphate using a Phosphorus Detection Assay Kit (Pars Azmun, IRAN) and an Hitachi 917 Clinical Chemistry Analyser. Results: Rats gavaged with 30 mg/kg Cinacalcet-HCl produced a significant reduction in iCa levels between 2-24hrs returning to baseline at 48-72hrs post dose with the nadir at 8 hours (ANOVA P < 0.0001). This equated to a 25% reduction in iCa at 8 hrs: mean±SD, iCa 1.19 ± 0.09 mmol/L at predose and 0.891 ± 0.04 mmol/L at 8 hours (t-test P < 0.0001). For phosphate there was an initial lowering within the first 2 hrs in all test groups but then a rise such that phosphate was at higher levels than control from 8–24 hrs (ANOVA, ns), returning to baseline at 48 hrs. PTH at 20 nmol/kg given as a single sc dose abrogated the Cinacalcet-HCl induced fall in iCa for up to 2 hrs (AUC±SD (mmol/L).hr, 0.076 ±0.047 versus 0.168±0.0874, t-test P=0.0289). Conclusions: We have shown that the administration of Cinacalcet-HCl provides a robust and reproducible lowering of calcium which is line with current published data (3). These studies demonstrate that the use of Cinacalcet-HCl in normal rats produces a hypocalcemic state that can be abrogated by the addition of PTH. This non-surgical animal model of hypoparathyroidism will be of value in testing the pharmacodynamics of PTH analogues. References 1. Shimizu M, et al. J Bone Miner Res. 2016;31(7):1405–12. 2. Jung SY, et al. PLoS One. 2016;11(10):e0163911-e. 3. Nemeth EF, et al. 2004;308(2):627–35.
format Online
Article
Text
id pubmed-7208699
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-72086992020-05-13 SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues Ramezani-Pour, Narjes Esfahani, Sayyed Hamid Zarkesh Pradhananga, Sarbendra Newell-Price, John D C Ross, Richard John M Wilkinson, Ian R J Endocr Soc Bone and Mineral Metabolism BACKGROUND: In vivo animal models for testing the pharmacokinetics and bioactivity of PTH and its analogues require parathyroidectomy by surgery (1, 2). As the parathyroid glands of rodents are very small the surgery often includes thyroidectomy, making this animal model time-limited, single use, complex, and expensive. We have developed a non-surgical rodent model of hypoparathyroidism using the Type II calcimimetic compound, Cinacalcet-HCl, to suppress PTH and thereby serum calcium levels. Methods: Normal male Wistar rats were gavaged with 30 mg/kg Cinacalcet-HCl (or vehicle only). To test the effect of PTH 1–34, animals were dosed immediately after Cinacalcet-HCl gavage with either a single subcutaneous injection of PTH at 20 nmol/kg or given as same dose repeated every hour for 6 hrs or vehicle only. Serum samples were analysed for ionised calcium (iCa) using an EasyLyte, fully automated electrolyte analyser (Medica Corporation) and phosphate using a Phosphorus Detection Assay Kit (Pars Azmun, IRAN) and an Hitachi 917 Clinical Chemistry Analyser. Results: Rats gavaged with 30 mg/kg Cinacalcet-HCl produced a significant reduction in iCa levels between 2-24hrs returning to baseline at 48-72hrs post dose with the nadir at 8 hours (ANOVA P < 0.0001). This equated to a 25% reduction in iCa at 8 hrs: mean±SD, iCa 1.19 ± 0.09 mmol/L at predose and 0.891 ± 0.04 mmol/L at 8 hours (t-test P < 0.0001). For phosphate there was an initial lowering within the first 2 hrs in all test groups but then a rise such that phosphate was at higher levels than control from 8–24 hrs (ANOVA, ns), returning to baseline at 48 hrs. PTH at 20 nmol/kg given as a single sc dose abrogated the Cinacalcet-HCl induced fall in iCa for up to 2 hrs (AUC±SD (mmol/L).hr, 0.076 ±0.047 versus 0.168±0.0874, t-test P=0.0289). Conclusions: We have shown that the administration of Cinacalcet-HCl provides a robust and reproducible lowering of calcium which is line with current published data (3). These studies demonstrate that the use of Cinacalcet-HCl in normal rats produces a hypocalcemic state that can be abrogated by the addition of PTH. This non-surgical animal model of hypoparathyroidism will be of value in testing the pharmacodynamics of PTH analogues. References 1. Shimizu M, et al. J Bone Miner Res. 2016;31(7):1405–12. 2. Jung SY, et al. PLoS One. 2016;11(10):e0163911-e. 3. Nemeth EF, et al. 2004;308(2):627–35. Oxford University Press 2020-05-08 /pmc/articles/PMC7208699/ http://dx.doi.org/10.1210/jendso/bvaa046.505 Text en © Endocrine Society 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Bone and Mineral Metabolism
Ramezani-Pour, Narjes
Esfahani, Sayyed Hamid Zarkesh
Pradhananga, Sarbendra
Newell-Price, John D C
Ross, Richard John M
Wilkinson, Ian R
SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues
title SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues
title_full SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues
title_fullStr SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues
title_full_unstemmed SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues
title_short SAT-396 A Non-Surgical Animal Model of Hypoparathyroidism for Testing PTH Analogues
title_sort sat-396 a non-surgical animal model of hypoparathyroidism for testing pth analogues
topic Bone and Mineral Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208699/
http://dx.doi.org/10.1210/jendso/bvaa046.505
work_keys_str_mv AT ramezanipournarjes sat396anonsurgicalanimalmodelofhypoparathyroidismfortestingpthanalogues
AT esfahanisayyedhamidzarkesh sat396anonsurgicalanimalmodelofhypoparathyroidismfortestingpthanalogues
AT pradhanangasarbendra sat396anonsurgicalanimalmodelofhypoparathyroidismfortestingpthanalogues
AT newellpricejohndc sat396anonsurgicalanimalmodelofhypoparathyroidismfortestingpthanalogues
AT rossrichardjohnm sat396anonsurgicalanimalmodelofhypoparathyroidismfortestingpthanalogues
AT wilkinsonianr sat396anonsurgicalanimalmodelofhypoparathyroidismfortestingpthanalogues