Cargando…

Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model

INTRODUCTION: Both bone morphogenetic protein 2 (BMP‐2) and teriparatide (parathyroid hormone [PTH] 1‐34) are used to enhance bone healing. There is still no established opinion regarding the optimum dose and administration method. We investigated the optimal administration method for the combinatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Abe, Tetsutaro, Miyazaki, Masashi, Ishihara, Toshinobu, Kanezaki, Shozo, Tsubouchi, Yuhta, Tsumura, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479526/
https://www.ncbi.nlm.nih.gov/pubmed/34611590
http://dx.doi.org/10.1002/jsp2.1168
_version_ 1784576277545484288
author Abe, Tetsutaro
Miyazaki, Masashi
Ishihara, Toshinobu
Kanezaki, Shozo
Tsubouchi, Yuhta
Tsumura, Hiroshi
author_facet Abe, Tetsutaro
Miyazaki, Masashi
Ishihara, Toshinobu
Kanezaki, Shozo
Tsubouchi, Yuhta
Tsumura, Hiroshi
author_sort Abe, Tetsutaro
collection PubMed
description INTRODUCTION: Both bone morphogenetic protein 2 (BMP‐2) and teriparatide (parathyroid hormone [PTH] 1‐34) are used to enhance bone healing. There is still no established opinion regarding the optimum dose and administration method. We investigated the optimal administration method for the combination of BMP‐2 and PTH 1‐34 in a rat spinal fusion model. METHODS: Group I was implanted with a control carrier. Groups II, III, and IV were implanted with a carrier containing 3 μg of recombinant human BMP‐2 (rhBMP‐2). In addition, following implantation, PTH 1‐34 injections were administered to Group III thrice a week (total, 180 μg/kg/week) and Group IV six times a week (total, 180 μg/kg/week). The rats were euthanized after 8 weeks, and their spines were explanted; assessed by manual palpation, radiographs, and high‐resolution micro‐computed tomography (micro‐CT); and subjected to histological analysis. Serum markers of bone metabolism were also analyzed. RESULTS: Manual palpation tests showed that the fusion rates in Groups III and IV were considerably higher than those in Group I. They also had higher radiographic scores than Group I and II. Micro‐CT analysis revealed Tb.Th in the Group IV had higher values than that in the Group I, II, III with significant differences and Tb.Sp in the Group IV had lower values than that in the Group I, II, III with significant differences. Serum marker analysis revealed that Group IV had higher osteocalcin and lower tartrate‐resistant acid phosphatase‐5b than Group III. Histological analysis indicated that Group IV had enhanced trabecular bone structure. CONCLUSIONS: Frequent administration of PTH may be better in making thicker and strengthening the trabecular bone structure in newly formed bone in the rat spinal fusion model using insufficient BMP‐2.
format Online
Article
Text
id pubmed-8479526
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-84795262021-10-04 Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model Abe, Tetsutaro Miyazaki, Masashi Ishihara, Toshinobu Kanezaki, Shozo Tsubouchi, Yuhta Tsumura, Hiroshi JOR Spine Research Articles INTRODUCTION: Both bone morphogenetic protein 2 (BMP‐2) and teriparatide (parathyroid hormone [PTH] 1‐34) are used to enhance bone healing. There is still no established opinion regarding the optimum dose and administration method. We investigated the optimal administration method for the combination of BMP‐2 and PTH 1‐34 in a rat spinal fusion model. METHODS: Group I was implanted with a control carrier. Groups II, III, and IV were implanted with a carrier containing 3 μg of recombinant human BMP‐2 (rhBMP‐2). In addition, following implantation, PTH 1‐34 injections were administered to Group III thrice a week (total, 180 μg/kg/week) and Group IV six times a week (total, 180 μg/kg/week). The rats were euthanized after 8 weeks, and their spines were explanted; assessed by manual palpation, radiographs, and high‐resolution micro‐computed tomography (micro‐CT); and subjected to histological analysis. Serum markers of bone metabolism were also analyzed. RESULTS: Manual palpation tests showed that the fusion rates in Groups III and IV were considerably higher than those in Group I. They also had higher radiographic scores than Group I and II. Micro‐CT analysis revealed Tb.Th in the Group IV had higher values than that in the Group I, II, III with significant differences and Tb.Sp in the Group IV had lower values than that in the Group I, II, III with significant differences. Serum marker analysis revealed that Group IV had higher osteocalcin and lower tartrate‐resistant acid phosphatase‐5b than Group III. Histological analysis indicated that Group IV had enhanced trabecular bone structure. CONCLUSIONS: Frequent administration of PTH may be better in making thicker and strengthening the trabecular bone structure in newly formed bone in the rat spinal fusion model using insufficient BMP‐2. John Wiley & Sons, Inc. 2021-08-18 /pmc/articles/PMC8479526/ /pubmed/34611590 http://dx.doi.org/10.1002/jsp2.1168 Text en © 2021 The Authors. JOR Spine published by Wiley Periodicals LLC on behalf of Orthopaedic Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Abe, Tetsutaro
Miyazaki, Masashi
Ishihara, Toshinobu
Kanezaki, Shozo
Tsubouchi, Yuhta
Tsumura, Hiroshi
Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model
title Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model
title_full Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model
title_fullStr Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model
title_full_unstemmed Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model
title_short Optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model
title_sort optimal intermittent administration interval of parathyroid hormone 1‐34 for bone morphogenetic protein‐induced bone formation in a rat spinal fusion model
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479526/
https://www.ncbi.nlm.nih.gov/pubmed/34611590
http://dx.doi.org/10.1002/jsp2.1168
work_keys_str_mv AT abetetsutaro optimalintermittentadministrationintervalofparathyroidhormone134forbonemorphogeneticproteininducedboneformationinaratspinalfusionmodel
AT miyazakimasashi optimalintermittentadministrationintervalofparathyroidhormone134forbonemorphogeneticproteininducedboneformationinaratspinalfusionmodel
AT ishiharatoshinobu optimalintermittentadministrationintervalofparathyroidhormone134forbonemorphogeneticproteininducedboneformationinaratspinalfusionmodel
AT kanezakishozo optimalintermittentadministrationintervalofparathyroidhormone134forbonemorphogeneticproteininducedboneformationinaratspinalfusionmodel
AT tsubouchiyuhta optimalintermittentadministrationintervalofparathyroidhormone134forbonemorphogeneticproteininducedboneformationinaratspinalfusionmodel
AT tsumurahiroshi optimalintermittentadministrationintervalofparathyroidhormone134forbonemorphogeneticproteininducedboneformationinaratspinalfusionmodel