Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7659
Title: Local rhBMP-2 injection after drill-hole injury in rats: Does it have systemic effects?
Authors: Demirkan, Neşe
Demirkan, Ahmet Fahir
Aksoy, A.
Özdemir, M.
Akman, A.
Keywords: Bone morphogenic protein
Callus
Fracture
Parathyroid hormone
ß-catenin
beta catenin
bone morphogenic protein 2 antibody
parathyroid hormone
protein antibody
recombinant bone morphogenetic protein 2
transcription factor 7 like 2
unclassified drug
water
bone morphogenetic protein 4
animal cell
animal experiment
animal model
animal tissue
article
callus
cartilage cell
controlled study
femoral drill hole injury
femur
femur fracture
fibroblast
histopathology
immunohistochemistry
Kirschner wire
male
mesenchyme cell
molecular interaction
nonhuman
ossification
osteoblast
osteoclast
osteocyte
periosteum
priority journal
protein expression
rat
Article
bone drill
in vivo study
protein protein interaction
Animals
beta Catenin
Bone Morphogenetic Protein 2
Bone Remodeling
Disease Models, Animal
DNA-Binding Proteins
Femoral Fractures
Femur
Fracture Healing
Injections
Male
Parathyroid Hormone
Rats
Rats, Sprague-Dawley
Recombinant Proteins
Signal Transduction
Time Factors
Transcription Factors
Publisher: Biolife s.a.s.
Abstract: The aim of this study is to investigate the histopathological findings of drill hole healing and interactions of parathyroid hormone (PTH), ß-catenin and transcription factor-4 (TCF7L2/Tcf-4) after local application of recombinant human bone morphogenic protein-2 (rhBMP-2). Sprague Dawley rats were used in two groups of 'femoral cortex hole model'. In the non-treated group, a hole was opened with a 3 mm K-wire in the distal and mid third junction of the right femur. In the treated group, local rhBMP-2 protein was injected into the similar femoral hole. Sterile 18M H2O was injected into the femoral hole at contralateral femur. There was more subperiosteal membranous bone reaction in the group treated with rhBMP-2 injection compared to the non-treated group. This was also proven immunohistochemically in both ipsilateral and contralateral femur with increased anti bone morphogenic protein-2 (anti BMP-2) expression. Moreover, there was an increased subperiosteal reaction at the contralateral femur. Also, in the treated group, PTH expression was increased in cells that form callus, and nuclear beta-catenin expression was increased in chondrocytes of periosteal ossification. Future studies should try to find whether the effects of rhBMP-2 on PTH and Wnt signaling pathway changes with different fracture models, also the systemic effects of local rhBMP-2 application should be investigated. Copyright © by BIOLIFE, s.a.s.
URI: https://hdl.handle.net/11499/7659
https://doi.org/10.1177/039463201402700212
ISSN: 0394-6320
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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