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

JOR Spine ◽  
2021 ◽  
Author(s):  
Tetsutaro Abe ◽  
Masashi Miyazaki ◽  
Toshinobu Ishihara ◽  
Shozo Kanezaki ◽  
Yuhta Tsubouchi ◽  
...  
Keyword(s):  
Parathyroid Hormone ◽  
Bone Formation ◽  
Spinal Fusion ◽  
Bone Morphogenetic Protein ◽  
Fusion Model ◽  
Intermittent Administration ◽  
Morphogenetic Protein ◽  
Administration Interval

scholarly journals Enhancing the effects of exfoliated carbon nanofibers using bone morphogenetic protein in a rat spinal fusion model

2018 ◽  
Vol 36 (11) ◽  
pp. 2892-2900
Author(s):  
Naoki Notani ◽  
Masashi Miyazaki ◽  
Masahiro Toyoda ◽  
Shozo Kanezaki ◽  
Toshinobu Ishihara ◽  
...  
Keyword(s):  
Spinal Fusion ◽  
Bone Morphogenetic Protein ◽  
Carbon Nanofibers ◽  
Fusion Model ◽  
Morphogenetic Protein

scholarly journals Enhanced Bone Morphogenetic Protein-2-Induced Ectopic and Orthotopic Bone Formation by Intermittent Parathyroid Hormone (1–34) Administration

2010 ◽  
Vol 16 (12) ◽  
pp. 3769-3777 ◽  
Author(s):  
Diederik H.R. Kempen ◽  
Lichun Lu ◽  
Theresa E. Hefferan ◽  
Laura B. Creemers ◽  
Andras Heijink ◽  
...  
Keyword(s):  
Parathyroid Hormone ◽  
Bone Formation ◽  
Bone Morphogenetic Protein ◽  
Bone Morphogenetic Protein 2 ◽  
Morphogenetic Protein

Bone morphogenetic protein gene therapy for the induction of spinal arthrodesis

1998 ◽  
Vol 4 (2) ◽  
pp. E14 ◽  
Author(s):  
Tord D. Alden ◽  
Gerald R. Hankins ◽  
Elisa J. Beres ◽  
David F. Kallmes ◽  
Gregory A. Helm
Keyword(s):  
Gene Therapy ◽  
Bone Formation ◽  
Spinal Fusion ◽  
Bone Morphogenetic Protein ◽  
Bone Morphogenetic Protein 2 ◽  
Lumbosacral Spine ◽  
Ct Reconstruction ◽  
Morphogenetic Protein ◽  
Adenoviral Construct

Gene therapy has many potential applications in neurosurgery. One application involves bone morphogenetic protein-2 (BMP-2), a low-molecular-weight glycoprotein that induces bone formation in vivo. Numerous studies have demonstrated that the BMP-2 protein can enhance spinal fusion. This study was undertaken to determine whether direct injection of an adenoviral construct containing the BMP-2 gene can be used for spinal fusion. Twelve athymic nude rats were used in this study. Recombinant, replication-defective type-5 adenovirus with a universal promoter and BMP-2 gene (Ad-BMP-2) was used. A second adenovirus constructed with a universal promoter and ß-galactosidase (ß-gal) gene (Ad-ß-gal) was used as a control. Seven and one-half microliters of virus was injected percutaneously and paraspinally at the lumbosacral junction in three groups (four animals each): 1) Ad-BMP-2 bilaterally, 2) Ad-BMP-2 on the right, Ad-ß-gal on the left, and 3) Ad-ß-gal bilaterally. Computerized tomography (CT) scans of the lumbosacral spine were obtained at 3, 5, and 12 weeks. At 12 weeks, the animals were killed for histological inspection. Ectopic bone formation was seen both on three-dimensional CT reconstruction and histologically in all rats at sites treated with Ad-BMP-2. Histological analysis revealed bone at different stages of maturity adjacent to the spinous processes, laminae, and transverse processes. This study clearly demonstrated that it is possible to produce in vivo endochondral bone formation by using direct adenoviral construct injection into the paraspinal musculature, which suggests that gene therapy may be useful for spinal fusion in the future.

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