Document Type
Article
Language
Eng
Publication Date
12-2017
Publisher
Elsevier
Source Publication
The Spine Journal
Source ISSN
1529-9430
Abstract
Background Context
Adipokines are secreted by white adipose tissue and have been associated with fracture healing. Our goal was to report the temporal expression of adipokines during spinal fusion in an established rabbit model.
Purpose
Our goal was to report the temporal expression of adipokines during spinal fusion in an established rabbit model.
Study Design
The study design included a laboratory animal model.
Methods
New Zealand white rabbits were assigned to either sham surgery (n=2), unilateral posterior spinal fusion (n=14), or bilateral posterior spinal fusion (n=14). Rabbits were euthanized 1–6 and 10 weeks out from surgery. Fusion was evaluated by radiographs, manual palpation, and histology. Reverse transcription-polymerase chain reaction on the bone fusion mass catalogued the gene expression of leptin, adiponectin, resistin, and vascular endothelial growth factor (VEGF) at each time point. Results were normalized to the internal control gene, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (2^ΔCt), and control bone sites (2^ΔΔCt). Quantitative data were analyzed by two-factor analysis of variance (p<.05).
Results
Manual palpation scores, radiograph scores, and histologic findings showed progression of boney fusion over time (p
Conclusions
Leptin expression is likely associated with the maturation phase of bone fusion. Adiponectin and resistin may play a role early on during the fusion process. Our results suggest that leptin expression may be upstream of VEGF expression during spinal fusion, and both appear to play an important role in bone spinal fusion.
Recommended Citation
Virk, Sohrab; Bertone, Alicia L.; Hussein, Hayam Hamaz; Toth, Jeffrey M.; Kaido, Mari; and Khan, Safdar, "The Temporal Expression of Adipokines During Spinal Fusion" (2017). Biomedical Engineering Faculty Research and Publications. 516.
https://epublications.marquette.edu/bioengin_fac/516
ADA accessible version
Comments
Accepted version. The Spine Journal, Vol. 17, No. 12 (December 2017): 1897-1906. DOI. © 2017 Elsevier B.V. Used with permission.