The effect of bone morphogenetic protein-2 injection at different time points on intervertebral disk degeneration in a rat tail model

J Spinal Disord Tech. 2015 Feb;28(1):E35-44. doi: 10.1097/BSD.0000000000000141.

Abstract

Study design: Prospective in vivo rat tail model of disk degeneration comparing the effects of recombinant human bone morphogenetic protein-2 (rhBMP-2) injection over various time points and grades of degeneration.

Objective: To evaluate the effect of timing and disk grade on rhBMP-2 injection in a rat tail model of disk degeneration.

Summary of background data: rhBMP-2 stimulates the proliferation of intervertebral disk cells and the secretion of extracellular matrix. However, few in vivo studies have demonstrated whether rhBMP-2 also improves disk degeneration and the severity of disk degeneration beyond which disks cannot be recovered by rhBMP-2 treatment.

Methods: Two coccygeal disks of each rodent subject were punctured percutaneously using an 18 G needle. At 4 weeks after the puncture, disks demonstrating induced degeneration were divided into 3 groups. Groups 1, 2, and 3 were treated with 7.5 μg rhBMP-2 or phosphate buffered saline by injection into the disk at 4, 6, and 8 weeks postpuncture, respectively. Plain radiographs and magnetic resonance images (MRIs) were obtained on the day of puncture and every 2 weeks thereafter until sacrifice. At 6 weeks after injection, each group was killed and examined with histologic and immunohistochemical analysis.

Results: According to MRI disk grade evaluation of the degenerative disk, rhBMP-2 significantly improved degeneration grade in group 1 at 2 weeks after injection. According to radiographic disk height index, groups 1 and 2 showed a trend toward improvement at 2 weeks after rhBMP-2 injection. Chondrogenic differentiation was noted on immunohistochemical staining of many disks treated with rhBMP-2.

Conclusions: rhBMP-2 injection of degenerated disks at 4 weeks postpuncture induced a transient improvement in disk grade on MRI and stimulated chondrogenic differentiation. These data suggest rhBMP-2 as a potential therapy for degenerative disk disease.

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 2 / administration & dosage*
  • Bone Morphogenetic Protein 2 / pharmacology
  • Bone Morphogenetic Protein 2 / therapeutic use*
  • Disease Models, Animal
  • Humans
  • Immunohistochemistry
  • Injections
  • Intervertebral Disc / drug effects
  • Intervertebral Disc / pathology
  • Intervertebral Disc Degeneration / diagnostic imaging
  • Intervertebral Disc Degeneration / drug therapy*
  • Intervertebral Disc Degeneration / pathology
  • Magnetic Resonance Imaging
  • Male
  • Prospective Studies
  • Proteoglycans / metabolism
  • Punctures
  • Radiography
  • Rats, Inbred Lew
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / pharmacology
  • Recombinant Proteins / therapeutic use
  • Staining and Labeling
  • Tail / drug effects*
  • Time Factors
  • Transforming Growth Factor beta / administration & dosage*
  • Transforming Growth Factor beta / pharmacology
  • Transforming Growth Factor beta / therapeutic use*

Substances

  • Bone Morphogenetic Protein 2
  • Proteoglycans
  • Recombinant Proteins
  • Transforming Growth Factor beta
  • recombinant human bone morphogenetic protein-2