Quantitative magnetic resonance imaging of enzymatically induced degradation of the nucleus pulposus of intervertebral discs

Spine (Phila Pa 1976). 2006 Jun 15;31(14):1547-54. doi: 10.1097/01.brs.0000221995.77177.9d.

Abstract

Study design: The structural integrity of the nucleus pulposus (NP) of intervertebral discs was targeted by enzyme-specific degradations to correlate their effects to the magnetic resonance (MR) signal.

Objective: To develop quantitative MR imaging as an accurate and noninvasive diagnostic tool to better understand and treat disc degeneration.

Summary of background data: Quantitative MR analysis has been previously shown to reflect not only the disc matrix composition, but also the structural integrity of the disc matrix. Further work is required to identify the contribution of the structural integrity versus the matrix composition to the MR signal.

Methods: The bovine coccygeal NPs were injected with either enzyme or buffer, incubated at 37 degrees C as static, unloaded and closed 3-disc segments, and analyzed by a 1.5-Tesla MR scanner to measure MR parameters.

Results: Collagenase degradation of the NP significantly decreased the relaxation times, slightly decreased the magnetization transfer ratio, and slightly increased the apparent diffusion coefficient. Targeting the proteoglycan and/or hyaluronan integrity by trypsin and hyaluronidase did not significantly affect the MR parameters, except for an increase in the apparent diffusion coefficient of the disc after trypsin treatment.

Conclusions: Our results demonstrate that changes in the structural integrity of matrix proteins can be assessed by quantitative MR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Collagen / metabolism
  • Collagenases / pharmacology
  • Hyaluronic Acid / metabolism
  • Hyaluronoglucosaminidase / drug effects
  • Intervertebral Disc / drug effects
  • Intervertebral Disc / metabolism
  • Intervertebral Disc / pathology*
  • Intervertebral Disc Chemolysis*
  • Magnetic Resonance Imaging*
  • Protein Denaturation
  • Proteoglycans / metabolism
  • Trypsin / pharmacology

Substances

  • Proteoglycans
  • Hyaluronic Acid
  • Collagen
  • Hyaluronoglucosaminidase
  • Trypsin
  • Collagenases