4.5 Article

Measurements of proteoglycan and water content distribution in human lumbar intervertebral discs

Journal

SPINE
Volume 32, Issue 14, Pages 1493-1497

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/BRS.0b013e318067dd3f

Keywords

proteoglycans; aggrecan; glycosaminoglycan content; fixed charge density; intervertebral disc; degeneration

Funding

  1. NIAMS NIH HHS [R01 AR049370, R01 AR 049370, R01 AR051146] Funding Source: Medline

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Study Design. Study of regional variations in composition in a sample of 9 mildly to moderately degenerated human intervertebral discs. Objective. The aim of this study was to obtain proteoglycan distribution in human lumbar discs with high position resolution in the: 1) sagittal, 2) coronal, and 3) axial directions. Summary of Background Data. Regional variation in disc proteoglycan content has only been reported in coronal sections in a small number of discs and with low spatial resolution in the sagittal direction, and has not been reported in the axial direction. Methods. Each of 9 human L2-L3 or L3-L4 lumbar discs ( age, 53-56 years) were dissected into 36 to 41 specimens using a rectangular cutting die, measured for water content and analyzed for glycosaminoglycan content using the dimethylmethylene blue dye binding assay. Results. The intervertebral discs were mildly to moderately degenerated. They had glycosaminoglycan content ranging similar to 40 to 600 mu g/mg dry tissue, with largest values in the nucleus and lowest in the outer anulus. In general, posterior regions had greater glycosaminoglycan content than anterior regions, although values were not as high as in the nucleus. Small variations in glycosaminoglycan content in the axial direction were observed with the largest values in the center, although this variation was small compared with radial variations. Water content results followed similar trends as glycosaminoglycan content with average values ranging from similar to 66% to 86%. Conclusions. A refined map of proteoglycan content is presented with 3 important findings. First, sagittal variations were distinct from coronal variations. Second, the proteoglycan content was not uniform across the nucleus regions. Third, some specimens had localized variations in proteoglycan and water contents suggestive of focal damage and degeneration.

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