摘要

Objective: The objective of this study was to evaluate the feasibility of quantifying the Equilibrium Partitioning of an Ionic Contrast agent via Microcomputed Tomography (EPIC-mu CT) to nondestructively assess sulfated glycosaminoglycan (sGAG) content and distribution in rat articular cartilage ex vivo, and in doing so to establish a paradigm for extension of this technique to other small animal models. Design: After determination of an appropriate incubation time for the anionic contrast agent, EPIC-mu CT was used to examine age-related differences in cartilage sGAG content between 4-, 8-, and 16-week old (n = 5 each) male Wistar rats and to evaluate sGAG depletion in the right femora of each age group after 60 min of digestion with chondroitinase ABC. The EPIC-mu CT measurements were validated by histological safranin-O staining, and reproducibility was evaluated by triplicate scans of six femora. Results: Cartilage attenuation gradually increased with cumulative digestion time and reached a plateau at approximately 60 min with a 16.0% temporal increase (P < 0.01). Average femoral articular cartilage attenuation increased by 14.2% from 4- to 8-weeks of age (P < 0.01) and further increased by 2.5% from 8 to 16 weeks (P < 0.05). After 60 min of digestion, femoral articular cartilage attenuations increased by 15-17% in each age group (P < 0.01). Correspondingly, sGAG optical density decreased with age and digestion, and showed a linear correlation (r=-0.88, slope=-1.26, P<0.01, n=30) with EPIC-mu CT cartilage attenuation. High reproducibility was indicated by a low coefficient of variation (1.5%) in cartilage attenuation. Conclusions: EPIC-mu CT imaging provides high spatial resolution and sensitivity to assess sGAG content and three-dimensional distribution in rat femoral articular cartilage.

  • 出版日期2010-1