To clarify the early process of recovery at the bone-tendon interface, we used light microscopy and SEM to examine the process of anchoring of collagen fibers to bone in a canine model.At two weeks, tendon, scar tissue, woven bone and lamellar bone were present at the insertion site. SEM revealed anchoring of collagen fibril bundles of the scar to the woven bone. By 4 weeks, the number of anchoring fibers had increased and a parallel arrangement of fibers was observed. SEM demonstrated deep penetration of fibers into the woven bone layer. In addition, the fibers were observed to project into and intermingle with the scar tissue. By 6 weeks, the anchoring fibers had developed fully and were distributed densely over the interface. SEM also revealed that the collagen fibril bundles in the scar tissue had connected with the collagen fibrils of the woven bone by way of the anchoring bundles. The woven bone was identifiable throughout the early stages of recovery as the interface between soft tissue and hard tissue. Throughout all experimental periods, no staining was observed at the interface of the tendon and bone by Saffranin-0. The formation of woven bone was important during early recovery of the tendonbone interface prior to the completion of fibrocartilage-mediated insertion. 0
Summary: Using 10 osteoligamentous vertebral columns obtained from elderly donated cadavers, we describe in detail degenerative changes of the articular cartilage in lumbar zygapophysial joints to show which portion in a facet is specifically affected. Degenerative changes, including extended cartilage defects, occurred in multiple facets of every specimen. The results demonstrated 5 basic morphologies of degeneration, i.e., 1) marginal dominace in the articular surface, 2) lower segment dominance except for the lowest (L5/S) facet, 3) advancement in the inferior articular process, 4) cranial and caudal dominance rather than the dorsal dominance in the articular surface and 5) progress in a mirror-image manner. These rules seemed to be consistent with differences in size, shape and kinesiological aspects of the facet between segments and between portions in a facet.
Using 26 osteoligamentous lumbar vertebral columns (260 facets), we morphometrically investigated the cartilagenous joint surface, inner capsular surface and capsular thickness. We also examined whether the subcapsular pocket was present and, if present, how far it extended along the joint margin. The proportion of the inner capsular area in the total joint surface area in a facet (the capsular-joint surface ratio) was hypothesized to correspond to the potential looseness (or tightness) of the facet. The absolute data themselves seemed to be useful for better understanding of the joint morphology. However, further evaluations of the differences between segments, left/right differences, individual segmental fluctuation patterns and correlations between parameters provided a novel classification of specimens according to the hypothetical progress of joint degeneration. Criteria for the classification existed in 1) the laterality in parameters defined as more than 100% larger or smaller than the contralateral facet and 2) the drastic segmental difference in parameters over 50% larger or smaller than the adjacent segment. Consequently, three types were identified: 1) outside of the criteria in both area and thickness (-/- type, 9 of 26); 2) the criteria did not fit the area parameters but did fit the thickness parameters (-/+ type, 8); the criteria were filled in both categories of parameters (+/+ type, 9). Notably, in the +/+ types, the capsular thickness and capsular-joint surface ratio correlated significantly (p < 0.01), i.e., the hypothetical loose joint had a thick capsule. We speculated that early joint degeneration starts from the -/- type and advances via the -/+ type to the +/+ type. Considerating these results, we recommended using MR imaging for detailed identification of laterality in the capsular thickness for low-back pain patients to discriminate candidates for future severe degenerative changes of the articular cartilage in the lumbar spine.
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