Preconditioning is correlated with altered collagen fiber alignment in ligament.
نویسندگان
چکیده
Although the mechanical phenomena associated with preconditioning are well-established, the underlying mechanisms responsible for this behavior are still not fully understood. Using quantitative polarized light imaging, this study assessed whether preconditioning alters the collagen fiber alignment of ligament tissue, and determined whether changes in fiber organization are associated with the reduced force and stiffness observed during loading. Collagen fiber alignment maps of facet capsular ligaments (n = 8) were generated before and after 30 cycles of cyclic tensile loading, and alignment vectors were correlated between the maps to identify altered fiber organization. The change in peak force and tangent stiffness between the 1st and 30th cycle were determined from the force-displacement response, and the principal strain field of the capsular ligament after preconditioning was calculated from the fiber alignment images. The decreases in peak ligament force and tangent stiffness between the 1st and 30th cycles of preconditioning were significantly correlated (R ≥ 0.976, p < 0.0001) with the change in correlation of fiber alignment vectors between maps. Furthermore, the decrease in ligament force was correlated with a rotation of the average fiber direction toward the direction of loading (R = -0.730; p = 0.0396). Decreases in peak force during loading and changes in fiber alignment after loading were correlated (p ≤ 0.0157) with the average principal strain of the unloaded ligament after preconditioning. Through the use of a vector correlation algorithm, this study quantifies detectable changes to the internal microstructure of soft tissue produced by preconditioning and demonstrates that the reorganization of the capsular ligament's collagen fiber network, in addition to the viscoelasticity of its components, contribute to how the mechanical properties of the tissue change during its preconditioning.
منابع مشابه
Regional Changes in Collagen Fiber Alignment May Identify the Onset of Damage in the Facet Capsular Ligament
Detecting the initiation of mechanical injury of soft tissue, and not only its ultimate failure, is critical to enable a sensitive and specific characterization of tissue tolerance, to develop quantitative relationships between macroand micro-structural tissue responses, and to appropriately interpret physiological responses to loading. We have developed a novel methodological approach to detec...
متن کاملAltered collagen fiber kinematics define the onset of localized ligament damage during loading.
Detecting the initiation of mechanical injury to biological tissue, and not just its ultimate failure, is critical to a sensitive and specific characterization of tissue tolerance, development of quantitative relationships between macro- and microstructural tissue responses, and appropriate interpretation of physiological responses to loading. We have developed a novel methodological approach t...
متن کاملEffects of 2D and 3D Collagen Fiber Orientation on Ligament Fibroblast Migration
Introduction Ligament fibroblasts reside in a highly fibrous and anisotropic microenvironment. The type I collagen that made up the majority of the ligament extracellular matrix are organized into fiber bundles and crimp structures. This highly aligned arrangement has been shown to modulate fibroblast morphology, collagen expression and mechanotransduction [1]. In addition, fibroblasts exhibit ...
متن کاملFull field strain measurements of collagenous tissue by tracking fiber alignment through vector correlation.
Full field strain measurements of biological tissue during loading are often limited to the quantification of fiduciary marker displacements on the tissue surface. These marker measurements can lack the necessary spatial resolution to characterize non-uniform deformation and may not represent the deformation of the load-bearing collagen microstructure. To overcome these potential limitations, a...
متن کاملStretch-induced network reconfiguration of collagen fibres in the human facet capsular ligament.
Biomaterials can display complex spatial patterns of cellular responses to external forces. Revealing and predicting the role of these patterns in material failure require an understanding of the statistical dependencies between spatially distributed changes in a cell's local biomechanical environment, including altered collagen fibre kinematics in the extracellular matrix. Here, we develop and...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of biomechanical engineering
دوره 133 6 شماره
صفحات -
تاریخ انتشار 2011