On the anisotropy of the canine diaphragmatic central tendon.

We studied the mechanical and anatomical anisotropy of the canine diaphragmatic central tendon (CT). Dumb-bell-shaped strips with effective dimensions of 10 x 2 mm (length x width) were cut from different regions of the canine diaphragmatic CT in two different orientations relative to the direction of neighboring muscle fibers. Specimens sampled with their long axial dimension oriented parallel to the neighboring muscle fibers were named Group-1 and those sampled with an orientation perpendicular to the neighboring muscle fibers were named Group-2. Results from one-dimensional stress-strain and tensile failure strength tests revealed that the CT is a nonlinear, inelastic, and anisotropic material. Group-1 specimens were found to have a higher stiffness, higher failure strength and higher strain energy density at failure than Group-2 specimens. Polarized microscopy showed that multiple sheets of collagen fiber bundles formed an orthogonal network in the tendon. Collagen fiber bundles along Group-1 direction formed parallel trajectory lines connecting the neighboring costal and crural muscles; bundles along Group-2 direction were observed to orient 90 degrees away. At the central apex region of the CT, collagen bundles of Group-1 formed a fan-like trajectory pattern. This collagen network architecture was compared favorably to the trajectories of an approximated principal stress field in the CT due to simulated contractile forces from its adjacent costal and crural muscles. These combined results suggest a structure-function relationship for the anatomical and mechanical anisotropy in the canine diaphragmatic CT.

[1]  R. Haut The effect of a lathyritic diet on the sensitivity of tendon to strain rate. , 1985, Journal of biomechanical engineering.

[2]  George C. Derringer Statistics for the engineering and computer sciences , 1984 .

[3]  J. Sharp,et al.  Mechanics of the canine diaphragm. , 1976, Journal of applied physiology.

[4]  A. Foux,et al.  Physico-chemical and microstructural changes in collagen fiber bundles following stretch in-vitro. , 1988, Biorheology.

[5]  S. Rodbard Negative Feedback Mechanisms in the Architecture and Function of the Connective and Cardiovascular Tissues , 2015, Perspectives in biology and medicine.

[6]  P. Macklem,et al.  The respiratory muscles. , 1982, The New England journal of medicine.

[7]  F. Noyes,et al.  Effects of structure and strain measurement technique on the material properties of young human tendons and fascia. , 1984, Journal of biomechanics.

[8]  G. Piérard,et al.  Microanatomy of the dermis in relation to relaxed skin tension lines and Langer's lines. , 1987, The American Journal of dermatopathology.

[9]  P. Macklem,et al.  The diaphragm: two muscles. , 1981, Science.

[10]  J. Z. Zhu,et al.  The finite element method , 1977 .

[11]  D. F. Rochester,et al.  Functional characteristics of canine costal and crural diaphragm. , 1988, Journal of applied physiology.

[12]  Frank C. P. Yin,et al.  A Video-Dimension Analyzer , 1972 .

[13]  S. Woo,et al.  Biomechanics of Tendons and Ligaments , 1986 .

[14]  L. Buja,et al.  Glycol Methacrylate for Histology: Problems and Solutions , 1984 .

[15]  D M Blair,et al.  A Study of the Central Tendon of the Diaphragm. , 1923, Journal of anatomy.

[16]  Y. Fung,et al.  Biomechanics: Mechanical Properties of Living Tissues , 1981 .

[17]  A Viidik,et al.  Changes in tensile strength characteristics and histology of rabbit ligaments induced by different modes of postmortal storage. , 1966, Acta orthopaedica Scandinavica.