Strain Rate Sensitivity of Rabbit Tendon
The ultrastructural mechanism for strain rate sensitivity of collagenous tissue has not been well studied at the collagen ﬁbril level. Our objective is to reveal the mechanistic contribution of tendon’s key structural component to strain rate sensitivity. We have investigated the structure of the collagen ﬁbril undergoing tension at different strain rates. Tendon fascicles were pulled and ﬁxed within the linear region (12% local tissue strain) at multiple strain rates. Although samples were pulled to the same percent elongation, the ﬁbrils were noticed to elongate differently, increasing with strain rate. For the 0.1, 10, and 70%/s strain rates, there were 1.84+-3.6%, 5.5+-1.9%, and 7.03+-2.2% elongations (mean+-S.D.), respectively. We concluded that the collagen ﬁbrils underwent signiﬁcantly greater recruitment (ﬁbril strain relative to global tissue strain) at higher strain rates. A better understanding of tendon mechanisms at lower hierarchical levels would help establish a basis for future development of constitutive models and assist in tissue replacement design.
Three mature Japanese white rabbits were used for this study. Three tendons, all from different animals, were used in the study for interrupted mechanical testing and SEM analysis. The remaining patellar tendon samples were used for mechanical testing only. Both the proximal and distal insertion portions of the patellar tendon and the fascia surrounding the tendon were removed.The middle portion of the tendon was carefully extracted and then trimmed into four fascicles with the patella end attached to a holder and the other end grasped tightly with forceps (cut with an approximate width of 1mm (Yamamoto, 1999)). All fascicles used in the study were cut from the inner portions (the central 4mm)of the tendon to prevent location variability within the tendon (Williams et al.,2008). One tendon from each animal yielded 4 fascicles (extracted from the inner portion of tendon),among which 3 fascicles were used for tensile testing and 1 was used as a control sample.
Tendon fascicles were mounted onto the Biomomentum Mach-1 mechanical testing system (Biomomentum Inc.,Canada). Special grips were designed to secure the specimen and minimize slippage. All tested fascicles had grips initially at 7mm apart giving a ratio of the samples’ dimensions to be around 7:1(length vs.width), with each sample slightly varying in diameter. The fascicles were preconditioned in order to provide the specimens with similar loading histories and reduce variations in response to loading. Each sample was preloaded at 0.01 N at 0.01 mm/s; and zero strain (gauge length) was defined at this load. Each specimen was then preconditioned to a strain of 2%, for 10 cycles at 1 Hz (Yamamoto, 1999). The mechanical data were recorded in engineering stress and engineering strain. Control samples were subjected to the same preconditioning protocol and then fixed at a zero load in the fixative bath for the same amount of time (4 h). For the 4 fascicles yielded from each tendon, one was used as load free control and three were loaded to 20% clamp-to-clamp strain at 0.1, 10, and 70%/s strain rates. This corresponded to a 12% local strain in the midsubstance. Immediately after the test, the tendon was fixed in 1.25% glutaraldehyde for 4 h. The tangent modulus was taken from the linear portion of the curve at approximately 5% strain. Because of the inhomogeneous nature of tissue strain field from clamp-to-clamp, we monitored the local strain of midsubstance by placing two markers using permanent ink vertically on the fascicle surface and imaging the marker movement before and after the elongation. The local strain was calculated by measuring the distances between the centroids of two markers.
Samples for SEM were fixed in 1.25% glutaraldehyde in 0.1 M phosphate buffer (pH 7.2), rinsed with 0.1 M phosphate buffer, and post-fixed with 2% osmium tetraoxide in 0.1 M phosphate buffer. Samples were dehydrated in a graded ethanol series and then were critical point dried in a Polaron E 3000 CPD. They were then mounted on aluminum stubs and sputter coated with gold–palladium. Specimens were imaged using a JEOL JSM-6500 FE scanning electron microscope.After imaging,the samples were analyzed using Image J software (Image J 1.41,National Institutes of Health, USA).
The stress–strain curves showed strain rate sensitivity of tendon fascicles (Fig. 2). Strain rate sensitivity was verified by an increase in tangent modulus with a strain rate increase. The tangent moduli in the linear region were found to have values of 102+-42, 195+-58, and 251+-116 MPa for 0.1, 10, and 70%/s, respectively (Fig. 3). Tangent modulus values were found to be significantly different using post-hoc pair-wise comparisons vs. the quasistatic rate (p=0.05). There was no difference found between 10 and 70%/s strain rates(p=0.32) although there was an increase in trend.
The fixed fascicles were found to maintain their elongation after the removal of the tendon from the grips. SEM images showed a straightening of fibrils in strained fascicles compared with the less orderly control samples(Fig. 4). Elongation of the D-period was found to increase with strain rate increase(Fig. 5). For the control, 0.1, 10, and 70%/s fascicles, the average D-period lengths were found to be 51.3+-1.4, 52.2+-1.9, 54.1+-1.0, and 54.9+-1.2 nm, respectively. Statistical analysis found that all strain rates to be statistically significant from the control (p<0.005). Each rate was also compared with each other and also was found to be significant(p<0.001).
As expected,the analysis of the local midsubstance strain revealed anon-homogeneous strain field from clamp-to-clamp. However, our analysis showed that midsubstance strains for all 3 tests were around 12% in each strain rate group(10–14% local strain). Differences in local midsubstance strains were found to be insignificant among different strain rate groups. Mechanical data revealed fascicles were not pulled past the linear region.