Abstract
In legged locomotion, muscles undergo damped oscillations in response to the leg contacting the ground (an impact). How muscle oscillates varies depending on the impact situation. We used a custom-made frame in which we clamped an isolated rat muscle (M. gastrocnemius medialis and lateralis: GAS) and dropped it from three different heights and onto two different ground materials. In fully activated GAS, the dominant eigenfrequencies were 163 Hz, 265 Hz, and 399 Hz, which were signficantly higher (p < 0.05) compared to the dominant eigenfrequencies in passive GAS: 139 Hz, 215 Hz, and 286 Hz. In general, neither changing the falling height nor ground material led to any significant eigenfrequency changes in active nor passive GAS, respectively. To trace the eigenfrequency values back to GAS stiffness values, we developed a 3DoF model. The model-predicted GAS muscle eigenfrequencies matched well with the experimental values and deviated by − 3.8%, 9.0%, and 4.3% from the passive GAS eigenfrequencies and by − 1.8%, 13.3%, and − 1.5% from the active GAS eigenfrequencies. Differences between the frequencies found for active and passive muscle impact situations are dominantly due to the attachment of myosin heads to actin.
Similar content being viewed by others
Introduction
Muscles are soft tissues visco-elastically connected to the comparatively rigid skeletal system. Muscles can be displaced relative to the bone in response to a leg’s ground impact during terrestrial locomotion due to the soft coupling and distributed inertia within the musculoskeletal systems1,2,3. Such relative displacements of muscle masses are named “wobbling mass”1,2,4 dynamics. They are crucial factors in high-impact responses4, such as jumping or running, in which they critically shape the courses of the ground reaction force (GRF)5,6 as well as the joint moments and forces2,3,4,7, and significantly contribute to energy dissipation8,9,10,11.
The most common way to study wobbling mass dynamics in humans is either by using high-speed cameras to capture skin marker displacement following touch-down (TD)2,7,9 or by measuring the change in the electrical muscle activation in response to various types of impact strengths12,13 or ground properties1,12,14,15. Accordingly, Nigg and Wakeling (2001)13 introduced the concept of “muscle tuning”, arguing that muscles can tune (by changing activation patterns and thus the activity courses during impact responses) muscle fibre stress and thus stiffness and damping to avoid possible resonance. Resonance may occur if the frequencies of the input signal (deceleration of the bone) and the muscle responding by its wobbling-mass properties, i.e. its eigenfrequencies, are similar13,16.
How the muscle is tuned in impact situations depends, amongst other things, on muscle activation level13 and the interaction of mechanical lower limb and ground properties15. However, a disadvantage of examining human subjects to determine muscle frequencies in vivo is the potential mechanical effect of neighbouring bones or soft-tissue structures, such as fat and adjacent muscles, on the target muscle. In some cases, the momentum of attached devices, like accelerometers, let alone the potential systematic measurement errors due to skin attachment, which likely amplifies due to any device’s inertia and the skin movement artefacts (in determining bone positions), with the latter potentially also occurring even for markings painted on the skin2. In addition, there are regionally varying contributions to the overall whole-muscle oscillation17 because of the complex interaction between properties of tendons18,19, aponeurosis20,21, and muscle fibre material17.
So far, little is known of how the oscillation frequencies of muscles depend on the impact strength, as it is hard to address this issue with in vivo human experiments. Other than some activity dependence1,14, it has been suggested that the oscillation frequencies of muscles after an impact, or at least the dominant frequency, are independent of impact strength22. This is plausible because the stiffness of the fibre material likely stays the same if there is no change in muscle activity, i.e. the number of formed cross-bridges (CB) remains the same. However, an increase in impact strength leads to an increased oscillation amplitude22. Thus, depending on the impact strength, the CBs’ displacement paths on their force-length and force-velocity curve change, thereby potentially even changing these characteristics in themselves, which would shift the muscle’s oscillation frequencies.
Previously17, we have developed an experimental setup to analyse the wobbling mass dynamics of an isolated rat GAS muscle. For emulating a leg impact in rat locomotion, we dropped specimens of isolated GAS, clamped into a C-shaped frame11,17, onto a polystyrene cushion. Furthermore, we estimated the main eigenfrequency of a fresh and fully active GAS to be about 210 Hz. A huge advantage of our ex vivo setup is the direct control of the GAS’ initial impact conditions, i.e. its (isometric) force, the spatial position, the impact strength (e.g. by dropping height), and the deceleration time (e.g. by the frames ground contact material properties). Thus, GAS oscillatory responses can be manipulated by independently varying these conditions and properties. By making full use of our ex-vivo setup, this paper aims to determine the eigenfrequencies of fully activated and passive (GAS) muscle for different impact strengths (dropping heights) and ground material properties (polystyrene and aluminium). Secondly, we aim to trace several eigenfrequency values back to stiffness values of the main constituents, the fibre material, the tendons, and the aponeuroses’ regions.
Methods
Ethics
We performed all experiments on muscles (M. gastrocnemius medialis and lateralis: GAS) of freshly killed rats (Rattus norvegicus, Wistar). All experiments were carried out in accordance with ARRIVE guidelines and recommendations of the German animal welfare law (Tierschutzgesetz, §4 (3)). The protocol of this study was approved by the competent authority for animal welfare in Baden-Württemberg, Germany (Regierungspräsidium Stuttgart, Permit Number: 35-9185.81/0491). We anaesthetised the rats with sodium pentobarbital (100 mg per 1 kg body mass).
Experimental setup
Each GAS was dissected from its surrounding tissues, fixated (clamped) in a custom-made aluminium frame, and dropped from a pre-determined height on either polystyrene or aluminium (Fig. 1a). To measure muscle wobbling mass dynamics, the frontal surface of the muscle belly was patterned stochastically with high-grade steel markers (spheres, nominal diameter 0.4 mm, mensuration N0, IHSD-Klarmann, 96047 Bamberg, Germany) (Fig. 1b). These steel markers were held in place by the adhesive surface of the muscle belly in the same manner as the blunt bent wire that extended from the lower clamp (same procedure as in11,17). Before and after touch-down (TD) of the frame, we captured local muscle kinematics with two high-speed cameras (HCC-1000 BGE, VDS Vosskühler, 07646, Germany), each of which recorded with 256 × 1024 pixels per sample at 1825 Hz sampling rate. The frame consisted of a backbone with two extrusions to form an almost square C-shape, all made in aluminium.
The aluminium frame had mounted beneath the tip of the upper extrusion, in that order (all screwed to each other), a force transducer, an insulator, and the upper clamp for muscle fixation (Fig. 1a). Above the lower extrusion tip, an insulator was mounted to it, followed by the lower clamp for muscle fixation. Thus, the muscle was electrically insulated from the rest of the setup. We applied direct muscle stimulation (Aurora Scientific 701C) by 500 µs long square wave pulses of 12 V (three times the twitch threshold) generated at 100 Hz to ensure tetanic contraction23. We defined the optimal fibre length (\(L_{opt}\)) as the GAS length measured with the knee and ankle joints at 90° (\(L_{GAS,90^{\circ }}\)), plus an added 2 mm (\(L_{GAS,90^{\circ }}\,+\,2\,mm{\,=\,}L_{opt}\)), with the latter value inferred from literature23,24. This experimental setup is described in more detail elsewhere11.
Experimental trials
In this study, we used our GAS specimens (N = 25) to conduct the following trials: dropping GAS onto polystyrene from either 1 cm, 1.5 cm, or 4 cm height, as well as dropping GAS onto aluminium from 2 mm. We labelled these trials group 1 (1 cm trials), group 2 (1.5 cm trials), group 3 (4 cm trials), and group 4 (aluminium trials), respectively, which contained both active (A\(_i\)) and passive (P\(_i\)) trials within each group 1–4 (Table 1). All trials within each group started with fully stimulated GAS trials, ensuring maximal (initially non-fatigued) isometric force (\(F_{max}\)) at TD, followed by trials without muscle stimulation, i.e. passive GAS trials.
Spectral analysis
We used our captured time-velocity data of GAS to determine frequency spectra. We analysed the data between TD and the instant at which the acceleration of the arithmetic mean of all belly markers (\(a_{COM}\)) returned to zero for the second time (after \(\approx\) 17 ms). The position of the GAS’ centre of mass (COM) was estimated with the kinematic information from all markers (arithmetic mean) as in previous studies11,17.
To transform our time domain signal into the frequency domain
We used the Cooley–Tukey algorithm25,26 [Eq. (1)], with N being the number of samples, n the time index, k the frequency index, y(n) the input signal amplitude at sample n, and i the imaginary unit defined by \(i =: \sqrt{-1}\). Due to the short length of the analysed period, the frequency resolution of our captured time-velocity data would have actually been only about 59 Hz (1\(\div\)0.017 s). However, the captured time domain data were extended by padding trailing zeros to create 256-point data sets, which methodically provided a frequency resolution of about 7.1 Hz (1825 Hz\(\div\)256). In each trial, we normalised the frequency amplitudes of the calculated spectrum to their maximum value (\(Y_{0}\)).
GAS 3DoF model: spring stiffness
To look for frequencies due to GAS oscillations in the spectral analysis, we treated the GAS as an undamped system with three point masses in series connected by linear springs (3DoF model, Fig. 1c), with the sum of the point masses being the GAS’ mass (\(m_{GAS}\)). This model system is fixated at both ends (clamped between origin and insertion) and can oscillate in only one dimension, namely the GAS’ longitudinal axis (Fig. 1c). To explain our model and the reasoning behind our assumptions, we have separated the GAS 3DoF model method section into three sections: “spring stiffness”, “mass”, and “eigenfrequencies and local muscle stiffnesses”.
With our simple model approach, we assume that the muscle belly and aponeuroses are similar in shape and elastic properties proximally and distally. Moreover, we separate the GAS region that solely contains fibre tissue from the rest of the GAS tissues. Accordingly, we do not consider inhomogeneities27,28 and anisotropies21 of the aponeuroses at this stage, nor the complex interaction of aponeuroses and fibre material in their overlapping zones. Such a 3DoF model would allow for differences in proximal and distal tendon stiffnesses (\(k_{t,p}\) and \(k_{t,d}\), respectively) due to differences in proximal and distal tendon lengths (Table 1). However, because Young’s modulus of leg tendon material is \(\approx\)1.5 GPa18,19, which makes any estimated \(k_{t,p}\) or \(k_{t,d}\) minimally 10 and up to 50 times higher, respectively, than each (proximal or distal) combined aponeurosis and part of fibre stiffness in fully active GAS (the stiffness of the combination of the two tendon-aponeurosis-fibre complexes termed \(k_{TAC}\)17), we simplify the elastic properties of the most proximal and distal (the ‘outer’) springs (Fig. 1c) to each the same stiffness
As a consequence, the other two (‘inner’) springs connecting the mass in the centre of the muscle model to the other two masses are likewise identical (their stiffness: \(k_{SC}\), see Fig. 1c). Both ‘inner’ springs are composed of the stiffness of fibre material solely (\(k_{C}\)) in series with \(k_{S}\):
In both directions, the stiffness of the fibre material \(k_C\) is arranged adjacently to \(m_C\) (Fig. 1c). As we assume proximal-distal stiffness symmetry, we further say that
and
as the springs on either side of a point mass (\(m_{S,p}\), \(m_{C}\), or \(m_{S,d}\)) act in parallel (see the cubic equation, Supplementary Text S1), which is also indirectly seen in Eq. (10), where the eigenvector of \(m_C\) is zero (eigenvector for \(freq _{2}\), Supplementary Eq. S20, p. 5).
GAS 3DoF model: mass
As seen in Fig. 1c, the lumped mass located in the centre of our model (\(m_{C}\)) is attached to only \(k_{C}\); hence, that mass signifies fibre material only. We estimate the mass
located in this central, fibre-only region of GAS, with 0.75 cm and 0.86 cm2 being its length and average ACSA (\(ACSA_{avr}\))11, respectively, and 1.06 g/cm3 the fibre material density29. Therefore, we can reasonably assume both stiffness and mass symmetry, namely
because \(m_{GAS}\) = 1.9 g (Table 1; mean group1 value of 1.9 g are the same in our present and earlier11 study). From Eq. (6), it is also clear that fibre material mass dominates \(m_{S,p|d}\) because overall tendon mass, grossly, only makes up 4% (\(\frac{0.03\,\text {g}}{0.63\,\text {g}}\)):
In Eq. (8), 1.12 g/cm3 is the density of tendon30, 0.024 cm2 the Achilles tendon ACSA (mean value from11,17), and 1.2 cm the total tendon length (Table 1).
GAS 3DoF model: eigenfrequencies and stiffnesses comparisons to literature
In this study, the experimental setup and the captured time displacement data is the same as in Christensen et al.11, which also included the same passive and \(F_{max}\) trials as the 1 cm trials here (group 1). For this reason, we only applied our 3DoF model (Fig. 1c) on passive (P1) and active (A1) group1 trials.
We grossly assume that the muscle has at least three separable regions: each a proximal and distal tendon-aponeurosis-fibre region, which are mechanically identical [Eqs. (7) and (2)], plus a fibre-only region in the muscle centre. Hence, in the core of our model, we have only two stiffness parameters, which are \(k_S\) and \(k_C\), respectively, and three masses m of identical value [Eq. (7)]. Because of this simplistic approach, the model is separable into units of either \(k_{SSC}\) [Eq. (4)] or \(k_{SC2}\) [Eq. (5)]; as such, the eigenfrequencies of the model are
For more information regarding the deduction of Eqs. (9) and (10), and if \(m_{S,p}=m_{S,d}\ne m_C\), see Supplementary Text S1.
In our previous study11, the whole GAS’ muscle-tendon-complex was modelled by just one overall muscle mass (measured) suspended on the frame by one overall spring with a stiffness \(k_{MTC}\) (measured), and the latter was further assumed to consist of a serial arrangement of an inferred overall tendon-aponeurosis-complex stiffness \(k_{TAC}\) and a measured fibre material stiffness \(k_{CE}\) of the fibre-only (contractile element, CE) muscle centre:
With both \(k_{MTC}\) and \(k_{CE}\) [Eq. (11)] calculated using the (measured) dynamic force change in response to TD (\(\Delta F=m_{GAS}\cdot a_{COM}\)) and either the displacement of the COM (\(\Delta L_{MTC}\)) or the fibre material elongation, respectively, both likewise measured in response to TD, \(k_{TAC}\) was
there.
Here, however, the model is instead treated as a 3DoF symmetrical spring-mass system with at both ends fixated, i.e. a clamped (and pre-strained) system, where the distal-proximal symmetry in both stiffness [Eqs. (2) and (3)] and mass [Eq. (7)], makes the displacement of \(x_C\) (Equations of motion, Supplementary Eq. S4, p. 2)
assuming that the displacement \(m_{S,p}\) is half of \(m_C\). When further assuming that \(\Delta L_{MTC}=x_C\) is the same as in Eq. (12), being a measured quantity for the centre of mass displacement after TD, then
which makes the ratio between \(k_{TAC}\) [Eq. (12)] inferred from experiments11 and our model parameter \(k_S\) [Eq. (16)] correspond to
where we find \(c_a=3.7\) and \(c_p=2.7\) for active and passive GAS, respectively (Supplementary Text S3). Likewise, the model parameter to determine fibre material stiffness is
because the length of the CE region (which spans the GAS’ COM) at the instant before TD (\(L_{CE,0}\)) is a quantity used to estimate Young’s modulus of the fibre material \(E_{CE}\) = 1.3 MPa11. To keep Young’s modulus the same, the stiffness of the fibre material must be \({k_{C}}=k_{CE}\cdot 2\) at \(\frac{L_{CE}}{2}\), which is the length of one \(k_C\) spring:
Statistical analysis
All the statistical tests were calculated using a one-way ANOVA with the Bonferroni adjustment for multiple comparisons, with the values presented as mean ± SD. Differences were statistically significant when p \(\,\le \,\alpha\) = 0.05 or p \(\,\le \,\alpha ^*\) = \(\alpha\)/n for the Bonferroni correction, with n being the number of performed tests.
Results
In our spectral analysis, we determined eight frequencies, which we labelled \(F1-F8\).
When comparing these measured frequencies in more detail in active and passive GAS, we found no significant differences between the frequencies labelled F1, F5, and F8, whereas F2 and F3 significantly differed and can thus be attributed to GAS (compare Tables 2 and 3). Frequencies F1, F5, and F8 can be attributed to eigenfrequencies of the frame (compare Tables 2 and 4) interacting with the ground material or oscillating in itself. F7 significantly differ when comparing passive and active GAS (p = 0.02, Table 5) but is close to similar eigenfrequencies of the frame interacting with the ground material. The other four frequencies (F2, F3, and \(F4\) \(\vert\) \(F6\), Table 5) measured in the passive and active GAS conditions can hence be concluded to reflect GAS eigenfrequencies. Further, F4 (see both top and bottom in Table 2, and compare with Table 3, top, \(freq _{3}\)) was not present in the active trials, whereas, in the passive trials, F6 (see both top and bottom in Table 2, and compare with Table 3, bottom, \(freq _{3}\)) was not present (Table 2, top and Fig. 2). The difference in active and passive GAS frequencies is, as an exemplary case, visualised in Fig. 3.
The replacement of polystyrene by aluminium as the ground material generally removed F1 at about 60 Hz from the measured spectra (P4 and A4, Table 2). Still, the remaining frequencies neither changed significantly with ground material in the active nor in the passive trials, except F2, slightly, within the passive trials (135 Hz and 141 Hz, p = 0.043, see Table 2).
Increasing the impact strength by dropping height (1 cm, 1.5 cm and 4 cm trials) did not cause significant changes in passive GAS frequencies. This likewise applies to the active trials (Fig. 4), with the only exception being the (slight) difference between A2 (466 Hz) and A3 (489 Hz, p = 0.035 in Table 2). Despite the frame eigenfrequencies F5 and F8 being present in some of the passive 1.5 cm trials, and F7 in the 4 cm trials, these were excluded from Table 2, because they were not present in every trial. Likewise, F5 in A1 and A2 are not included in Table 2. For statistical comparisons of active and passive trials, see Supplementary Table S1.
As seen in Eqs. (9) and (10), only the two composite stiffnesses \(k_{SSC}\) and \(k_{SC2}\) are used to determine the eigenfrequencies of the model. If the stiffness values of active GAS (Table 3, centre, bottom) are used as an input to the model, then the 3DoF model-predicted eigenfrequencies are 162 Hz, 298 Hz, and 386 Hz (Table 3, bottom, right). The deviations of these theoretical eigenfrequencies relative to the average values of the measured active GAS frequencies (F2, F3, and F6 in Table 2, A1) are − 1.8% (\(\frac{(162-165)\,\text {Hz}}{165\,\text {Hz}}\)), 13.3% (\(\frac{(298-263)\,\text {Hz}}{263\,\text {Hz}}\)), and − 1.5% (\(\frac{(386-392)\,\text {Hz}}{392\,\text {Hz}}\)), respectively. In the passive GAS, the 3DoF model-predicted eigenfrequencies are 126 Hz, 229 Hz, and 293 Hz (Table 3, top, right). These deviate by -3.8% (\(\frac{(126-131)\,\text {Hz}}{131\,\text {Hz}}\)), 9.0% (\(\frac{(229-210)\,\text {Hz}}{210\,\text {Hz}}\)), and 4.3% (\(\frac{(293-281)\,\text {Hz}}{281\,\text {Hz}}\)), respectively, from their measured counterparts (F2, F3, and F4 in Table 2, P1).
Discussion
When comparing the frequencies in Tables 2 and 4, it is likely that the frequencies at about 60 Hz, 330 Hz, 355 Hz, 450 Hz and 550 Hz reflect properties of the interaction between the frame itself and the ground material because these frequencies are still present without the GAS fixated in the frame. Further, the frequency at \(\approx\) 60 Hz disappears in the FFT analysis when changing the ground material from polystyrene to aluminium. Thus, the \(\approx\) 60 Hz in the FFT analysis is attributed to the polystyrene-frame interaction.
Across all trials, the frequencies attributed to GAS are always lower in passive trials (Table 5). As all three GAS frequencies (F2, F3, and \(F4\) \(\vert\) \(F6\)) depend on (active and passive) fibre material properties (Table 3: through the basic model stiffnesses \(k_{C}\) and \(k_{S}\), Fig. 1c, thus \(k_{SC}\) and \(k_{SSC}\), see Eqs. (3) and (4)], the positive correlation between frequency and muscle activity is likely due to forming cross-bridges. In active fibre material, attaching myosin heads mechanically couple actin and myosin filaments by building cross-bridges, and the filament sliding requires their distortion31,32. Furthermore, any added cross-bridge increases the fibre material stiffness31,33. In a study11 similar to our present one, we found that the stiffness in fully activated fibre material only (not \(k_{S}\) representing fibre-aponeurosis properties, but \(k_{C}\) here equalling \(k_{CE}\) there11) is \(\approx\) 370% (\(\frac{15,000\,\text {N m}^{-1}-3200\,\text {N m}^{-1}}{3200\,\text {N \, m}^{-1}}\)) higher than in the passive fibre material11 (see also Supplementary Table S4). Active muscle contraction also biaxially loads the aponeurosis27,34, and at least one study21 has shown in isotonic contraction experiments that the longitudinal stiffness of the probed aponeuroses of wild turkeys’ M. gastrocnemius lateralis increased by \(\approx\) 64% (\(\frac{180\,\text {N \, m}^{-1}-110\,\text {N \, m}^{-1}}{110\,\text {N \, m}^{-1}}\), [Fig. 5B21]) from the passive to the fully activated muscle condition. We assume that either the aponeuroses17,21 or fibre material11 dominate F2 due to their estimated stiffness values being at least an order of magnitude lower than that of the longer (proximal) GAS tendon, with tendon stiffness estimates being based on published values of Young’s modulus30,31. Unfortunately, with our present 3DoF model and current experimental setup, we can still not resolve the individual tissue contributions or potential differences in proximal and distal stiffness values.
One frequency (F7) that we found in the passive (455 Hz) condition did significantly differ from its active counterpart (470 Hz). Both of these frequencies are also slightly different from any frame or frame-ground-material frequencies (polystyrene, Table 4), nor does the 3DoF model predict them. Therefore, either the 3DoF model is too simple (e.g., too few degrees of freedom) to predict these frequencies or that the interaction between GAS and both frame extrusions slightly alters the overall stiffness of the muscle preparation. If the latter is the case, then this might also affect F2 in Table 4, whereas the lowest frame-ground-material frequency found remains the same because the frame mass and polystyrene visco-elasticity determine it.
For the active and passive trials, changing the impact strength leads to no significant changes in the frequency spectrum. Our findings might differ with a higher impact strength because for a fresh and fully stimulated GAS, the impact strength in the 4 cm trials is insufficient to induce forcible cross-bridge disruption17. Here, the impact strength is not enough to interfere significantly with the work-stroke: whether by forcible rupture of cross-bridge bonds35 or influence of the centre of oscillation at which the cross-bridge generates GAS’ maximum contractile force. Changing the impact strength may alter the oscillation amplitudes, however, issues like potential elastic recoil by wobbling masses, their dissipating energy, and wave propagation, all as functions of impact strength and thus their oscillation amplitudes, have not been a part of this study, although very worth while investigating next.
There were no significant differences in active GAS frequencies when comparing the aluminium (2 mm) trials and the 1.5 cm polystyrene trials (Supplementary Table S2). A likely explanation and an advantage of our setup is the controlled environment in which we can design impact situations on GAS that are complicated or impossible to specifically aim at in situ. For example, the lower limb muscles are not pre-activated in a tuned fashion1,12,13,14 in our experiments, and the lower limb is not pre-angled36,37, respectively, which allows us to reduce the expected complexity of the vibrational soft tissue response (here, e.g., focussing on longitudinal oscillation modes solely). In our results, we then find that in the pretty low-dimensional solution space of just a few frequencies only one of them, namely, F2 in the passive 1.5 cm trials (135 Hz) differs significantly from the likewise passive aluminium trials (141 Hz), with about the same impact strength (Table 2). We suspect that this (slight albeit significant: p = 0.043, Supplementary Table S1) difference in F2 may be accounted for by either the time between the last active trial and the passive one performed, or the time between dissection and the passive experiments, or the total number of experiments for a specific muscle. Such suspected memory or history mechanism may be structure-inherent: An appropriate hypothesis would be that this originates from the third filament, the giant molecule titin. Titin likely contributes \(\ge\) 75% of the passive stiffness in fibre material at \(L_{opt}\)11, and titin is a visco-elastic material38,39. Titin’s mechanical effects, e.g. through its interaction with actin40, are determined by the contractile (both mechanical and activity) history and, thus and accordingly, vary with the time between each stretch/shortening contraction38,41. Unfortunately, again, due to formal restrictions (so far, only a few animals are available in each experimental session), and the overall methodical complexity of the setup, our sample sizes are currently simply too small, and our data is too few, to explore any of these potential correlations, up to now.
In general, our model-predicted GAS muscle eigenfrequencies match well in both cases probed in experiments, the passive (P1) and the fully active (A1). We show that treating the muscle as a system clamped by an alternating sequence of pre-strained, linear springs and portions of muscle mass (i.e. a system of serially coupled harmonic oscillators) quite accurately estimates GAS eigenfrequencies in response to the impact at TD, when at least two criteria are met: First, the muscle must be, initially (at TD), in near-isometric conditions, which is in agreement with the literature, as the angle flexion in the knee and ankle joint within the first 20 ms after TD is just \(\approx\) 3° for Tupaia glis trotting at 1 m s−142; i.e. GAS is stiff at TD, and both joint angular velocities are close to zero. The second criterion probably allows for more scope in active muscle length before TD, as contracting fibre material can compensate for any initial slackness. We also show that the elasticities of both aponeuroses and the fibre material dominate the high amplitude GAS eigenfrequencies and that any elasticity of tendon material on GAS eigenfrequencies are likely non-existent because of the differences in stiffnesses and mass compared to other GAS tissues. As rat GAS (distal) tendon length is not extraordinarily short, this should likewise apply to any other vertebrate of rat size or smaller18,43 because Young’s modulus18,19 then completely determines stiffness. Due to pure mechanical (inertia and compliance) reasons, in bigger animals with lower eigenfrequencies17, tendons may well play a significant role in muscle wobbling mass eigenfrequencies where \(k_{t,d}\) and even \(k_{t,p}\), with \(k_{t,p} \ne k_{t,d}\), should be considered at first instance when analysing the eigenfrequencies of muscles bigger than rat GAS.
Whereas the first (\(freq _{1}\)) and third (\(freq _{3}\)) model-estimated eigenfrequencies (Table 3) are in almost perfect agreement with the two comparable experimentally found eigenfrequencies (F2 and \(F4\) \(\vert\) \(F6\), Table 2), the second estimated eigenfrequency (\(freq _{2}\)) does deviate more from measured F3 than its counterparts. As we assume proximal and distal symmetry in both stiffness and mass, the absolute displacements of \(m_{S,p}\) and \(m_{S,d}\) are always the same (see Fig. 1c and our 3DoF model’s eigenvectors in Supplementary Eqs. S20, S22, S23, p. 5, respectively). Therefore, our present model cannot cover any potential non-homogeneous fibre strain distribution (wave propagation) across the centre part (the belly made of fibres: CE, Fig. 1c) bar for the case of the eigenvector of \(freq _{2}\) where the displacement of \(m_{S,p}\) and \(m_{S,d}\) is in opposite directions (Supplementary Eq. S20, p. 5). Not allowing fibre strain in any in-phase eigenvector contradicts literature that found \(\approx\) 0.3% fibre strain at \(F_{max}\) in wobbling mass experiments similar to our group3 trials17. To meet some fibre strain, either proximal-distal mass asymmetry or asymmetry in proximal and distal stiffnesses must be considered in the model. Any breaking of the proximal-distal model symmetry may include the necessity to improve our model explanations to the measured eigenfrequencies and -modes; yet, this demands to enhance the model complexity by adding degrees of freedom. Increasing the model complexity by adding degrees of freedom would, in turn, allow for better distinguishing anatomically defined tissue regions within GAS (i.e. exactly distinguishing and representing tendons, as well as mixed aponeurosis-fibre and pure fibre regions, respectively) and more transparently examining, and thus understanding, their contribution to the wobbling mass dynamics.
Conclusion
Based on our findings, we conclude that the differences between the harmonic frequencies of impact-induced strain oscillations of passively clamped and actively contracting isometric rat GAS muscles are dominantly due to the attachment of myosin heads to actin (cross-bridges). That means the more cross-bridges, the higher the stiffness and the higher the GAS eigenfrequencies. Changing the GAS stiffness affects all frequencies that are certainly attributable to the muscle only in our experiments. We found that neither changing the impact strength, nor the ground material, influenced active or passive GAS frequencies significantly. With only three degrees of freedom, our model can explain at least two of the GAS frequencies measured in both the passive and the active conditions. It will be exciting to see whether very moderate enhancements of our present model (e.g. adding just one additional degree of freedom) are attending enhanced explanatory power regarding the wobbling mass dynamics.
Data availability
The datasets used and/or analysed during the current study available from the corresponding author on reasonable request.
References
Wakeling, J. M. & Nigg, B. M. Soft-tissue vibrations in the quadriceps measured with skin mounted transducers. J. Biomech. 34, 539–543 (2001).
Günther, M., Sholukha, V. A., Keßler, D., Wank, V. & Blickhan, R. Dealing with skin motion and wobbling masses in inverse dynamics. J. Mech. Med. Biol. 3, 309–335 (2003).
Pain, M. T. G. & Challis, J. H. The influence of soft tissue movement on ground reaction forces, joint torques and joint reaction forces in drop landings. J. Biomech. 39, 119–124 (2006).
Gruber, K., Ruder, H., Denoth, J. & Schneider, K. A comparative study of impact dynamics: Wobbling mass model versus rigid body models. J. Biomech. 31, 439–444 (1998).
Nigg, B. M. & Liu, W. The effect of muscle stiffness and damping on simulated impact force peaks during running. J. Biomech. 32, 849–856 (1999).
Gittoes, M. J. R., Brewin, M. A. & Kerwin, D. G. Soft tissue contributions to impact forces simulated using a four-segment wobbling mass model of forefoot-heel landings. Hum. Movem. Sci. 25, 775–787 (2006).
Bélaise, C., Blache, Y., Thouzé, A., Monnet, T. & Begon, M. Effect of wobbling mass modeling on joint dynamics during human movements with impacts. Multibody Syst. Dyn. 38, 345–366 (2016).
Zelik, K. E. & Kuo, A. D. Human walking isn’t all hard work: Evidence of soft tissue contributions to energy dissipation and return. J. Exp. Biol. 213, 4257–4264 (2010).
Schmitt, S. & Günther, M. Human leg impact: Energy dissipation of wobbling masses. Arch. Appl. Mech. 81, 887–897 (2011).
Riddick, R. C. & Kuo, A. D. Soft tissues store and return mechanical energy in human running. J. Biomech. 49, 436–441 (2016).
Christensen, K. B., Günther, M., Schmitt, S. & Siebert, T. Cross-bridge mechanics estimated from skeletal muscles’ work-loop responses to impacts in legged locomotion. Sci. Rep. 11, 23638 (2021).
Nigg, B. M., Bahlsen, H. A., Luethi, S. M. & Stokes, S. The influence of running velocity and midsole hardness on external impact forces in heel-toe running. J. Biomech. 20, 951–959 (1987).
Nigg, B. M. & Wakeling, J. M. Impact forces and muscle tuning: A new paradigm. Exerc. Sport Sci. Rev. 29, 37–41 (2001).
Wakeling, J. M. & Nigg, B. M. Modification of soft tissue vibrations in the leg by muscular activity. J. Appl. Physiol. 90, 412–420 (2001).
Fu, W. et al. Surface effects on in-shoe plantar pressure and tibial impact during running. J. Sport Health Sci. 4, 384–390 (2015).
Boyer, K. A. & Nigg, B. M. Soft tissue vibrations within one soft tissue compartment. J. Biomech. 39, 645–651 (2006).
Christensen, K. B., Günther, M., Schmitt, S. & Siebert, T. Strain in shock-loaded skeletal muscle and the time scale of muscular wobbling mass dynamics. Sci. Rep. 7, 13266 (2017).
Alexander, R. M. Tendon elasticity and muscle function. Comp. Biochem. Physiol. A 133, 1001–1011 (2002).
Ker, R. F. Mechanics of tendon, from an engineering perspective. Int. J. Fatigue 29, 1001–1009 (2007).
Zuurbier, C. J., Everard, A. J., van der Wees, P. & Huijing, P. A. Length-force characteristics of the aponeurosis in the passive and active muscle condition and in the isolated condition. J. Biomech. 27, 445–453 (1994).
Azizi, E. & Roberts, T. J. Biaxial strain and variable stiffness in aponeuroses. J. Physiol. 587, 4309–4318 (2009).
Deng, L. et al. Compression garments reduce soft tissue vibrations and muscle activations during drop jumps: An accelerometry evaluation. Sensors 21, 5644 (2021).
Siebert, T., Till, O. & Blickhan, R. Work partitioning of transversally loaded muscle: Experimentation and simulation. Comput. Methods Biomech. Biomed. Eng. 17, 217–229 (2014).
De Koning, J. J., van der Molen, H. F., Woittiez, R. D. & Huijing, P. A. Functional characteristics of rat gastrocnemius and tibialis anterior muscles during growth. J. Morphol. 194, 75–84 (1987).
Cooley, J. W. & Tukey, J. W. An algorithm for the machine calculation of complex Fourier series. Math. Comput. 19, 297–301 (1965).
Mneney, S. An Introduction to Digital Signal Processing: A Focus on Implementation (River Publishers, 2009).
Böl, M. et al. Novel microstructural findings in M. plantaris and their impact during active and passive loading at the macro level. J. Mech. Behav. Biomed. Mater. 51, 25–39 (2015).
Finni, T., Hodgson, J. A., Lai, A. M., Edgerton, V. R. & Sinha, S. Nonuniform strain of human soleus aponeurosis-tendon complex during submaximal voluntary contractions in vivo. J. Appl. Physiol. 95, 829–837 (2003).
Urbanchek, M. G., Picken, E. B., Kalliainen, L. K. & Kuzon, W. M. Jr. Specific force deficit in skeletal muscles of old rats is partially explained by the existence of denervated muscle fibers. J. Gerontol. Ser. A 56, B191–B197 (2001).
Ker, R. F. Dynamic tensile properties of the plantaris tendon of sheep (Ovis aries). J. Exp. Biol. 93, 283–302 (1981).
Piazzesi, G. et al. Skeletal muscle performance determined by modulation of number of myosin motors rather than motor force or stroke size. Cell 131, 784–795 (2007).
Huxley, A. F. Muscle structure and theories of contraction. Prog. Biophys. Biophys. Chem. 7, 255–318 (1957).
Colombini, B., Bagni, M. A. & Griffiths, P. J. Effects of solution tonicity on crossbridge properties and myosin lever arm disposition in intact frog muscle fibres. J. Physiol. 578, 337–346 (2007).
Raiteri, B. J. Aponeurosis behaviour during muscular contraction: A narrative review. Eur. J. Sport Sci. 18, 1128–1138 (2018).
Weidner, S., Tomalka, A., Rode, C. & Siebert, T. How velocity impacts eccentric force generation of fully activated skinned skeletal muscle fibers in long stretches. J. Appl. Physiol. 133, 223–233 (2022).
Dixon, S. J., Collop, A. C. & Batt, M. E. Surface effects on ground reaction forces and lower extremity kinematics in running. Med. Sci. Sports Exerc. 32, 1919–1926 (2000).
Voloshina, A. S. & Ferris, D. P. Biomechanics and energetics of running on uneven terrain. J. Exp. Biol. 218, 711–719 (2015).
Mártonfalvi, Z. et al. Low-force transitions in single titin molecules reflect a memory of contractile history. J. Cell Sci. 127, 858–870 (2014) (Figure S4c).
Rivas-Pardo, J. A. et al. Work done by titin protein folding assists muscle contraction. Cell Rep. 14, 1339–1347 (2016).
Rode, C., Siebert, T. & Blickhan, R. Titin-induced force enhancement and force depression: A ‘sticky-spring’ mechanism in muscle contractions?. J. Theor. Biol. 259, 350–360 (2009).
Tomalka, A., Weidner, S., Hahn, D., Seiberl, W. & Siebert, T. Power amplification increases with contraction velocity during stretch-shortening cycles of skinned muscle fibers. Front. Physiol. 12, 391 (2021).
Schilling, N. & Fischer, M. S. Kinematic analysis of treadmill locomotion of tree shrews, Tupaia glis (Scandentia: Tupaiidae). Z. Säugetierk. 64, 129–153 (1999).
Günther, M. et al. Rules of nature’s formula run: Muscle mechanics during late stance is the key to explaining maximum running speed. J. Theor. Biol. 523, 110714 (2021).
Acknowledgements
This work was funded by the ‘Deutsche Forschungsgemeinschaft’ (DFG) grants SI841/7-3 and SCHM2392/5-3 (Project Number: 234087184) to T.S. and S.S., respectively.
Funding
Open Access funding enabled and organized by Projekt DEAL.
Author information
Authors and Affiliations
Contributions
K.C., M.G., S.S. and T.S. developed the ideas and drafted the manuscript. K.C. and M.G. wrote the initial text of the manuscript. S.S. and T.S. repeatedly revised the manuscript. K.C. constructed and built the impact apparatus and performed the experiments. K.C. and M.G. analysed the data. All authors gave final approval for publication.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Christensen, K.B., Günther, M., Schmitt, S. et al. Muscle wobbling mass dynamics: eigenfrequency dependencies on activity, impact strength, and ground material. Sci Rep 13, 19575 (2023). https://doi.org/10.1038/s41598-023-45821-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-023-45821-w
- Springer Nature Limited
We’re sorry, something doesn't seem to be working properly.
Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.