Viscoelastic properties of skeletal muscle are associated with a complex network of cytoskeletal proteins where titin and nebulin play a substantial role. The need for evaluation of muscle viscoelastic properties is widely accepted in clinical use to evaluate the effect of treatment or progression of muscle pathology (atrophy). We tested the hypothesis that the viscoelastic properties (elasticity, tone and stiffness) change in atrophied muscles with concomitant changes in cytoskeletal proteins (titin, nebulin) and contractile protein (myosin heavy chain) proportion. Sixteen 24- week-old male rats of the Wistar strain were randomly allocated to two groups: dexamethasone group treated each day for 10 consecutive days with dexamethasone in order to induce atrophy and control group. Skeletal muscle viscoelastic properties (elasticity, tone and stiffness) were determined using a myotonometer. Titin, nebulin and myosin heavy chain content were quantified using SDS-PAGE electrophoresis. We found that glucocorticoid-induced muscle atrophy is accompanied by reduced elasticity and increased tone and stiffness, with concomitant changes in titin, nebulin and myosin heavy chain con- tent. The elasticity decreased by 10.9% (P < 0.05), tone increased from 26.69 Hz to 37.73 Hz (P < 0.05), and stiffness was significantly lower in dexamethasone group (627.3 N/m vs 758.6 N/m); (P < 0.05). Compared with the control group, the content of titin, nebulin and myosin heavy chain in atrophied muscle was 76.4%, 70.6% and 82.3%, respectively. Our results may lead to a better understanding of the mechanism of muscle atrophy and provide better guidance for rehabilitation practices and help to find rational therapeutic intervention in the future.
The function and properties of skeletal muscle are complex and consist of integrated functions of several structures. The need for evaluation of muscle viscoelastic properties is widely accepted in clinical use to evaluate the effect of treatment or progression of pathology (atrophy).
Elastic properties of skeletal muscle are associated with a complex network of cytoskeletal proteins where titin and nebulin play a substantial role. Nebulin is a part of thin filament. Titin forms a third myofilament system connecting the A-band to the I-bands and Z-line and possess particularly elastic properties. In addition to their structural role, titin and nebulin are involved in the production of active and passive tension in the muscle [1-3].
Glucocorticoids (GCs) are the most potent immunosuppressive and anti-inflammatory drugs widely used for the treatment of patients with a variety of disorders. The application of glucocorticoids has been limited due to the side effects, especially upon long-term and high doses. The catabolic effects of GCs on skeletal muscle are mediated via several cellular mechanisms. GCs inhibit muscle protein synthesis, stimulate protein degradation in skeletal muscle and are an important factor in the development of muscle atrophy. Muscle atrophy is characterised by a reduction in several muscle proteins, contributing to impaired muscle function. Dexamethasone is a synthetic compound that has anti-inflammatory effects similar to those of natural GCs.
The model of dexamethasone-induced atrophy has been used in several previous studies in our laboratory [4-7]. For example, the administration of glucocorticoids decreased the turnover rate of myosin heavy chain (MHC) and reduced the proportion of fast type MHC isoforms [
The changes in cytoskeletal proteins such as titin and nebulin have repeatedly been examined using different models of muscle atrophy: the relative amount of titin and/or nebulin decreases after hind-limb unloading [8,9], after denervation [
To our knowledge, only Hayashi et al. [
Therefore, we tested the hypothesis whether the viscoelastic properties of atrophied muscle change with concomitant changes in titin and nebulin.
The animals used in the study were male rats of the Wistar strain (Scanbur BK AS Sollentuna, Sweden) that were 24 weeks old at the beginning of the experiment.
The rats were assigned to control (Contr) (n = 8) and dexamethasone (Dex) (n = 8) groups. Dexamethasone (Dexafort 3 mg/ml; International B.V. Boxmeer, The Netherlands) was diluted to 200 µg/ml with 0.15 M NaCl and administered intraperitoneally at 100 µg/100 g body weight (bw) daily for 10 days. The control animals received appropriate amounts of 0.15 M NaCl. The animals were anaesthetised by intraperitoneal injection of ketamine (2.5 mg/100 g bw) (Calysol, Gedeon Richter A.O. Budapest, Hungary) and diazepam (2.5 mg/100 g bw) (Lab Renaudin, France). The experimental protocol was approved by the Animal Experimentation Committee at the Estonian Ministry of Agriculture.
The central part of the muscle belly of the gastrocnemius muscle (Gas) of the anaesthetised rats was tested five times with a pause of 1 s. The testing end of the device was placed on the surface of the skin above the peripheral muscle under investigation. The electromagnet contained in the device produces a short constant force impulse, which is transmitted via the testing end to the contact area. The impulse terminates in a quick release, and this mechanical influence induces damped natural oscillation in the muscle under investigation [
Hind-limb grip strength was measured before and after 10 days of dexamethasone treatment using a Grip Strength Meter 0167-004L (Columbus Instruments, USA).
The extensor digitorum longus (EDL) and Gas muscles were dissected, trimmed of visible fat and connective tissue, weighed, frozen in liquid nitrogen, and stored at −80˚C until further processing.
The titin, nebulin and MHC content of muscle samples was determined by gradient 2.8% - 12% SDS-PAGE according to the previously described method [
The gel slab was stained with PageBlueTM Protein Staining Solution (Fermentas, Canada), and the protein bands were analysed densitometrically using the Image Master® 1D Program, Version 3.0 (Amersham Pharmacia Biotech, UK).
The optical density integrals (ODI) of total titin (T1 + T2), nebulin and total MHC, were measured for each loading volume, and the slope of the relationship between the ODI and loading volume was determined by linear regression analysis. The ratios of titin/MHC, nebulin/MHC, and nebulin/titin were calculated.
MHC isoforms proportion was determined by 8% SDSPAGE [
Muscle samples were prepared for MHC isoforms electrophoresis as described previously. Frozen muscles were thawed on ice, cut into small pieces, and washed with five volumes 20 mM NaCl, 5 mM sodium phosphate, 1 mM EGTA (pH 6.5). Myofibrillar protein was extracted with three volumes 100 mM sodium pyrophosphate, 5 mM EGTA, 1 mM dithiothreitol (pH 8.5) diluted with glycerol 1:1 (vol/vol) and were stored at –80˚C until analysis. Myofibrils containing 0.5 µg of protein were loaded on the gel after being incubated for 10 min at 65˚C in sample buffer containing 62.5 mM Tris-HCl, pH 6.8, 20% (vol/vol) glycerol, 5% (vol/vol) β-mercaptoethanol, 2.0% SDS, 0.05% bromphenol blue [
All gels were stained with silver [
Descriptive values are presented as means (standard error (SE). The Pearson correlation coefficient was used to quantify association. The two-sample t-test was conducted to determine differences in the proportion of titin between muscles from the Dex and Contr groups. Linear regression models of ODI and loading volume were estimated to compare the Dex and Contr groups with respect to the ratio of the slopes. In addition, the ratios of the ODI values (titin/MHC, nebulin/MHC) were determined to analyse the differences between the two groups. The significance level used in the analyses was 0.05.
After 10 days of dexamethasone treatment, the wet weight and hind-limb grip strength of Dex group was significantly lower than that in the age-matched Contr group (
After 10 days of dexamethasone infusion, muscle viscoelastic properties of Dex group were significantly different from Contr group (
Elasticity is the ability of the muscle to recover its shape, characterised by the logarithmic decrement of the damped oscillations. The smaller the value of decrement, the more elastic is the tissue. The decrement was significantly higher in the atrophied Gas muscle in Dex group than in Contr group. In addition, the value of decrement correlated positively with the degree of atrophy (r = 0.79
**Significant difference (P < 0.001) between groups.
*Significant difference (P < 0.05) between groups.
P < 0.05) (
Stiffness reflects the resistance of the tissue to the force that changes its shape. In Dex group, stiffness was significantly lower than in Contr group.
Tissue tone is a biomechanical property of the tissue, which can be characterised by two main parameters: stiffness and elasticity. A higher oscillation frequency indicated higher tone. The tone was significantly higher in Dex group than in Contr group.
Titin, nebulin and total MHC were separated using the 2.8% - 12% SDS-PAGE minigel system. No significant changes were seen in the titin isoforms (T1 and T2) composition after dexamethasone treatment compared to Contr group.
The relationship between loading volume and ODI for titin, nebulin, and MHC was determined by linear regression analysis. The slopes ratio of the ODI/loading volume curve (Dex/Cont) for MHC decreased by 17.7%, while the magnitude was more pronounced for titin and nebulin (23.6% and 29.4% respectively).
The densitometric gel analysis revealed differences in the titin to MHC ratio (titin/MHC), nebulin to MHC ratio (nebulin/MHC) and nebulin to titin ratio (nebulin/titin) between the groups (
MHC isoforms composition of the EDL muscle was determined by 8% SDS-PAGE. We observed significant differences in all MHC isoforms between groups (
content of MHC IIb isoform in this muscle (
Muscle viscoelastic properties illustrate muscle state and function in normal and pathological conditions. The present study examined muscle viscoelastic properties in atrophied muscle using a non-invasive electro-mechanical device—myotonometer. Our results showed that the elasticity was lower and the tone higher in atrophied muscle than in normal muscle of Contr group. Lower elasticity was accompanied by the lower content of titin and nebulin in atrophied muscle. It has been shown previously that titin has two isoforms: an isoform of higher molecular weight (T1) and one of lower molecular weight (T2). The latter isoform is considered to be a degradation product of intact titin [
The results showed that the higher the degree of muscle atrophy, the lower the muscle elasticity and the relative content of the MHC IIb isoform in atrophied muscle. The increased muscle tone that was observed in atrophied muscle might be related to changes in the innervation of the muscle, particularly in fast-twitch muscle fibres. Ultrastructural studies have shown that in atrophied muscle, neuromuscular synapses are destroyed in fasttwitch fibres [
Our results showed that the relative content of both titin and MHC decreased to the same degree in atrophied muscle. Therefore, the ratio between titin and MHC remained similar in atrophied muscle to that observed in the control group. It has been shown previously that the content of both titin and myosin is reduced in muscles
*Significant difference (P < 0.05) between groups.
treated with dexamethasone [4,5,14]. The decreased ratio between nebulin and MHC in atrophied muscle indicated that nebulin declined to a greater extent than titin. Taking into account the decreased hind-limb grip strength in the Dex group, there is evidence to suggest that a reduction in the contractile protein myosin and in the elastic proteins of the muscle, including nebulin, might reduce muscle elasticity and the generation of tension. This will impair the ability of the atrophied muscle to store and recover elastic energy.
These findings suggest that glucocorticoid-induced muscle atrophy is accompanied by reduced elasticity and increased tone and stiffness, with concomitant changes in cytoskeletal proteins (titin, nebulin) and contractile protein (myosin) content.
Our results should provide important information for evaluation of musculoskeletal status in case of musculoskeletal disorders.
This study was supported by funding from the Ministry of Education and Research of Estonia, research project number TKKSB1787.