scholarly journals Strain, Muscle Length and Work Output in a Crab Muscle

1989 ◽  
Vol 145 (1) ◽  
pp. 45-61 ◽  
Author(s):  
ROBERT K. JOSEPHSON ◽  
STOKES R. DARRELL

The relationships between muscle length, fractional change in length (strain) and work output during cyclic contraction were examined in scaphognathite levator muscle L2B of the green crab Carcinus maenas (L.). The muscle was subjected to sinusoidal strain at 2 Hz and to phasic stimulation in the strain cycle. At an average length and stimulus phase which are optimum for net work output, the work from muscle L2B during shortening rises to a peak or a plateau with increasing strain. The failure of shortening work to increase continuously with strain is due, in part, to the greater shortening velocity associated with greater strain, and to the consequent reduction in muscle force during shortening at higher velocity. The work required to re-lengthen a muscle following contraction is a complex function of strain, with an initial peak followed by a work minimum and then a monotonic rise in work with further increase in strain. The early work minimum is a result of shortening inactivation which reduces muscle force and thus the work which must be done to re-lengthen the muscle. Because shortening work rises to a peak or plateau with increasing strain while lengthening work, for the most part, increases with strain, there is a sharp optimum strain (about 8%) for net work output. Muscle relaxation becomes slower with increasing muscle length. As muscle length is increased, fusion of tension from cycle to cycle becomes more pronounced and shortening inactivation becomes a more important determinant of optimum strain.

2006 ◽  
Vol 06 (03) ◽  
pp. 229-239 ◽  
Author(s):  
KARL DAGGFELDT

A biomechanical model was generated in order to investigate the possible mechanisms behind reductions in muscle performance due to muscle bulging. It was shown that the proportion of fiber force contributing to the total muscle force is reduced with fiber bulging and that the cause of this reduction is due to the intramuscular pressure (IMP) created by the bulging fibers. Moreover, it was established that the amount of IMP generated muscle force reduction is determined by the extent to which muscle thickening restricts muscle fibers from shortening, thereby limiting their power contribution. It was shown that bulging can set a limit to the maximal size a muscle can take without losing force and power producing capability. Possible effects, due to bulging, on maximal muscle force in relation to both muscle length and muscle shortening velocity were also demonstrated by the model.


1999 ◽  
Vol 202 (18) ◽  
pp. 2551-2565 ◽  
Author(s):  
R.K. Josephson ◽  
D.R. Stokes

Active shortening of respiratory muscle L2B from the crab Carcinus maenas results in contractile deactivation, seen as (1) a decline of force during the course of isovelocity shortening, (2) a reduction in the rate of force redevelopment following shortening, (3) a depression of the level of isometric force reached following shortening, and (4) an accelerated relaxation at the end of stimulation. The degree of deactivation increases with increasing distance of shortening, decreases with increasing shortening velocity, and is approximately linearly related to the work done during shortening. Deactivation lasts many seconds if stimulation is maintained, but is largely although not completely removed if the stimulation is temporarily interrupted so that the force drops towards the resting level. Deactivation for a given distance and velocity of shortening increases with increasing muscle length above the optimum length for force production. Stimulating muscle L2B at suboptimal frequencies gives tetanic contractions that are fully fused but of less than maximal amplitude. The depression of force following shortening, relative to the force during an isometric contraction, is independent of the stimulus frequency used to activate the muscle, indicating that deactivation is not a function of the background level of stimulus-controlled muscle activation upon which it occurs. Deactivation reduces the work required to restretch a muscle after it has shortened, but it also lowers the force and therefore the work done during shortening. The net effect of deactivation on work output over a full shortening/lengthening cycle is unknown.


2019 ◽  
Vol 286 (1903) ◽  
pp. 20190719 ◽  
Author(s):  
André Tomalka ◽  
Oliver Röhrle ◽  
June-Chiew Han ◽  
Toan Pham ◽  
Andrew J. Taberner ◽  
...  

Force enhancement (FE) is a phenomenon that is present in skeletal muscle. It is characterized by progressive forces upon active stretching—distinguished by a linear rise in force—and enhanced isometric force following stretching (residual FE (RFE)). In skeletal muscle, non-cross-bridge (XB) structures may account for this behaviour. So far, it is unknown whether differences between non-XB structures within the heart and skeletal muscle result in deviating contractile behaviour during and after eccentric contractions. Thus, we investigated the force response of intact cardiac trabeculae during and after isokinetic eccentric muscle contractions (10% of maximum shortening velocity) with extensive magnitudes of stretch (25% of optimum muscle length). The different contributions of XB and non-XB structures to the total muscle force were revealed by using an actomyosin inhibitor. For cardiac trabeculae, we found that the force–length dynamics during long stretch were similar to the total isometric force–length relation. This indicates that no (R)FE is present in cardiac muscle while stretching the muscle from 0.75 to 1.0 optimum muscle length. This finding is in contrast with the results obtained for skeletal muscle, in which (R)FE is present. Our data support the hypothesis that titin stiffness does not increase with activation in cardiac muscle.


1987 ◽  
Vol 131 (1) ◽  
pp. 265-287 ◽  
Author(s):  
ROBERT K. JOSEPHSON ◽  
DARRELL R. STOKES

1. Contraction of scaphognathite muscle L2B of the green crab Carcinus maenas is strongly dependent on stimulus number and frequency. Single, supramaximal stimuli evoke little or no tension. When stimulated with shocks in either short bursts (10 stimuli in 0.5s or less) or long bursts (5 s of stimulation), the isometric tension from the muscle increases with increasing stimulus frequency to a maximum at about 150 Hz at 15°C, beyond which tension declines with further increase in stimulus frequency. 2. There can be facilitation of both contraction and relaxation between short bursts of stimuli. Facilitation of contraction is seen as increasing tension on successive bursts of a series, even when the interburst interval is long enough for relaxation to be completed during the interval. Interburst facilitation lasts at least 10 s. Facilitation of relaxation is seen as progressively faster relaxation from burst to burst of a series, and relaxation to lower tension levels when the interburst interval is so short that relaxation is incomplete in the interburst interval. 3. Maximum isometric tension occurs at muscle lengths slightly longer than the longest muscle length reached in vivo. Tension declines rapidly with changes in muscle length away from the optimum length. The maximum isometric tension was about 12 N cm−2. 4. The maximum shortening velocity of a tetanically activated muscle was determined as 1.9 lengthss−1 (Ls−1) by extrapolation of force-velocity curves to zero force and 3.3 Ls−1 by slack test measurements. 5. The scaphognathite muscle would be classified as a slow or tonic muscle on the basis of its requirements for multiple stimulation to reach full activation, and as a moderately fast muscle on the basis of its force-velocity properties.


1995 ◽  
Vol 198 (10) ◽  
pp. 2221-2227 ◽  
Author(s):  
D A Syme ◽  
R K Josephson

The work capacity of segments of atrial and ventricular muscle from the frog Rana pipiens was measured as a function of muscle length using the work loop technique. Both the work done during shortening and the work required to re-lengthen the muscle after shortening increased with muscle length. Net work increased with length up to a maximum, beyond which work declined. The optimum sarcomere length for work output was 2.5-2.6 microns for both atrial and ventricular muscle. Isometric force increased with muscle length to lengths well beyond the optimum for work output. Thus, the decline in work at long lengths is not simply a consequence of a reduction in the capacity of heart muscle to generate force. It is proposed that it is the non-linear increase in work required to re-lengthen muscle with increasing muscle length which limits net work output and leads to a maximum in the relationship between net work and muscle length. Extension of the results from muscle strips to intact hearts suggests that the work required to fill the ventricle exceeds that available from atrial muscle at all but rather short ventricular muscle lengths.


2013 ◽  
Vol 70 (12) ◽  
pp. 1124-1131 ◽  
Author(s):  
Boban Djordjevic ◽  
Marijan Novakovic ◽  
Milan Milisavljevic ◽  
Sasa Milicevic ◽  
Aleksandar Malikovic

Background/Aim. The detailed knowledge of the architecture of the upper eyelid is very important in numerous upper eyelid corrective surgeries. The article deals with the detailed anatomy of the major components of the upper lid, which are commonly seen in surgical practice. Methods. This study was conducted on 19 human cadavers (12 adults and 7 infants) without pathologic changes in the orbital region and eyelids. Anatomic microdissection of the contents of the orbita was performed bilaterally on 12 orbits from 6 unfixed cadavers (3 male and 3 female). Micromorphologic investigations of the orbital tissue were performed on 8 en bloc excised and formalin-fixed orbits of infant cadavers. Specimens were fixed according to the Duvernoy method. An intra-arterial injection of 5% mixture of melt formalin and black ink was administered into the carotid arterial system. Using routine fixation, decalcination, dehydration, illumination, impregnation and molding procedures in paraplast, specimens were prepared for cross-sections. Results. The measurement of the muscle length and diameter in situ in 6 nonfixed cadavers (12 orbits) showed an average length of the levator palpbrae superioris (LPS) muscle body of the 42.0 ? 1.41 mm on the right, and 40.3 ? 1.63 mm on the left side. In all the cases, the LPS had blood supply from 4 different arterial systems: the lacrimal, supratrochlear, and supraorbital artery and muscle branches of the ophthalmic artery. The LPS muscle in all the specimens was supplied by the superior medial branch of the oculomotor nerve. The connective tissue associated with the LPS muscle contains two transverse ligaments: the superior (Whitnall?s) and intermuscular transverse ligaments (ITL). The orbital septum in all the specimens originated from the arcus marginalis of the frontal bone, and consisted of two layers - the superficial and the inner layer. In addition, a detailed histological analysis revealed that the upper eyelid?s crease was formed by the conjoined fascia including the fascia of the orbicularis muscle, the superficial layer of the orbital septum, and the aponeurosis of the LPS muscle, as well as the pretarsal fascia. Conclusion. The conducted study provided a valuable morphological basis for biomechanical and clinical considerations regarding blepharoptosis surgery.


1995 ◽  
Vol 198 (4) ◽  
pp. 975-987 ◽  
Author(s):  
A C Guimaraes ◽  
W Herzog ◽  
T L Allinger ◽  
Y T Zhang

The relationship between force and electromyographic (EMG) signals of the cat soleus muscle was obtained for three animals during locomotion at five different speeds (154 steps), using implanted EMG electrodes and a force transducer. Experimentally obtained force-IEMG (= integrated EMG) relationships were compared with theoretically predicted instantaneous activation levels calculated by dividing the measured force by the predicted maximal force that the muscle could possibly generate as a function of its instantaneous contractile conditions. In addition, muscular forces were estimated from the corresponding EMG records exclusively using an adaptive filtering approach. Mean force-IEMG relationships were highly non-linear but similar in shape for different cats and different speeds of locomotion. The theoretically predicted activation-time plots typically showed two peaks, as did the IEMG-time plots. The first IEMG peak tended to be higher than the second one and it appeared to be associated with the initial priming of the muscle for force production at paw contact and the peak force observed early during the stance phase. The second IEMG peak appeared to be a burst of high muscle activation, which might have compensated for the levels of muscle length and shortening velocity that were suboptimal during the latter part of the stance phase. Although it was difficult to explain the soleus forces on the basis of the theoretically predicted instantaneous activation levels, it was straightforward to approximate these forces accurately from EMG data using an adaptive filtering approach.


2000 ◽  
Vol 203 (17) ◽  
pp. 2667-2689 ◽  
Author(s):  
R.K. Josephson ◽  
J.G. Malamud ◽  
D.R. Stokes

The basalar muscle of the beetle Cotinus mutabilis is a large, fibrillar flight muscle composed of approximately 90 fibers. The paired basalars together make up approximately one-third of the mass of the power muscles of flight. Changes in twitch force with changing stimulus intensity indicated that a basalar muscle is innervated by at least five excitatory axons and at least one inhibitory axon. The muscle is an asynchronous muscle; during normal oscillatory operation there is not a 1:1 relationship between muscle action potentials and contractions. During tethered flight, the wing-stroke frequency was approximately 80 Hz, and the action potential frequency in individual motor units was approximately 20 Hz. As in other asynchronous muscles that have been examined, the basalar is characterized by high passive tension, low tetanic force and long twitch duration. Mechanical power output from the basalar muscle during imposed, sinusoidal strain was measured by the work-loop technique. Work output varied with strain amplitude, strain frequency, the muscle length upon which the strain was superimposed, muscle temperature and stimulation frequency. When other variables were at optimal values, the optimal strain for work per cycle was approximately 5%, the optimal frequency for work per cycle approximately 50 Hz and the optimal frequency for mechanical power output 60–80 Hz. Optimal strain decreased with increasing cycle frequency and increased with muscle temperature. The curve relating work output and strain was narrow. At frequencies approximating those of flight, the width of the work versus strain curve, measured at half-maximal work, was 5% of the resting muscle length. The optimal muscle length for work output was shorter than that at which twitch and tetanic tension were maximal. Optimal muscle length decreased with increasing strain. The curve relating work output and muscle length, like that for work versus strain, was narrow, with a half-width of approximately 3 % at the normal flight frequency. Increasing the frequency with which the muscle was stimulated increased power output up to a plateau, reached at approximately 100 Hz stimulation frequency (at 35 degrees C). The low lift generated by animals during tethered flight is consistent with the low frequency of muscle action potentials in motor units of the wing muscles. The optimal oscillatory frequency for work per cycle increased with muscle temperature over the temperature range tested (25–40 degrees C). When cycle frequency was held constant, the work per cycle rose to an optimum with increasing temperature and then declined. We propose that there is a temperature optimum for work output because increasing temperature increases the shortening velocity of the muscle, which increases the rate of positive work output during shortening, but also decreases the durations of the stretch activation and shortening deactivation that underlie positive work output, the effect of temperature on shortening velocity being dominant at lower temperatures and the effect of temperature on the time course of activation and deactivation being dominant at higher temperatures. The average wing-stroke frequency during free flight was 94 Hz, and the thoracic temperature was 35 degrees C. The mechanical power output at the measured values of wing-stroke frequency and thoracic temperature during flight, and at optimal muscle length and strain, averaged 127 W kg(−1)muscle, with a maximum value of 200 W kg(−1). The power output from this asynchronous flight muscle was approximately twice that measured with similar techniques from synchronous flight muscle of insects, supporting the hypothesis that asynchronous operation has been favored by evolution in flight systems of different insect groups because it allows greater power output at the high contraction frequencies of flight.


1978 ◽  
Vol 235 (1) ◽  
pp. C20-C24 ◽  
Author(s):  
J. A. Rall

It has been proposed that the energy (heat + work) output of an isometric twitch is determined by the force that is generated under conditions of invariant activation, irrespective of muscle length. To test the effect of length and force on total energy output, muscles were stretched by increments beyond the muscle length at which twitch force is maximum (LO) and then stimulated; energy output and force then were measured. These data were compared with isovelocity twitches in which stimulated muscles, initially at different lengths, shortened (near maximum velocity) a constant distance and then redeveloped tension at lengths less than LO. If energy liberation was determined by force generation, plots of energy output versus force produced would be parallel with isovelocity twitches liberating extra energy as shortening heat. As predicted, the ratio of the slopes (n = 13) of these relations, 0.98 +/- 0.02, was not different from 1 and the shortening heat coefficient (alphaF/Pot, measured from the difference in intercepts), 0.15 +/- 0.01, was near to the expected value. Therefore, energy liberation in twitches appears to be uniquely determined by force generation and not by muscle length.


1988 ◽  
Vol 64 (5) ◽  
pp. 2053-2057 ◽  
Author(s):  
C. Y. Seow ◽  
N. L. Stephens

Zero-load velocity (V0) as a function of the length of canine tracheal smooth muscle was obtained by applying zero-load clamps to isotonically contracting muscle under various loads. The load clamps were applied at a specific time after onset of contraction. The magnitude of the isotonic load therefore determines the length of the muscle at the moment of release or at the moment the unloaded shortening velocity was measured. A family of such V0-muscle length (L) curves was obtained at 1-s intervals in the time course of contraction. The V0-L curve was fitted by a parabolic function with satisfactory goodness of fit. The maximum shortening velocity at optimum muscle length varied with time, but the minimum length at which V0 diminished to zero was time independent.


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