Superficial Abdominal Muscles Research Articles

Differential control of abdominal muscles during multi-directional support-surface translations in man

The current study aimed to understand how deep and superficial abdominal muscles are coordinated with respect to activation onset times and amplitudes in response to unpredictable support-surface translations delivered in multiple directions. Electromyographic (EMG) data were recorded intra-muscularly using fine-wire electrodes inserted into the right rectus abdominis (RA), obliquus externus (OE), obliquus internus (OI) and transversus abdominis (TrA) muscles. Twelve young healthy male subjects were instructed to maintain their standing balance during 40 support surface translations (peak acceleration 1.3 m s(-2); total displacement 0.6 m) that were counter-balanced between four different directions (forward, backward, leftward, rightward). Differences between abdominal muscles in EMG onset times were found for specific translation directions. The more superficial RA (backward translations) and OE (forward and leftward translations) muscles had significantly earlier EMG onsets compared to TrA. EMG onset latencies were dependent on translation direction in RA, OE and OI, but independent of direction in TrA. EMG amplitudes in RA and OE were dependent on translation direction within the first 100 ms of activity, whereas responses from the two deeper muscles (TrA and OI) were independent of translation direction during this interval. The current results provide new insights into how abdominal muscles contribute to postural reactions during human stance. Response patterns of deep and superficial abdominal muscles during support surface translations are unlike those previously described during upper-body perturbations or voluntary arm movements, indicating that the neural mechanisms controlling individual abdominal muscles are task-specific to different postural demands.

Designing an ultrasonic motion analysis system for new method of clinical evaluation of axial body segments stabilization during dynamic conditions

Objective: To study the EMG activity of selected trunk muscles during self-initiated voluntary flexion and extension of the trunk in post-stroke hemiparetic subjects, and to compare measurement results to corresponding findings in control subjects.Methods: Using a sample of 50 patients and 30 control subjects, bilateral EMG activity of the rectus abdominis (RA) and external oblique (EO) muscles was studied during direct trunk flexion, and activity of the lumbar erector spinae (ES) and latissimus dorsi (LD) was studied during straight trunk extension. Variables of timing, magnitude, and temporal synchronization between muscle activity on the paretic and non-paretic sides of the body in the patient group were compared with the same measurements taken from the left and right sides of the body in the control group.Results: Activity of the RA and LD muscles on the affected side of the body was reduced and delayed relative to the unaffected side in the patients and relative to the control subjects. Some deterioration was also observed in the function of the EO muscle, whereas the lumbar ES displayed normal activity on both sides of the body. Trunk velocity during both flexion and extension was slower in the patients than in the controls.Conclusions: Despite the existence of ipsilateral as well as contralateral higher inputs to axial and to a lesser extent also to more lateral trunk muscles, the function of the superficial abdominal muscles and of the LD muscle is adversely affected by a contralateral stroke. Conversely, the lumbar ES, which can be categorized as local trunk extensors, seem to normally fulfill their anti-gravitational task on both sides of the body.

7.3 Postural reactions in deep and superficial abdominal muscles to support-surface translations: The effect of expectation

7.3 Postural reactions in deep and superficial abdominal muscles to support-surface translations: The effect of expectation

Electromyographic activity of voluntarily activated trunk flexor and extensor muscles in post-stroke hemiparetic subjects.

To study the EMG activity of selected trunk muscles during self-initiated voluntary flexion and extension of the trunk in post-stroke hemiparetic subjects, and to compare measurement results to corresponding findings in control subjects. Using a sample of 50 patients and 30 control subjects, bilateral EMG activity of the rectus abdominis (RA) and external oblique (EO) muscles was studied during direct trunk flexion, and activity of the lumbar erector spinae (ES) and latissimus dorsi (LD) was studied during straight trunk extension. Variables of timing, magnitude, and temporal synchronization between muscle activity on the paretic and non-paretic sides of the body in the patient group were compared with the same measurements taken from the left and right sides of the body in the control group. Activity of the RA and LD muscles on the affected side of the body was reduced and delayed relative to the unaffected side in the patients and relative to the control subjects. Some deterioration was also observed in the function of the EO muscle, whereas the lumbar ES displayed normal activity on both sides of the body. Trunk velocity during both flexion and extension was slower in the patients than in the controls. Despite the existence of ipsilateral as well as contralateral higher inputs to axial and to a lesser extent also to more lateral trunk muscles, the function of the superficial abdominal muscles and of the LD muscle is adversely affected by a contralateral stroke. Conversely, the lumbar ES, which can be categorized as local trunk extensors, seem to normally fulfill their anti-gravitational task on both sides of the body.

Tubular localization of silent calcium channels in crustacean skeletal muscle fibers.

Ca2+-induced Ca2+ release (CICR) in the superficial abdominal flexor muscle of the crustacean Atya lanipes appears to be mediated by a local control mechanism similar to that of vertebrate cardiac muscle, but with an unusually high gain. Thus, Ca2+ influx increases sufficiently the local concentration of Ca2+ in the immediate vicinity of the sarcoplasmic reticulum Ca2+ release channels to trigger the highly amplified release of Ca2+ required for contraction, but is too low to generate a macroscopic inward current (i.e., the Ca2+ channels are silent). To determine the localization of the silent Ca2+ Channels, the mechanical, electrophysiological and ultrastructural properties of the muscle were examined before and after formamide treatment, a procedure that produces the disruption of transverse tubules of striated muscle. We found that tubular disruption decreased tension generation by about 90%; reduced inward current (measured as Vmax, the maximum rate of rise of Sr2+ action potentials) by about 80%; and decreased membrane capacitance by about 77%. The results suggest that ca. 80% of the silent Ca2+ channels are located in the tubular system. Thus, these studies provide further evidence to support the local control mechanism of CICR in crustacean skeletal muscle.

Trunk muscle fatigue during a back extension task in standing

There is some evidence that the fatiguing characteristics during isometric back extension tasks may assist in identifying differences between individuals with and without low back pain (LBP). During these tasks, especially in standing, other abdominal trunk muscles are also active. The abdominal trunk muscles acting across multiple segments of the lumbar spine function in isolation or in synergy to create flexion torques. It is suggested that co-activation patterns of the trunk muscles are able to control the axis of rotation of the extension torque and also provide multi-segmental stability of the spine. The purpose of this study was to examine the fatigue responses in 4 asymptomatic individuals to a sustained isometric extension task of the trunk muscles evaluating the shifts in the median frequency of the electromyographic (EMG) signal. This study suggests that in asymptomatic subjects, the more superficial abdominal muscles (External Oblique and Rectus Abdominis) increased in activity as the test progressed. There was large inter-individual variation in both amplitude and median frequency changes. Rectus abdominis and the back extensors demonstrated characteristics of fatigue during the task. Studies to test for any characteristic trends in whether specific trunk muscles fatigue in standing is a feature in chronic LBP, invites a formal investigation.

Changes in motor planning of feedforward postural responses of the trunk muscles in low back pain.

Changes in trunk muscle recruitment have been identified in people with low-back pain (LBP). These differences may be due to changes in the planning of the motor response or due to delayed transmission of the descending motor command in the nervous system. These two possibilities were investigated by comparison of the effect of task complexity on the feedforward postural response of the trunk muscles associated with rapid arm movement in people with and without LBP. Task complexity was increased by variation of the expectation for a command to either abduct or flex the upper limb. The onsets of electromyographic activity (EMG) of the abdominal and deltoid muscles were measured. In control subjects, while the reaction time of deltoid and the superficial abdominal muscles increased with task complexity, the reaction time of transversus abdominis (TrA) was constant. However, in subjects with LBP, the reaction time of TrA increased along with the other muscles as task complexity was increased. While inhibition of the descending motor command cannot be excluded, it is more likely that the change in recruitment of TrA represents a more complex change in organisation of the postural response.

Muscle type-specific myosin isoforms in crustacean muscles

Differential expression of multiple myosin heavy chain (MyHC) genes largely determines the diversity of critical physiological, histochemical, and enzymatic properties characteristic of skeletal muscle. Hypotheses to explain myofiber diversity range from intrinsic control of expression based on myoblast lineage to extrinsic control by innervation, hormones, and usage. The unique innervation and specialized function of crayfish (Procambarus clarkii) appendicular and abdominal musculature provide a model to test these hypotheses. The leg opener and superficial abdominal extensor muscles are innervated by tonic excitatory motoneurons. High resolution SDS-PAGE revealed that these two muscles express the same MyHC profile. In contrast, the deep abdominal extensor muscles, innervated by phasic motoneurons, express MyHC profiles different from the tonic profiles. The claw closer muscles are dually innervated by tonic and phasic motoneurons and a mixed phenotype was observed, albeit biased toward the phasic profile seen in the closer muscle. These results indicate that multiple MyHC isoforms are present in the crayfish and that differential expression is associated with diversity of muscle type and function.

Silent calcium channels in skeletal muscle fibers of the crustacean Atya lanipes.

The superficial (tonic) abdominal flexor muscles of Atya lanipes do not generate Ca(2+) action potentials when depolarized and have no detectable inward Ca(2+) current. These fibers, however, are strictly dependent on Ca(2+) influx for contraction, suggesting that they depend on Ca(2+)-induced Ca(2+) release for contractile activation. The nature of the communication between Ca(2+) channels in the sarcolemmal/tubular membrane and Ca(2+) release channels in the sarcoplasmic reticulum in this crustacean muscle was investigated. The effects of dihydropyridines on tension generation and the passive electrical response were examined in current-clamped fibers: Bay K 8644 enhanced tension about 100% but did not alter the passive electrical response; nifedipine inhibited tension by about 70%. Sr(2+) and Ba(2+) action potentials could be elicited in Ca(2+)-free solutions. The spikes generated by these divalent cations were abolished by nifedipine. As the Sr(2+) or Ba(2+) concentrations were increased, the amplitudes of the action potentials and their maximum rate of rise, V(max), increased and tended towards saturation. Three-microelectrode voltage-clamp experiments showed that even at high (138 mm) extracellular Ca(2+) concentration the channels were silent, i.e., no inward Ca(2+) current was detected. In Ca(2+)-free solutions, inward currents carried by 138 mm Sr(2+) or Ba(2+) were observed. The currents activated at voltages above -40 mV and peaked at about 0 mV. This voltage-activation profile and the sensitivity of the channels to dihydropyridines indicate that they resemble L-type Ca(2+) channels. Peak inward current density values were low, ca. -33 microA/cm(2) for Sr(2+) and -14 microA/cm(2) for Ba(2+), suggesting that Ca(2+) channels are present at a very low density. It is concluded that Ca(2+)-induced Ca(2+) release in this crustacean muscle operates with an unusually high gain: Ca(2+) influx through the silent Ca(2+) channels is too low to generate a macroscopic inward current, but increases sufficiently the local concentration of Ca(2+) in the immediate vicinity of the sarcoplasmic reticulum Ca(2+) release channels to trigger the highly amplified release of Ca(2+) required for tension generation.

Muscle type–specific myosin isoforms in crustacean muscles

Differential expression of multiple myosin heavy chain (MyHC) genes largely determines the diversity of critical physiological, histochemical, and enzymatic properties characteristic of skeletal muscle. Hypotheses to explain myofiber diversity range from intrinsic control of expression based on myoblast lineage to extrinsic control by innervation, hormones, and usage. The unique innervation and specialized function of crayfish (Procambarus clarkii) appendicular and abdominal musculature provide a model to test these hypotheses. The leg opener and superficial abdominal extensor muscles are innervated by tonic excitatory motoneurons. High resolution SDS-PAGE revealed that these two muscles express the same MyHC profile. In contrast, the deep abdominal extensor muscles, innervated by phasic motoneurons, express MyHC profiles different from the tonic profiles. The claw closer muscles are dually innervated by tonic and phasic motoneurons and a mixed phenotype was observed, albeit biased toward the phasic profile seen in the closer muscle. These results indicate that multiple MyHC isoforms are present in the crayfish and that differential expression is associated with diversity of muscle type and function. J. Exp. Zool. 286:36–48, 2000. © 2000 Wiley-Liss, Inc.

Transversus abdominis and the superficial abdominal muscles are controlled independently in a postural task

By manipulation of movement reaction time we investigated the co-ordination between the motor command for arm movement and the associated ‘anticipatory’ postural response of the abdominal muscles. Limb movement reaction time was varied by changing the expectation of limb movement direction required in a choice-reaction-time task. Timing of the ‘anticipatory’ postural contraction of transversus abdominis (TrA) was invariant while the limb movement reaction time varied with changes in expectation of required response. In contrast, the timing of ‘anticipatory’ postural activity of the other abdominal muscles co-varied with limb movement reaction time. Dissociation of the behaviour of TrA and the other abdominal muscles suggests that TrA may be controlled independently of the motor command for limb movement in contrast to the other abdominal muscles.

Shortening properties of two biochemically defined muscle fibre types of the Norway lobster Nephrops norvegicus L.

Mechanical properties of myofibrillar bundles from single chemically skinned fibres from the superficial abdominal flexor muscle of the Norway lobster Nephrops norvegicus were measured, and the protein content of these fibres was analysed by SDS-PAGE. Two slow fibre phenotypes (S1, S2) were distinguished on the basis of their myofibrillar protein assemblages. Data from 9 S1 and 8 S2 fibres obtained at similar sarcomere length demonstrate significant differences between the fibre types in maximal tension (N cm-2, S1: 10.5 +/- 3.9; S2: 3.1 +/- 0.8), in the delay of the peak of stretch activation (ms, S1: 122 +/- 18; S2: 412 +/- 202), in fibre stiffness (N cm-2 per nm half sarcomere, S1: 0.36 +/- 0.19; S2: 0.09 +/- 0.03) and in maximal shortening velocity (fibre length s-1, S1: 0.53 +/- 0.10; S2: 0.27 +/- 0.06). Furthermore, the maximal power output of the type S1 fibres was about five times larger than that of S2 fibres. The power output was maximal at lower loads in S1 fibres (relative load = 0.37 +/- 0.04) than in S2 fibres (relative load = 0.44 +/- 0.05). This study represents a comprehensive investigation of two slow muscle fibre types which are thought to be specialized for slow movements (S1 fibres) and for the postural control of the abdomen (S2 fibres).

Distribution and morphology of inhibitory innervation in crayfish ( Procambarus clarkii ) limb and abdominal muscles

The general morphology and distribution of inhibitory nerve terminals in representative limb and abdominal muscles of the crayfish (Procambarus clarkii) were studied by using a polyclonal antiserum against conjugated gamma-aminobutyric acid. A double-labelling procedure with gamma-aminobutyric acid and synaptotagmin antisera was employed to study the relationship between inhibitory and excitatory innervation. The neuromuscular junctions were visualized with confocal scanning laser microscopy. Two morphologically distinct types of inhibitory nerve ending were observed. In the leg opener and superficial abdominal flexor muscles, which are innervated by tonic excitatory motor neurons, the inhibitory terminals were large and distinctly varicose, as were the excitatory motor terminals. In the deep abdominal extensor muscle, which is supplied by phasic excitatory motor neurons, the inhibitory terminals, like the excitatory terminals, were slender and lacked large varicosities. In the main leg extensor muscle, which receives dual excitatory innervation from phasic and tonic motor neurons, the inhibitory terminals had the varicose morphology characteristic of tonic excitatory terminals. The inhibitory motor axons branched closely in parallel with the excitatory motor axons in the leg opener and abdominal flexor muscles, whereas in the main leg and deep abdominal extensor muscles, many preterminal and terminal branches of the excitatory neurons were unaccompanied by inhibitory innervation. Inhibitory terminal morphology is consistent with the physiological phenotype of these neurons.

Calcium-activated and stretch-induced force responses in two biochemically defined muscle fibre types of the Norway lobster.

Mechanical properties of thin (< 80 microns) myofibrillar bundles from single rehydrated freeze-dried fibres of the superficial abdominal flexor muscle of the lobster Nephrops norvegicus have been measured, and subsequently the protein content of these fibres has been analysed by SDS-PAGE. Two slow fibre phenotypes can be distinguished on the basis of their myofibrillar assemblages and sarcomere length (type S1: 6.0-7.5 microns, type S2: 8.0-10.9 microns). Differences (means +/- SD, average of seven fibres of each type) were observed in the kinetics for Ca2+ activation (half time of force development (ms); S1: 416 +/- 174; S2: 762 +/- 199 plus a delay of 280 +/- 130) and relaxation (half time of force decay (ms); S1: 162 +/- 75, S2: 257 +/- 53), for Ca2+ sensitivity of force generation (-log [Ca2+] for half maximal activation; S1: 5.40 +/- 0.12; S2: 5.55 +/- 0.08), and of the kinetics of stretch activation (delay of the peak of stretch-induced force increase (ms); S1: 91 +/- 30; S2: 493 +/- 436). From these results and partly also in combination with previously obtained mechanical data on intact fibres it can be concluded (1) that S2 fibres are specialized for long-lasting force maintenance whereas S1 fibres are adapted for slow movements; (2) intrinsic myofibrillar kinetics is not the main time-limiting factor for either activation or relaxation of intact fibres under physiological conditions; (3) processes which precede crossbridge cycling seem to be the main time-limiting factors for the Ca2+ activation of the myofibrils.

Dynamic responses of intra-abdominal pressure and abdominal muscle activity during trunk loading

The present study focuses on the role of superficial abdominal muscles revealed by electromyographic recordings during the maintenance of a bipedal stance perturbed by post-exercise hyperventilation. Twelve healthy subjects performed six 30-s postural tests: one pre-exercise test while breathing quietly, then one test every minute for the 5 min immediately following a maximum-intensity, incremental cycling exercise test. Displacement of the centre of pressure in the sagittal plane was monitored over time. Myoelectric activities of the obliquus externus (OE), obliquus internus (OI) and rectus abdominis (RA) muscles were recorded by surface electromyography (EMG). Metabolic parameters were measured with a portable telemetric device. The change in ventilatory drive induced by exercise was accompanied by a significant increase in both postural sway parameters and EMG activities. For OE and OI, the increased EMG activities were prominent during expiration, whereas OI was silent during inspiration. OE and RA were activated during both expiration and inspiration. It is concluded that the compensation of respiratory disturbances of the erect posture appears to be less effective when minute ventilation increases. The patterns of muscle activity suggest that abdominal muscles are controlled differentially and that their functional coordination is dependent on the respiratory demand.

Mechanics of stretch in activated crustacean slow muscle. I. Factors affecting peak force.

1. The active stiffness of ventral superficial abdominal muscle (VSM) of the hermit crab, Pagurus pollicarus, was measured with ramp stretches of different amplitudes and velocities. Active stiffness was calculated by subtracting the peak force produced by passive stretch and the isometric force just before stretch from the peak force produced by stretching active muscle. The result was then divided by stretch length to give stiffness. 2. The relationship between force just before stretch (the level of activation) and active stiffness was curvilinear and was found to apply under a variety of experiment conditions. For pooled data from eight experiments, active stiffness (GN.m-2.m-1) = 3.2*stress (MN/m2)-7.6*stress2. Decreasing the number of motor units or activating the inhibitor did not alter this relationship nor did the addition of proctolin, octopamine, or 5-HT to the bath. The relationship also applied during the rising phase of isometric tension. However, stiffness declined more rapidly than predicted by this relationship after the end of tetanus. 3. Active stiffness varied inversely with stretch amplitude for fast stretches, and the slope of this relationship increased with increasing muscle activation. At lower stretch velocities, the slope was much less than at rapid stretch velocities, so at low levels of activation and stretch velocity, active stiffness was essentially independent of stretch length. 4. Active stiffness covaried with muscle force as both were sampled at shorter and shorter lengths on the ascending limb of the length-tension curve.(ABSTRACT TRUNCATED AT 250 WORDS)

Veratridine-induced high-frequency asynchronous release of inhibitory transmitter quanta in crayfish nerve-muscle synapses superfused with normal and low-calcium saline.

Crayfish fibres of opener muscles were voltage clamped to E = -80 mV membrane potential (T = 19-22 degrees C), and veratridine (10-100 mumol/l) was added to the superfusate. Within 30-60 s this caused large fluctuations of the clamp current due to vigorous asynchronous quantal release from the inhibitory nerve terminals along the muscle fibre. Excitatory postsynaptic receptors were previously desensitized by application of 5 mmol/l glutamate. Current fluctuations were evaluated by means of the noise analysis technique. Typically, 100 mumol/l veratridine increased instantaneously the quantal release rate n from n less than 1 quantum/s to n congruent to 10,000 quanta/s. Thereafter, n declined exponentially with a time constant of congruent to 70 s. On average, about 500,000 inhibitory quanta could be liberated in this way from the terminals on a single muscle fibre of congruent to 1 mm length. Serotonin (1 mumol/l) facilitated the effect of lower veratridine concentrations (1-10 mumol/l). In opener muscles veratridine-induced asynchronous quantal release showed little dependence on the bath concentration of Ca2+. The opposite was found for fibres of the superficial abdominal extensor muscle. Beside postsynaptic current fluctuations, veratridine elicited slowly changing average postsynaptic DC-currents which could be explained partly by superposition of individual inhibitory quantal currents. These DC-currents suggest that beside inhibitory quantal release another factor activates inhibitory postsynaptic receptors after application of veratridine.

Differential effect of intraterminal sodium on spontaneous quantal release of transmitter in two neuromuscular junctions of crayfish

Nerve terminals on the superficial abdominal extensor muscle and the claw opener muscle of small crayfish were loaded with sodium by bath application of 100 μmol/l veratridine in superfusates where normal Ca 2+ was removed (low-Ca 2+ superfusate). In both preparations this caused an increase in spontaneous quantal release of excitatory and inhibitory transmitter which was evaluated by means of the noise analysis technique. About 2.5 min after application of veratridine, when spontaneous quantal release had largely ceased, the normal Ca 2+ concentration was reestablished. This increased transiently the quantal release rate a second time. However, release activated by Ca 2+ application was much more vigorous at the superficial abdominal extensor muscle than at the claw opener. At the superficial abdominal extensor muscle on average about 8% of the total number of quanta could be released in low Ca 2+ and 92% in normal Ca 2+ superfusate, while at the claw opener 75% of the quanta were released in low Ca 2+ and 25% in normal Ca 2+ superfusate. The experiments suggest that intraterminal sodium has a differential effect in the terminals of the two preparations. Possibly, the intraterminal source from which Na + may liberate Ca 2+ is more restricted in the superficial abdominal extensor muscle than in the opener muscle of the claw.

Diversity of muscle fibers in the abdominal dorsal superficial muscles of the hermit crab,Pagurus pollicarus

The dorsal superficial abdominal muscles of the hermit crab,Pagurus pollicarus, are divided into three subregions of muscle fibers with different properties: a lateral group of tonic muscle fibers and two groups of medial muscle fibers, a superficial layer with intermediate properties and a central layer of twitch fibers. Fast muscles like those in the central medial region are not found in homologous muscles of crayfish and lobster. The number of muscle fibers (74) is the same on the two sides, but there is a tendency for there to be larger fibers on the left side. Length-tension measurements in these muscles resemble results obtained from other crustacean muscles despite their modification as part of a hydrostatic skeletal system. It is concluded that muscle fibers in homologous muscles of different species may vary in their contractile properties, the degree of their segregation into discrete sub-regions, laterality, and number.

Glycogen in Crustacean Fast and Slow Muscles

Ultrastructural examination of crayfish superficial (tonic) and deep (phasic) abdominal extensor muscles reveals a distribution and quantitative difference in glycogen between these muscles. Both superficial and deep fibers have a dense accumulation of glycogen in the interfibrillar sarcoplasm. In addition, the superficial extensors, but not the deep extensors, contain glycogen in the I band region. The glycogen granules are of the β type and can be removed enzymatically. The superficial medial and lateral fibers contain more glycogen than the medial and lateral deep fibers. A possible functional role for this difference is suggested.