Contraction Times Of Units Research Articles

Directions of Torques Produced About the Ankle Joint by Cat Medial Gastrocnemius Motor Units

Differences in the directions of torque produced by motor units might be used by the nervous system to coordinate posture and movement. Here we report plantar flexion and abduction isometric torques exerted at the ankle by 158 motor units in the cat medial gastrocnemius (MG) muscle. In five cats, motor unit torque direction differed by an average of 10°. Torque direction was weakly correlated with unit contraction time in 3 of 5 experiments, with tetanic force in 3 of 5 experiments, and with conduction velocity in 1 of 5 experiments. The direction of whole muscle torque, however, was constant at all levels of MG activation produced in sural and crossed extension reflexes. Thus, although there is a range in the direction of torque produced by motor units in the cat MG, we find no evidence for the ordering of motor units according to torque direction during MG activation.

Neurophysiology of fastest voluntary muscle contraction in hereditary neuropathy

In patients with hereditary motor and sensory neuropathy types I (demyelinative) and II (neuronal) and in normal subjects, isometric force and electromyographic activity of the first dorsal interosseous muscle were recorded during fastest voluntary contractions and during twitches evoked by nerve stimulation. The maximum voluntary force of the first dorsal interosseous muscle was also measured. In patients, fastest voluntary contraction time (i.e., time from onset of contraction to peak force) was prolonged and inversely proportional to maximum voluntary force. Maximum rate of rise of tension (i.e., slope of rise in force) was reduced and directly proportional to maximum voluntary force. In patients with hereditary motor and sensory neuropathy type I, contraction time was longer and the maximum rate of rise of tension was lower than in those with hereditary motor and sensory neuropathy type II. In patients and normal subjects, voluntary contraction time was closely correlated with the duration of electromyographic bursts. In patients, the twitch contraction time was prolonged and inversely proportional to maximum voluntary force. Twitch contraction amplitude was diminished and directly proportional to maximum voluntary force. Neither twitch contraction time nor amplitude were dependent on the type of hereditary motor and sensory neuropathy. Twitch contraction time evoked by proximal nerve stimulation was minimally longer than that evoked by distal stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)

The dynamic response of cat gastrocnemius motor units investigated by ramp-current injection into their motoneurones.

1. The isometric force developed by single motor units in response to injection of ramp-and-hold currents into their motoneurones was recorded from the common tendon of the gastrocnemius muscles of the cat. The average rate of rise of the force (force-slope) produced by the ramp-evoked discharge, was found to grow almost linearly with the rate of current injection (current-slope) up to a saturation value (maximal force-slope). 2. The slope of the function which links the force slope to the current-slope is the gain (dF/dI) of the motor unit under dynamic conditions. The value of the dynamic gain, measured in the linear region of growth, displays a large variability, i.e. for each nanoampere of current injected, the force developed is as much as 40 times larger in the strongest than in the weakest motor units. Such large gain differences, however, are drastically reduced if the force is expressed as a percentage of the maximal tetanic tension, Ft: per nanoampere injected, most of the units deliver from 1.0 to 3.0% of Ft. 3. The maximal force-slope which each unit could reach exhibits a large variability, ranging from 0.06 to 4.0 g ms-1. Like the dynamic gain, the maximal force-slope is positively related to Ft. 4. It was found that the dynamic sensitivity of the motoneurone, i.e. the increase of the firing rate per unitary increase of the current-slope, governs the fractional growth of the force-slope, whereas the motor unit contraction time determines the firing rate at which maximal force-slope is reached. Together, the two factors co-operate in defining, for each motor unit, the range of input-slopes within which the force-slope is regulated. 5. The motoneurones which supply the weak motor units, those with the lowest dynamic gain, have higher dynamic sensitivity and lower rheobase than those innervating the strong motor units. This suggests that weak motor units need less synaptic current both to be recruited and to reach the maximal speed of force development when their input is supraliminal.

Histochemical and physiological properties of cat motor units after self-and cross-reinnervation.

1. This report describes selected histochemical and physiological properties of the motor units of adult cat soleus muscle approximately one year after self- and cross-reinnervation with the nerve of the heterogenous flexor hallucis longus (f.h.l.). Self-reinnervated f.h.l. motor units are also considered. Whole muscles were tested for fibre reaction to alkaline pre-incubated ATPase, alpha-glycerophosphate dehydrogenase (alpha-GPD) and reduced nicotinamide adenine dinucleotide diaphorase (NADH-D). Motor units were isolated and studied by splitting the ventral root in acute preparations.2. The histochemical fibre type profile in the self-reinnervated muscle was comparable to normal muscle as was mean twitch contraction time, twitch-tetanus ratio and fatigue index. The mean tetanic tension of the soleus self- and cross-reinnervated motor units appeared close to a normal soleus whereas the mean tetanic tension of the f.h.l. self-reinnervated units was significantly less than a normal f.h.l.3. An average of 14% of the fibres of the soleus cross-reinnervated muscles had high ATPase and a alpha-GPD staining intensity in contrast to normal and self-reinnervated soleus in which such fibres are absent. Thus alkaline lability of myofibrillar ATPase increased in some fibres of what was originally a homogeneous population. The small increase in the number of densely staining fibres for ATPase at an alkaline pH (14%) was associated with a 73% decrease in (mean) contraction time (41 +/- 11 ms) of the thirty-three cross-reinnervated muscle units studied, with no unit's contraction time greater than 60 ms. Mean contraction times for the self-reinnervated soleus and f.h.l. muscles were 78 +/- 31 ms and 27 +/- 8 ms respectively.4. All fibres of the soleus cross-reinnervated muscles showed intense reaction to NADH-D, as was true of self-reinnervated soleus. This staining pattern is typical of normal soleus. In concordance, these motor units consistently demonstrated a high resistance to fatigue when stimulated for a four-minute period.5. These results suggest that in the adult self-and cross-reinnervated soleus muscle, there is some active mechanism which regulates the eventual size of motor units as reflected by tetanic tension.6. Change in contraction time from that typical for a soleus unit to that similar to an f.h.l. unit remains incomplete one year after cross-reinnervation. Within this time this partial change in single motor units reflects incomplete neural control of this property rather than a mixture of self- and foreign-innervation.7. A greater degree of independence from neural control to conversion of the histochemically demonstrated myofibrillar ATPase activity exists than is the case for contraction time.

Muscle units divided among retractor bulbi muscle slips and between the lateral rectus and retractor bulbi muscles in cat

Single muscle units of the retractor bulbi and lateral rectus muscles were activated with brief (0.5-ms) current pulses delivered through an intracellular micropipet penetrating single motoneuron cell bodies or axons in the principal abducens nucleus of the cat. Muscle unit mechanical characteristics were measured. A total of 40 retractor bulbi muscle units was studied. Thirty muscle units were contained in 2, 3, or all 4 retractor bulbi muscle slips. Three muscle units involved one retractor bulbi muscle slip and seven units were contained in the lateral rectus muscle plus one or both of the lateral retractor bulbi muscle slips. The largest percentage of muscle units (32.5%) was contained in the two inferior retractor bulbi muscle slips. The 33 retractor bulbi muscle units, having no muscle fibers in the lateral rectus muscle, caused the contraction of 76 retractor bulbi muscle slips. Twitch tension was measured in 58 slips and maximum tetanic tension in 27 slips. The average twitch tension per measured slip was 68.0 mg and the average maximum tetanic tension was 459.8 mg. The average retractor bulbi muscle unit contraction time was 10 ms and the lateral rectus average contraction time was 7.9 ms. We propose that peripheral branching of abducens nerve axons can account for the division of muscle unit components among the retractor bulbi muscle slips and between the lateral rectus and retractor bulbi muscles.

Post-tetanic potentiation of twitch motor units in snake costocutaneous muscle.

1. Isometric twitch responses of single motor units in snake costocutaneous muscle have been recorded before and after conditioning tetanic stimulation. 2. Most units showed post-tetanic potentiation of twitch tension, associated with increased maximal rate of rise of twitch tension, and in some cases also associated with prolongation of twitch contraction time. A few units showed a short phase of actual depression of the post-tetanic twich responses, followed by potentiation. 3. The time course and magnitude of post-tetanic changes of twitch tension and maximal rate of rise of tension could be described by the sum of three processes which are assumed to be maximal close to the end of the conditioning tetanus: (i) a rapidly declining potentiation (called here early potentiation, which lasted less than 2 sec) which may have a purely mechanical origin; (ii) a much slower-declining potentiation (called here prolonged potentiation, which lasted up to 15 min); and (iii) a process which lasted up to 60 sec during which twitch potentiation was reduced. The latter process (called here depressed potentiation) was usually apparent as a marked trough in the plots of twitch amplitude versus time after the conditioning tetanus, and occassionally was evident as an actual transient depression of twitch amplitude after the tetanus compared with that before. 4. The effects of the prolonged potentiation and the depressed potentiation on the maximal effect of each process close to the end of the tetanus were extracted by fitting single exponential equations to different portions of the data, using a computer program. 5. Twitch potentiation associated with increased maximal rate of rise of tension seemed to be a separate phenomenon to that associated with prolongation of contraction time, seen when conditioning tetani of higher frequency and numbers of stimuli were employed. The depressed potentiation of twitch tension tended to be partly masked in cases where contraction time was prolonged, but this did not affect the depressed potentiation of maximal rate of rise of tension. 6. The post-tetanic potentiation shown by a unit was related to the contraction time of the unit, in addition to the well known relationship to the initial twitch-tetanus ratio. The depressed potentiation may correlat more closely with the initial twitch-tetanus ratio than with the unit contraction time. 7. The magnitude of maximal depressed potentiation shown by a unit may be directly correlated to that of maximal prolonged potentiation. 8. The time constant of decay for prolonged potentiation of twitch tension tended to be related inversely to unit contraction time and directly to unit size and the maximal value of prolonged potentiation oftwitch tension. The time constant of decay for prolonged potentiation of maximal rate of rise of tension tended to be related to unit size and initial twitch-tetanus ratio, and the time constant of decay for depressed potentiation of rate of rise of tension tended to be related to unit size. 9...

Properties of twitch motor units in snake costocutaneous muscle.

1. Single motor units of twitch muscle fibres were studied in isolated nerve-muscle preparations of m. costocutanei inferiores from grass and garter snakes. Preparations were superfused with Ringer solution at a controlled temperature of 22 degrees C.2. The peak and time-to-peak tension (contraction time) were measured for isometric twitches of forty-seven whole muscles and 83 motor units. The sample of motor units was drawn from an estimated total population of 213-355 twitch units. Peak tetanic tensions were also measured. The measurements were made at muscle lengths at which the twitch tension was maximal, and this length was not always the same for whole muscle and unit twitches. In fifty-nine cases 1 and in twelve cases 2 motor units were isolated from each muscle.3. Whole muscle contraction times ranged from 22-61 msec (mean +/- S.D. = 40.3 +/- 9.8 msec) and those for units from 18-92 msec (mean +/- S.D. = 46.9 +/- 15.9 msec). The wide range for whole muscles is discussed.4. The percentage of the whole muscle tetanic tension contributed by each unit (unit size) was calculated. Contraction time was inversely related to unit size.5. Twitch-tetanus ratios were calculated and found not to be related to unit contraction time.6. The conduction velocities of axons innervating 23 motor units were calculated from latency measurements at two points along the length of the nerve. They ranged from 1.9 to 10.4 m/sec. Axon conduction velocity was inversely related to unit contraction time, and directly related to unit size.

Mechanical properties of single motor units in the anterior belly of the digastric

Electromyograms were recorded from three subjects during steady, low-rate discharge of single motor units of anterior belly of digastric, accompanying maintenance of isometric tension. The overall tension developed in muscles subserving mandibular depression was recorded from a force transducer situated inferior to the mandibular symphysis. The force transducer output for the 100-msec period immediately following each of several hundred discharges of a single unit was averaged to obtain a characteristic tension curve for the contractile response (twitch) of that unit. Contraction times of units (time from initiation of tension increase to peak tension) ranged from 16 to 42 msec. Recorded peak twitch tensions ranged from 0.1 to 1.8 g. Consistent with the Size Principle [Henneman et al., J. Neurophys. 28 (1965)] which is based primarily on findings from animal and human skeletal muscle, and also with a study of human masseter and temporalis [Yemm, J. Physiol. 265 (1977)] later recruited (larger) units possessed higher twitch tensions. Contrary to the Size Principle, but in agreement with results from human masseter and temporalis, contraction times were not shorter in later recruited motor units.

The Relevance of the Correlation Between Tremor Frequency, Initial Firing Rate of Motoneurons and the Motor Unit's Contraction Time

A hypothesis about the origin of the physiological tremor on the basis of other hypotheses is presented. In order to find the muscle fiber candidates that produce the tremor. the muscle fibers and their motoneurons are classified into three groups: The silent fibers (1). the fibers that fire with their initial firing rate (2) and those firing with a high frequency (3). This classification is dynamical. A given muscle fiber can belong to anyone of the three groups. It depends on the threshold of the fiber and the actual excitation level of the motoneuron pool. to which group a fiber belongs. The group two fibers are responsible for, the genesis of the tremor. The reasons for this assumption are: 1. The twitches of the muscle fibers of group two are the least fused. 2. The motoneurons of this group have an augmented tendency to synchronisation. 3. The motor units of group two are the strongest (active) units. Therefore they are overrepresented in the total muscle force.