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Chemical energetics of single isometric tetani in mammalian smooth muscle.

A rabbit taenia coli preparation has been used to study the chemical energetics of smooth muscle contraction. Under the experimental conditions, the muscle had no spontaneous mechanical activity, but could be fully activated with the use of electrical field stimulation. ATP resynthesis from glycolysis and respiration was stopped with a procedure that involved treatment with metabolic inhibitors at 5 degrees C followed by rewarming to 18 degrees C. This procedure did not alter the high-energy phosphate contents of mechanical responses of the muscle. Use of this preparation to determine ATP and phosphorylcreatine changes during isometric tetani at 18 degrees C and a length of 86% LO showed that there was net ATP breakdown initially with no significant phosphorylcreatine splitting. This was followed by an increase in the rate of phosphorylcreatine splitting with net ATP synthesis. The average rate of total high-energy phosphate utilization was about 0.01 mumol/g.s for up to 60 s or about 150 times less than that of frog sartorius at the same temperature.

Adenosine Triphosphate↗

EMG analysis of lower limb muscles in humans during quick change in running directions.

Open and cross maneuvers for changing running direction were studied to characterize selective EMG activity between the maneuvers. Eleven subjects turned towards the right or the left during running. The gluteus medius modified foot trajectory of the leading leg during the open maneuver, whereas the sartorius worked modestly during the cross maneuver. Compared with the cross maneuver the open maneuver exhibited greater vastus medialis and gastrocnemius activity during the ground support phase, faster running speed and wider turning angle. These results suggest that the open maneuver is more effective than the cross maneuver for quickly changing running direction.

Adult↗

Synaptic strength as a function of motor unit size in the normal frog sartorius.

A wide range of motor unit sizes exists in each frog sartorius, with values of tetanus and twitch tensions extending over 62- and 400-fold ranges, respectively. These differences primarily represent differences in the number, rather than the size, of muscle fibres in each motor unit. Tetanus-to-twitch tension ratios varied markedly between different motor units, ranging from 1.5 to over 190. Because directly stimulated muscle fibres have tetanus/twitch ratios no larger than 3, it is concluded that high tetanus/twitch ratios arise from recruitment of muscle fibres during the tetanus which respond with only subthreshold depolarization during a twitch. Small motor units, as judged either by their twitch or tetanus tension, were associated with higher tetanus/twitch ratios, suggesting that the average safety margin of a motor unit increases with the motor unit's size. Indeed, when the tetanus/twitch ratio of a motor unit is used to determine the fraction of fibres in the unit with subthreshold neuromuscular junctions, it is observed that there is a direct linear relationship between the size of the motor unit and its over-all efficacy of synaptic transmission. Measurements of the effects of changes in calcium concentration on motor unit twitch tension confirmed the last conclusion. Furthermore, this analysis revealed that large motor units, although having a wide range of transmission safety margins, are largely comprised of junctions of uniformly high safety margin. In motor units of smaller size, synaptic strengths become more evenly distributed over a wide range of values. Small motor units had consistently longer twitch rise-times than did larger units. This decrease in rise-time with motor unit size paralleled the decrease in tetanus/twitch ratios, raising questions about the regulation of muscle fibre contraction kinetics.

Action Potentials↗

The sarcomere length--isometric tension diagram of the toad Bufo bufo sartorius.

The sarcomere length--isometric tension diagram has been determined for the toad Bufo bufo sartorius using a laser diffraction technique to measure the sarcomere width. The sarcomere width at l0 was found to be 2.37 micron. At length shorter than l0 this whole muscle exhibits a steeper decline in tension than single fibres. This discrepancy in the shape of the tension-length diagram between single frog fibres and whole toad sartorii may be due to a difference in the magnitude of the internal force which appears only at short lengths.

Animals↗

Postoperative evaluation of quadriceps contracture in children: comparison of three different procedures.

Sixty-five patients (73 legs) with quadriceps contracture involving mainly the rectus femoris muscle were operated on. The average follow-up was 6.3 years. In the postoperative overall results, the rating system score was significantly decreased from a preoperative mean of 7.0 points to a postoperative mean of 1.9 points. Three different operative methods were used: release of the pelvic origin, sartorius plasty and release of the pelvic origin, and sartorius plasty and release of the fibrosis. The most satisfactory results were obtained in the group treated by release of the fibrosis.

Adolescent↗

Mechanical activation in slow and twitch skeletal muscle fibres of the frog.

1. Slow and twitch muscle fibres of the frog were studied with a two-micro-electrode point voltage-clamp method. Slow fibres were identified in pyriformis and cruralis muscles by their appearance in the light microscope, electrical characteristics, and rate of sarcomere shortening or of tension development. 2. The relation between the amplitude and duration of threshold depolarizing pulses was determined in sartorius twitch and pyriformis slow fibres. Strength-duration relations for contractile activation are very similar in the two fibre types. 3. The effect of a brief subthreshold pulse on the threshold voltage level decays with a half-time of 1-2 msec at 9 degrees C in both slow and twitch fibres. This fast decay, thought to reflect voltage-dependent deactivation of Ca2+ release following repolarization, is followed by a slower decay of greatly different rates in the two fibre types. the slower components of decay might reflect the rate of background Ca2+ removal by the sarcoplasmic reticulum. 4. Reducing external Ca2+ levels to about about 0.1 microM with 2.5 mM-EGTA has no effect on the shapes of strength-duration curves for both slow and twitch fibres, suggesting that activator Ca2+ in both fibre types originates entirely from intracellular stores. 5. "Tonic' contractions were studied using voltage-clamped short cruralis slow fibres at 20 degrees C. Reducing external Ca2+ to about 0.1 microM had no effect on the steepness of the steady-state tension-voltage relation or on the ability of slow fibres to maintain maximal tension during long (200 sec) depolarizations to membrane potentials of up to +50 mV. 6. Functional similarities in activation kinetics of slow and twitch fibres are discussed in relation to the sensing of tubular membrane potential by the sarcoplasmic reticulum, to Ca2+ release from it, and to possible mechanisms involved in these processes. Processes leading to the rapid turning on and off of Ca2+ release in response to changes in tubular membrane potential are probably similar in slow and twitch fibres. However, the apparent lack of voltage-and time-dependent inactivation of Ca2+ release in slow fibre points to a major difference in the two types of muscle.

Animals↗

[Effect of hydrocortisone on neuromuscular transmission in the frog skeletal muscles].

Hydrocortisone (1.10(-7)-1.10(-5) M/l) in vitro experiments on frog's muscle in conditions of preliminary curarization increases dose-dependently the quantum content of e.p.p., affecting neither membrane potential, nor input resistance, nor sensitivity to acetylcholine of the membrane of m. sartorius fibers. Hydrocortisone in conditions of magnesium block of neuro-muscular transmission does not affect the evoked transmission. Hydrocortisone seems to facilitate the evoked quantum acetylcholine secretion only in the presence of curare and in conditions of initial high quantum content of e.p.p. The mechanism of hydrocortisone decurarization effect on neuro-muscular transmission is mainly of a presynaptic nature.

Acetylcholine↗

Modulation of ipsi- and contralateral reflex responses in unrestrained walking cats.

1. The modulation of reflex responses in up to 10 simultaneously recorded hindlimb muscles was studied in unrestrained cats walking on a treadmill. Single electrical shocks of various strengths were applied to different skin areas of teh hindlimb at different times of the step cycle while the resulting EMG responses were sampled and analyzed. 2. Two excitatory response peaks (P1 and P2) at a latency of about 10 and 25 ms, respectively, were seen in all flexors examined (sartorius, semitendinosus, tibialis anterior, extensor digitorum longus). Stimulation of most skin areas was effective but responses were most easily obtained from stimuli applied to the foot or ankle. During the step cycle there was a marked modulation of the amplitudes of the responses, especially the P2 responses, which grew larger toward the end of stance when a maximum was reached, followed by a steady decline throughout swing. This pattern was very similar for various flexors, although these muscles differed considerably in their normal EMG activity pattern during walking. 3. Flexor responses were absent when the same stimuli were applied during the early stance phase. Instead, inhibition of the ongoing EMG activity was seen at a latency of 10 ms or less in all extensors examined (semimembranosus, quadriceps, soleus, gastrocnemius medialis, flexor digitorum longus). The inhibition was followed by a late excitatory peak (P3) at about 35-ms latency in all extensors except soleus. 4. Certain stimulation sites yielded exceptions to the above patterns. Stimulation of the skin area innervated by the sural nerve yielded larger and earlier MG excitatory responses as compared to stimulation of other skin areas. Activation of the plantar surface of the foot often failed to elicit P2 responses in the hip flexor sartorius, which showed inhibition instead. 5. In the hindlimb contralateral to the stimulus, excitatory responses occurred both in flexors and extensors at a latency of 20-25 ms. The pattern of modulation of these responses was similar to the ipsilateral modulation of P2 flexor and P3 extensor responses. Soleus failed to show a crossed response. 6. The data indicate that flexor and extensor responses differ both with respect to their latency and to their correlation with the ongoing EMG reactivity. It is concluded that these stimuli do not demonstrate reflex reversal in the strict sense in the normal walking cat but that there is modulation of transmission in a flexor excitatory and extensor inhibitory pathway, possibly by the flexor part of the spinal locomotor oscillator. In addition, there are some specialized flexor inhibitory and extensor excitatory pathways. The slow soleus muscle does not seem to be excited through these pathways.

Animals↗

Effects of stimulation of hindlimb flexor group II afferents during fictive locomotion in the cat.

1. This study examines the effects of electrical stimulation of hindlimb flexor nerves on the fictive locomotion pattern. Locomotion was initiated by stimulation of the mesencephalic locomotor region in the decerebrate paralysed cat and monitored by recording the electroneurogram from selected hindlimb flexor and extensor muscle nerves. Flexor nerves were stimulated using short trains (20-50 stimuli at 100 Hz) during either the flexor or the extensor phase of the fictive locomotor cycle. 2. Stimulation of tibialis anterior (TA), posterior biceps and semitendinosus (PBSt) or sartorius (Sart) nerves at 5 times threshold (T) during the flexor phase of the fictive locomotor cycle terminated on-going activity in flexor nerves and initiated activity in extensors. Thus, flexor nerve stimulation during flexion shortened the locomotor cycle by resetting to extension. The failure of lower intensity (2T) stimulation of PBSt or Sart nerves to reset the step cycle to extension suggests that group II afferents are responsible for these actions. Resetting evoked by 2T stimulation of the TA nerve may be due to a high proportion of group II afferents with low electrical threshold. 3. During extension, stimulation of TA and PBSt nerves at 5T did not perturb the locomotor rhythm whereas Sart stimulation prolonged the locomotor cycle. 4. Stimulation of cutaneous or knee joint afferents failed to produce effects similar to those evoked by stimulation of flexor muscle nerves at group II strength. These findings are at odds with those obtained elsewhere in the acute spinal, DOPA fictive locomotion preparation. The possibility that group II resetting during fictive locomotion is not mediated by flexion reflex pathways but by previously unknown pathways released in the present preparation is discussed. 5. Since many of the flexor afferents recruited by 5T electrical stimulation are the length-sensitive group II fibres, spindle secondaries may act to regulate the duration and onset of flexor and extensor activity during real locomotion. The resetting from flexion to extension also suggests that unexpected or enhanced activity of flexor secondaries during swing would promote a switch of the step cycle to stance.

Animals↗

Temperature and synaptic efficacy in frog skeletal muscle.

1. Intracellular recording and voltage-clamp techniques were used to measure synaptic efficacy and the safety factor for neuromuscular transmission in frog skeletal muscle. All measurements were made in normal Ringer solution, in the absence of presynaptic or postsynaptic blocking agents. 2. Over a broad temperature range (10-30 degrees C), a small percentage of sartorius fibres (about 6%) could be found which produced only subthreshold end-plate potentials and no action potential in response to single, supramaximal nerve shock. At lower temperatures the proportion of such fibres increased; 42% of the fibres had subthreshold transmission at 5 degrees C, and 59% were subthreshold at 2.5 degrees C. 3. Threshold current, measured by intracellularly injecting short pulses of depolarizing current at end-plate regions, was independent of temperature between 2.5 and 20 degrees C. Thus, the reduced synaptic efficacy observed at low temperatures was not due to decreased electrical excitability of the postsynaptic membrane. 4. The amplitude of evoked end-plate currents (EPCs) decreased with cooling. At temperatures below 10 degrees C, the evoked EPCs at many end-plates were too small to initiate action potentials. The decline in EPC amplitude was due to three factors: a decrease in the amplitude of single quantum currents (MEPCs), an increase in the temporal dispersion of transmitter release, and (below 5 degrees C) a decrease in quantal content. 5. The safety factor for neuromuscular transmission decreased dramatically as temperature was lowered. At 30 degrees C average safety factor was large and positive (540 nA), but at 2.5 degrees C it was negative (-78 nA). 6. The quantal content of evoked transmitter release was independent of temperature change between 5 and 30 degrees C, the average value over this range being 180. However, at temperatures below 5 degrees C, quantal content fell off sharply (average value = 37). 7. The thermal independence of transmitter release may be an important mechanism in allowing poikilothermic animals to maintain physiological function over a wide range of body temperatures.

Action Potentials↗

Regulation of capillary blood flow and oxygen supply in skeletal muscle in dogs during hypoxaemia.

1. Multiwire surface electrodes were used to measure local hydrogen clearance curves and tissue PO2 in vivo. Evaluation of the initial slopes of the hydrogen clearance curves enabled the measurement of capillary blood flow and its distribution. 2. Capillary blood flow and tissue PO2 frequency distribution histograms were measured in the m. sartorius of anaesthetized, relaxed mongrel dogs under conditions of normoxic (Fi, O2 = 0.3) and hypoxic (Fi, O2 = 0.15 and 0.1) artificial ventilation. 3. Stepwise hypoxaemia (hypoxic hypoxia) induced an increasing discrepancy between capillary blood flow and arterial blood flow. The former decreased by 6% whereas the latter increased by 86%. 4. PO2 histograms provided no evidence of cellular anoxia even at Fi,O2 = 0.1. Capillary blood flow histograms suggested a redistribution of the local pattern of flow. 5. A 34.7% reduction of O2 consumption was observed as the result of severe hypoxaemia. 6. The concept of heterogeneity of capillary blood flow as a functional O2 reserve is presented, together with evidence for oxygen-dependent regulation of capillary blood flow and oxygen consumption.

Animals↗