Motor unit recruitment order in neuropathic disease.
Explore the source record for details and available documents.
Biomedical subjects
Publications and source records attributed to K Reiners.
Explore the source record for details and available documents.
During recording of physiological postural hand tremor over a period of 60 min tremor peak frequency (PF) did not change in 14 normal subjects as long as the mechanical conditions were not changed. In contrast, tremor amplitude and synchronization of the corresponding EMG varied considerably. Any alteration in hand mechanics such as changing hand position or adding masses led to changes of PF according to the alteration in mechanical resonant properties. The results show that PF of physiological postural hand tremor is mainly determined by mechanical factors. There is no evidence for a systematic decrease of PF (Stiles et al. 1976) or for the emergence of a formerly described (Lippold 1981) 4-6 Hz tremor component with prolonged maintenance of posture. In the pathological tremor forms of Parkinson's disease or essential tremor PF also remained unchanged during prolonged maintenance of posture.
In order to test the regenerative capacity of atrophic axons, a constricting ligature was placed around the proximal tibial nerve of the rabbit, and the nerve crushed at the ankle one week later. Axonal atrophy with altered g ratios was subsequently confirmed in fibres distal to the site of ligature and proximal to the site of crush. In nerves with tight proximal ligatures the reinnervation of plantar muscles and the subsequent recovery of distal motor latency were delayed, indicating impaired regeneration. This result may be relevant to the "double-crush" theory of nerve damage.
The effect of changes in mechanical limb properties on the peak frequency of different tremor forms was analysed. Wrist tremor was recorded by an accelerometer fixed to the dorsum of the hand and demodulated surface EMG was recorded from the wrist extensors, while the extended hand was loaded with successively heavier weights. Physiological tremor was characterised by flat EMG spectra and a gradual decrease in tremor peak frequency with increasing load, as would be expected from the properties of a passive spring-mass-system. Also the peak frequency of activated physiological tremor characterised by increased synchronisation between motor units decreased in frequency with increasing loads. EMG spectra showed clear peaks of activity at the various mechanically determined tremor frequencies. In contrast, in two pathological tremor forms, the postural tremor in Parkinsonian patients and essential tremor, peak frequency tended to remain stable irrespective of changes in load. The method therefore allows a simple distinction between physiological and these two pathological tremors.
Rabbits were immunized with galactocerebroside and a crush lesion was created in the tibial nerve before the onset of experimental allergic neuritis. Normal regeneration and myelination of distal peripheral nerve sprouts occurred and was identical to that of controls, although circulating antigalactocerebroside antibodies were present and nerve roots showed typical signs of beginning experimental allergic neuritis.
Starting from the observation that the part above 6 Hz of the power spectrum of force tremor during isometric contractions can be related to the unfused twitches of motor units firing asynchronously, an attempt was made to study the usefulness of force tremor spectral analysis as a global descriptor of motoneurone pool activity. To compensate for the mechanical low-pass filter characteristic of skeletal muscle which leads to increased damping of mechanical ripples at higher frequencies, a numerical compensation rule was derived from data obtained by electrical microstimulation of small ensembles of motor units (MUs). Hidden line plots of consecutive partially overlapping spectra allowed visualization of changes in spectral composition during ongoing muscle activity. The resulting muscle activity spectra (MAS) showed broad peaks according to the range of onset firing rates in normal subjects. These tended to shift to higher frequencies with increasing force. Under conditions with increased synchronization of the MUs these broad peaks were replaced by sharp peaks corresponding to the burst repetition rate. Patients with different motor dysfunctions were selected to illustrate how alterations of MU activity are reflected in the MAS. Decreased or increased firing rates were observed as well as abnormal states of synchronization. It is concluded that the MAS provides useful information about some aspects of the discharge characteristics of ensembles of MUs and therefore represents a method to monitor some qualitative 'image' of the MU activities within a muscle.
The relationship between the action potential amplitude and the threshold force of recruitment of 275 motor units (MU) recorded from the first dorsal interosseus muscle of 15 healthy subjects was analysed. The number of newly recruited MU decreased exponentially with increasing muscular force. Action potential amplitudes showed a highly significant positive linear correlation with threshold force of recruitment. This relationship is in accordance with the size principle of MU recruitment. Applying the rank correlation method, 88.6 +/- 2.0% (mean +/- standard deviation) of paired comparisons between all MU of one subject followed the normal activation sequence of MU with an increasing action potential amplitude. It is shown that small variations of the distance between the leading-off surface of the electrode and the MU recorded do not affect these findings. These results demonstrate that the force at which a MU is recruited is the most important factor influencing MU action potential amplitude in normal subjects. So far this fact has not been adequately appreciated in clinical electromyography although it is of significance for the assessment of pathological conditions.
In 23 guinea-pigs a constricting ligature was placed on the tibial nerve in the thigh on one side, in order to produce axonal atrophy in the distal part of the nerve. Either before or after ligature, 10 of the guinea-pigs received subcutaneous diphtheria toxin into the abdominal wall, in a dose insufficient to cause generalised paralysis or reduced motor conduction velocity (MCV). In 7 of the 10 animals, MCV distal to the ligature fell below the range seen after ligature alone. In animals which had received toxin histological studies revealed paranodal and segmental demyelination in the distal tibial nerve, which was more extensive on the side of the ligature than in the opposite leg. Occasional paranodal but no segmental demyelination was seen distal to ligature alone. These results indicate that a small dose of systemic diphtheria toxin is more likely to produce peripheral nerve demyelination if an axonal abnormality is also present.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
An enzymatic method is described for isolating intact parenchymal cells from rat livers. 3--4 g cells (wet weight) could be isolated from livers of rats weighing 180--230 g. After an in vitro preperfusion of 15 minutes with a Ca-free buffer, collagenase (200 mg/1) and calcium chloride (5.2 mmol/1) were added. Perfusion was continued for another 15 minutes at 37 degrees C. Micromorphological integrity of cell membranes was demonstrated by scanning electron microscopy. With regard to rates of gluconeogenesis and protein synthesis, parenchymal cells isolated according to our method were found to be superior to liver slices and cells isolated by other methods. Ratios of ATP/ADP (5.69) and of lactate/pyruvate (8.64) as parameters of the energetic situation and the redox state resp. were found within the physiological range. Integrity of cell surface receptors was proved by their sensitivity to epinephrine, glucagon and insulin. Glucagon (0.3 mumol/1) and epinephrine (1 mumol/1) and reduced glycogen deposition in hepatocytes of fasted rats by 84.9 % and 95.9 % resp. Both hormones stimulated glycogenolysis in parenchymal cells of fed rats to a similar extent. Urea synthesis was stimulated 29.5 % by glucagon (1 mumol/1), and inhibited 28.0 % by insulin (10 nmol/1). The stimulatory effect of glucagon (1 mumol/1) was abolished by insulin (10 nmol/1).
Chronic progressive of relapsing inflammatory polyneuropathy (CRIP) can be treated effectively with immunosuppressive drugs and/or plasma exchange (PE). This report describes a patient who responded dramatically and reproducibly to PE during four successive relapses and remained in remission while on medical immunosuppression with azathioprine and corticosteroids. The clinical course was closely correlated with electrophysiologic parameters such as compound muscle action potential amplitudes and distal latencies. The purified IgG fraction of PE filtrate bound to rat and human sciatic nerve on immunohistochemistry. Furthermore, a similar staining pattern was achieved by purified Fab fragments, which was absent in all control preparations. These findings support the hypothesis that circulating plasma factors may play a role in CRIP and that one of these factors may be an IgG antibody to peripheral nerve components.
In situ studies on muscle fiber conduction velocity (MFCV) were performed in 54 patients with histologically and biochemically defined myopathies. MFCV was measured over a 10 cm segment of the rectus femoris muscle by intramuscular stimulation and recording. Muscle disorders included muscular dystrophies, myotonic dystrophy, inflammatory myopathies, metabolic myopathies, endocrine myopathies, and congenital myopathies with structural abnormalities. Ten healthy volunteers served as controls. MFCV was significantly reduced in all patients except those with a defect in glycolysis and those that had recovered from acute myositis. MFCV did not vary with either sex. age or the duration of the disease. This shows that MFCV slowing is an unspecific finding in most myopathies. However, in some patients with normal needle electromyography, MFCV provided additional information in diagnosing muscle disease.
A simple method is described for the rapid assessment of respiratory heart-rate variation (HRV) by making use of an EMG machine to record the RR-interval of the electrocardiogram. The built-in software for single-fibre EMG usually incorporated in modern EMG equipment is sufficient for a rapid data analysis based on the difference between the shortest and longest RR-intervals recorded over a period of 60 to 100 s. Measurements of HRV obtained by our new method correlate well with those obtained by the more tedious conventional manual measurement of an ECG recording (r = 0.88).