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Various models of chronic muscular activity, as workload training, tendon transfer, or paresis and peripheral nerve damage are examples leading to muscle overload, which may induce measurable effects in motor units. The aim of this study was to investigate whether 5-week overloading of muscles connected with their voluntary activation in a running wheel and by a treadmill training change electrophysiological properties of their motoneurons. Rats were subjected to chronic overload of the medial gastrocnemius (MG) muscle by cutting the lateral gastrocnemius, soleus and plantaris muscles from the Achilles tendon and sewing them directed proximally to the skin. As the result of this operation, only the MG muscle was able to evoke a foot plantar flexion during the daily locomotor activity. After one week of convalescence, rats were subjected to extensive voluntary activity on a running wheel and additionally to a training program on a treadmill (1 hour daily with a speed of 27 cm/s) for 5 weeks, 5 days a week. The acute experiments were carried out on the MG motoneurones in deeply anaesthetized animals. Intracellular recordings were performed from MG motoneurones located in L4-L5 spinal segments using glass micropipettes filled with 2 M potassium citrate solution. The results were compared to the control group of normally active, intact animals. Parameters of antidromic action potentials were measured and effects of intracellular injection of rectangular pulses of depolarization current were analyzed. The basic electrophysiological properties were considerably modified by the overloading either in fast and slow motoneurones. Moreover, we observed changes in their rhythmic properties, as the increased maximum steady-state frequencies of motoneuronal firing resulting in changes in the course of the steady-state frequency-current curves in the overloaded animals. The results of this study may help understand neuromuscular mechanisms of plasticity of overloaded muscles.
Plasticity of motor unit (MU) contractile properties observed as a result of various forms of altered physical activity or neurological disorders often leads to difficulties in their division into fast and slow types on a basis of standard physiological criteria (sag disappearance, changes of the contraction time). A method to recognize fast or slow MU types on a basis of a profile of tetanic contraction evoked at 20 Hz frequency has been proposed. We evaluated its efficiency in the male and female rats, after several types of a physical training (locomotor training, whole-body-vibration), and after various spinal cord injuries (transection or hemisection). Analogical method was used to distinguish fast and slow MUs in the cat muscle. Functionally isolated MUs of the medial gastrocnemious muscle were investigated, and the 20 Hz Tetanus Index was calculated for each MU as a ratio of the peak force in a response to the last stimulus within the unfused 20 Hz tetanus to the peak force following the first stimulus. For fast MUs values of this index were lower than 2.0, and for slow MUs higher than 2.0 in either group investigated. However in the cat muscle, composed of MUs with considerably longer twitch-time characteristics, the stimulation frequency, which enabled us to receive comparable results was lower (15 Hz) and border value of the index amounted to 5.0.
The whole body vibration training was performed on adult male Wistar rats. The experimental group subjected to a whole body vibration consisted of seven rats, while the control group of nine rats. The training program included 5 weeks and was applied by 5 days a week. Each daily session consisted of four 30-s runs of vibration at 50 Hz. Intracellular properties of motoneurones were investigated during experiments on deeply anesthetized animals. It was demonstrated that a whole body vibration evoked adaptations in excitability and firing properties of fast-type motoneurons, exclusively. A significant decrease in rheobase current and a decrease in the minimum and the maximum currents required to evoke steady-state firing in motoneurons were revealed. These changes resulted in a leftward shift of the frequency-current relationship, combined with an increase in slope of this curve. These results showed that fast motoneurons of rats after vibration have the ability to produce series of action potentials at higher frequencies in a response to the same intensity of activation. Obtained data provided direct evidence on motoneuronal plasticity following a whole body vibration.
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