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M Kuno

Publications and source records attributed to M Kuno.

At least 127 records · Page 7Linked to original sources

Electrophysiological properties of spinal motoneurones of normal and dystrophic mice.

1. The properties of spinal motoneurones of normal and dystrophic mice (129/ReJ) were examined with intracellular electrodes. 2. The following parameters of spinal motoneurones showed no significant differences between normal and dystrophic mice: resting and action potentials, the amplitude and duration of after-hyperpolarization, rheobasic current for excitation, threshold for excitation of the somadendritic membrane (IS-SD inflexion) and input resistance. 3. The changes in motoneurone properties observed 13-16 days after section of the sciatic nerve (axotomy) were similar in both normal and dystrophic mice. 4. The axonal conduction velocity of motoneurones in dystrophic mice was about ten times slower than that in normal mice. The conduction velocity of the sciatic nerve was only about 25% slower in dystrophic mice than in the normal animal. The estimated ventral root conduction velocity as well as the observed dorsal root conduction velocity in dystrophic mice was at least twenty times slower than that in normal mice. 5. In dystrophic mice, spinal motoneurones often showed multiple discharges in response to single, antidromic stimuli. The site of initiation of multiple discharge was located in the motor axon rather than in the motoneurone cell body. 6. In dystrophic mice, nerve impulses were transmitted from fibre to fibre ('cross-talk'). The site of impulse transmission among nerve fibres was near the distal portion of the spinal roots. 7. Synaptic potentials and peripheral reflex discharges evoked by stimulation of the dorsal roots showed a longer latency and were more prolonged in dystrophic mice than in the control mice. 8. The motoneurone properties of dystrophic mice showed no tendency of progressive changes with age ranging from 63 to 148 days. 9. It is concluded that the properties of motoneurone cell bodies examined in dystrophic mice are indistinguishable from those in normal mice and that the only abnormality in motoneurones of the former residues in the motor axon. 10. It is suggested that integrity of the discharge pattern of spinal motoneurones in dystrophic mice is interfered by anomalous impluse transmission in the motor axons and that the motoneurones in dystrophic mice are a homogeneous group rather than a mixture of "normal" and "abnormal" neurones.

Action Potentials↗

Differentiation of motoneurones and skeletal muscles in kittens.

1. Isometric contractions of the medial gastrocnemius (fast switch) and soleus (slow twitch) muscles were recorded in kittens ranging in age from 3 to 112 days, as well as in adult cats. 2. It was confirmed that the speed of contraction of the gastrocnemius muscle becomes progressively faster during the first few weeks after birth, whereas contraction times of the soleus muscle show little changes or a slight prolongation during the period of post-natal development. 3. The properties of gastrocnemius (fast alpha) and soleus (slow alpha) motoneurons were examined with intracellular electrodes in kittens at three different stages; 16-20, 61-71 and 100-112 days in age. 4. The axonal conduction velocities of both gastrocnemius and soleus motoneurones increased monotonically throughout the period of development and showed no correlation with post-natal changes in contraction times of the innervated muscles. 5. The duration of after-hyperpolarization in soleus motoneurones became progressively longer with age, while that in gastrocnemius motoneurones remained virtually unchanged during development. 6. The relation between the duration of after-hyperpolarization and the axonal conduction velocity in kitten motoneurones was similar to that observed in axotomized motoneurones of adult cats. 7. It is suggested that fast and slow alpha motoneurones show postnatal differentiation in terms of the duration of after-hyperpolarization and that axotomy leads to 'dedifferentiation' of the motoneurone properties. 8. Post-natal changes in the contractile properties of skeletal muscles were independent of the changes in the duration of after-hyperpolarization of the innervating motoneurones. However, it remains uncertain whether muscle differentiation is independent of the discharge pattern of the innervating motoneurones.

Age Factors↗

Differential reaction of fast and slow alpha-motoneurones to axotomy.

1. The properties of medial gastrocnemius (m.g., fast alpha) and soleus (sol., slow alpha) motoneurones of the cat were examined with intracellular electrodes 8-119 days after section of the muscle nerves.2. The axonal conduction velocity was significantly decreased in both m.g. and sol. motoneurones after chronic section of the muscle nerves.3. The amplitude of overshoot of action potentials was significantly increased in both m.g. and sol. motoneurones following section of the muscle nerves.4. No significant changes in the resting membrane potential or the input resistance were observed for sol. motoneurones, whereas m.g. motoneurones showed a slight decrease in the resting potential and a slight increase in the input resistance.5. The duration of after-hyperpolarization was significantly decreased in sol. motoneurones, whereas that in m.g. motoneurones remained virtually unchanged or increased slightly following section of the muscle nerves.6. The changes described above were not seen in the preparations examined 29-46 days after section of the lumbosacral dorsal roots, suggesting that alterations in the motoneurone properties observed after section of the muscle nerves resulted from axotomy of the motoneurones rather than from sensory deprivation.7. The differences in electrophysiological properties between m.g. and sol. motoneurones were less prominent in axotomized animals than in control, unoperated cats.8. It is concluded that fast (m.g.) and slow (sol.) alpha-motoneurones have qualitatively different properties. A possible ;dedifferentiation' of fast and slow alpha-motoneurones by axotomy is discussed.

Action Potentials↗

Properties of fast and slow alpha motoneurones following motor reinnervation.

1. The properties of medial gastrocnemius (fast alpha) and soleus (slow alpha) motoneurones of the cat were examined with intracellular electrodes 33-154 days after self- or cross-union of the muscle nerves.2. The original properties of fast and slow alpha motoneurones measured in terms of the axonal conduction velocity, the duration of after-hyperpolarization and the overshoot amplitude were restored at least in part after self-union of the muscle nerves.3. Slow alpha motoneurones recovered their original properties whether the muscle nerve was united to the original, slow red muscle or to the fast pale muscle. In two animals, some of the fast muscle fibres seemed to be doubly innervated by both fast and slow alpha motoneurones.4. The degree of restoration of the original motoneurone properties was closely related to the degree of motor reinnervation of the muscle.5. At a given stage of motor reinnervation, the degree of recovery of the motoneurone properties was approximately the same regardless of the presence or absence of functional motor connexions of the motoneurone under study.6. When the dorsal root ganglia were removed immediately before self-union of the muscle nerves, recovery of the conduction velocity of motoneurones was impeded without significant effect upon the process of motor reinnervation or upon recovery of the overshoot amplitude and the duration of after-hyperpolarization.7. It is concluded that the ;dedifferentiated' properties of fast and slow alpha motoneurones after nerve section may be ;redifferentiated' following motor reinnervation to any muscle. The possible signal for restoration of the motoneurone properties is discussed.

Action Potentials↗

Sensory inputs to neurones in Clarke's column from muscle, cutaneous and joint receptors.

1. Discharge of neurones at the region of Clarke's column of the cat was recorded intracellularly or extracellularly in response to electrical stimulation of various hind limb nerves or to adequate stimuli applied to a variety of sensory receptors.2. According to the type of excitatory sensory input, the neurones were classified into four groups. Their relative proportions were: muscle group, 55-65%; cutaneous group, 15-25%; joint group, 5-15%; convergent group, 10-20%.3. The location of the neurone cell bodies was examined by marking the site of extracellular recording with fast green. The neurones of the muscle or cutaneous group were found to be within Clarke's column. One out of four neurones tested for the joint group and two out of six cells examined for the convergent group were found to be located outside the column.4. There was no difference in axonal conduction velocity among the neurones of different groups.5. The neurones of different groups could be distinguished in terms of the pattern of discharges recorded under ;resting' conditions and during activation of sensory receptors. It is suggested that information carried by dorsal spinocerebellar tract neurones to the cerebellum has a lower signal-to-noise ratio for cutaneous inputs than for muscle or joint inputs.

Animals↗

Synaptic action on Clarke's column neurones in relation to afferent terminal size.

1. Excitatory post-synaptic potentials (e.p.s.p.s) were recorded intracellularly from Clarke's column neurones (DSCT neurones) of the cat in response to adequate stimuli applied to a variety of sensory receptors.2. The amplitude of e.p.s.p.s so produced varied from less than 0.2 mV to more than 2-3 mV. The amplitude distribution of e.p.s.p.s suggested that the mean number of ;quanta' of transmitter released by one impulse varied widely from one fibre to another arising from a given type of sensory receptor.3. The average amplitude of e.p.s.p.s evoked by single afferent impulses was significantly smaller for cutaneous inputs than for muscle or joint inputs. However, synaptic action on DSCT neurones produced by different sensory inputs was equally greater, on the average, than that on spinal motoneurones.4. Both small and large e.p.s.p.s in DSCT neurones failed to increase in amplitude during post-synaptic hyperpolarization applied through the cell body. This failure could not be attributed to possible anomalous rectification in the post-synaptic membrane.5. Small and large e.p.s.p.s were comparable in half-decay time, but there was a positive correlation between amplitude and time-to-peak of e.p.s.p.s. It is suggested that the locations of synapses responsible for small and large e.p.s.p.s are intermingled on the dendrites and that large e.p.s.p.s are associated with a longer duration of transmitter action than small e.p.s.p.s.6. Degenerating terminals of primary afferent fibres on DSCT neurones and motoneurones were examined with the electron microscope after chronic section of the dorsal roots.7. Dendritic degenerating terminals showed no significant difference in size between motoneurones and DSCT neurones. Degenerating ;giant' terminals were found on DSCT neurones, but they were located only on or very close to the cell body.8. It is concluded that the major factor responsible for a large number of ;quanta' of transmitter released at synapses on DSCT neurones is the number of multiple synaptic contacts formed by one afferent fibre rather than the size of individual synapses.

Animals↗

Facilitation of monosynaptic excitatory synaptic potentials in spinal motoneurones evoked by internuncial impulses.

1. Descending tracts and primary afferent fibres were chronically degenerated in the lumbosacral cord of the cat, and attempts were made to evoke monosynaptic e.p.s.p.s in motoneurones by stimulation of interneurones with a pair of fine electrodes inserted into the cord.2. The reversal potential of monosynaptic e.p.s.p.s so produced was more negative than that measured for monosynaptic e.p.s.p.s produced by afferent impulses.3. Monosynaptic e.p.s.p.s evoked in motoneurones by internuncial impulses showed a significantly greater facilitation than those produced by afferent impulses.4. Monosynaptic e.p.s.p.s in a motoneurone produced by supramaximal intraspinal stimuli often revealed a fluctuation in amplitude. In such cases, when two successive stimuli were applied at a short interval, the mean amplitude of the second e.p.s.p.s was greater than that of the first e.p.s.p.s. This facilitation was associated with a decrease in the coefficient of variation of the e.p.s.p. amplitude fluctuation.5. The degree of facilitation of monosynaptic e.p.s.p.s evoked by internuncial impulses was not related to the amount of transmitter released by the preceding impulses.6. It is concluded that facilitation of monosynaptic e.p.s.p.s evoked by both afferent and internuncial impulses is based on the same mechanism and that the degree of facilitation of e.p.s.p.s is entirely determined by the nature of presynaptic elements.

Animals↗

Quantal components of the inhibitory synaptic potential in spinal mononeurones of the cat.

1. Monosynaptic i.p.s.p.s were produced in spinal motoneurones of the cat by stimulation of a pool of interneurones following chronic degeneration of descending tracts and primary afferent fibres in the lumbosacral cord.2. Monosynaptic i.p.s.p.s so evoked by supramaximal stimuli often showed a fluctuation in amplitude with occasional failures of response.3. When two successive stimuli were applied at a short interval, the mean amplitude of the second i.p.s.p.s was greater than that of the first. This facilitation was associated with a decrease in the number of failures, a decrease in the coefficient of variation of the amplitude distribution and an increase in the probability of occurrences of large i.p.s.p.s.4. A statistical analysis of the i.p.s.p. amplitude fluctuation showed that the monosynaptic i.p.s.p. is composed of discrete unit potentials evoked with a certain probability in a manner described by a binomial law.5. The application of strychnine decreased the mean amplitude of i.p.s.p.s with little change in the coefficient of variation of the i.p.s.p. amplitude distribution.6. It is concluded that the release of inhibitory transmitter occurs in quantal steps and that strychnine blocks primarily the post-synaptic receptors for the inhibitory transmitter.

Animals↗

Correlation between nerve terminal size and transmitter release at the neuromuscular junction of the frog.

1. End-plate potentials were recorded intracellularly at the frog neuromuscular junction bathed in a solution containing a low concentration of calcium and a high concentration of magnesium.2. The muscle was subsequently subjected to ;cholinesterase staining', and the area of the individual end-plates, studied with intracellular electrodes, was measured.3. A positive correlation was found between the end-plate area and the diameter of muscle fibres.4. The mean quantum content (m) showed a positive correlation with the size of end-plates.5. The frequency of spontaneous miniature end-plate potentials was positively correlated with m as well as with end-plate area.6. It is concluded that the amount of transmitter released following nerve stimulation is related to the size of nerve endings.

Animals↗

Enhancement of synaptic transmission by dendritic potentials in chromatolysed motoneurones of the cat.

1. Monosynaptic transmission in cat lumbosacral motoneurones undergoing chromatolysis was studied by intracellular recording from 7 to 20 days after section of the appropriate ventral roots.2. The average input resistance measured by passing polarizing currents across the cell membrane showed no significant difference between normal and chromatolysed motoneurones. Average rheobasic current for chromatolysed motoneurones was significantly lower (by about 30%) than that for normal motoneurones.3. Spike-like partial responses were commonly superimposed on monosynaptic EPSPs in chromatolysed motoneurones. These responses could be eliminated by stimulation of the bulbar inhibitory reticular formation, but could not be blocked by hyperpolarization applied to the motoneurone soma.4. The spike-like partial response in chromatolysed motoneurones showed a refractory period following (i) the antidromic invasion of the neurone generated by ventral root stimulation, and (ii) in response to two successive afferent stimuli. The refractory period ranged from 5 to 13 msec.5. Initiation of the partial response had no direct relation with the amplitude of the underlying EPSP. The partial response could be evoked by small EPSPs of about 0.5 mV.6. The action potential of a chromatolysed motoneurone arose from the partial response at different levels of depolarization, showing multiple trigger zones for spike initiation. Occasionally, chromatolysed motoneurones discharged in response to stimulation of a single afferent fibre.7. In neurones where more than one spike-like response was obtained, interaction between dendritic responses showed no refractoriness.8. It is concluded that the partial response is an all-or-none event originating at some discrete site on dendrites, and that its presence increases the efficacy of synaptic excitation in chromatolysed motoneurones.

Action Potentials↗

Alterations of synaptic action in chromatolysed motoneurones of the cat.

1. Monosynaptic EPSPs in lumbosacral motoneurones undergoing chromatolysis were studied by intracellular recording from 7 to 20 days after section of the appropriate ventral roots of the cat.2. The maximum monosynaptic EPSPs evoked in chromatolysed motoneurones by afferent volleys from the biceps-semitendinosus or the triceps surae muscles ranged from 1.0 to 9.5 mV in amplitude. The time-to-peak of these EPSPs was 1.7 msec on the average. These values were significantly smaller and longer, respectively, than the amplitude and the time-to-peak of monosynaptic EPSPs observed in normal motoneurones. The long time-to-peak of EPSPs in chromatolysed motoneurones could not be accounted for by asynchronous transmitter release.3. The mean number of unit EPSPs responding to a single afferent impulse (m) in chromatolysed motoneurones was comparable to that found in normal motoneurones.4. The amplitude of unit EPSPs estimated from the mean EPSP amplitude and the m value following stimulation of a single afferent fibre was significantly smaller in chromatolysed motoneurones than in normal motoneurones. This difference was attributed to a difference in synaptic location.5. The shape of monosynaptic EPSPs evoked in chromatolysed motoneurones by stimulation of single afferent fibres was analysed on the basis of Rall's compartment model. The analysis suggested that there is a lack of the excitatory synaptic input to the cell body in chromatolysed motoneurones.6. Similar alterations were also found in IPSPs. The degree of change in synaptic responses evoked by stimulation of various pathways appears to depend on the synaptic location.7. Following the study of the interaction of several inputs on the motoneurone and of their dependence on membrane potential, a tentative model of the synaptic distribution of different pathways is proposed.

Animals↗

Post-tetanic hyperpolarization produced by an electrogenic pump in dorsal spinocerebellar tract neurones of the cat.

1. Hyperpolarization following single and repetitive excitation of dorsal spinocerebellar tract (DSCT) neurones of the cat was studied by intracellular recording.2. Hyperpolarization following an antidromic action potential consisted of an initial, brief phase (undershoot) and a late, prolonged phase. The latter hyperpolarization was independent of the membrane potential, whereas the former was reversed in polarity by hyperpolarizing pulses applied across the DSCT cell membrane.3. DSCT neurones showed a prolonged hyperpolarization after a train of antidromic action potentials. The amplitude and duration of the hyperpolarization were dependent on the number and the frequency of action potentials. A similar hyperpolarization was observed following a train of impulses evoked by depolarizing pulses applied through the intracellular electrode.4. There was no detectable conductance change during the post-tetanic hyperpolarization. The latter showed no reversal potential when the membrane potential was altered.5. The half-decay time of the post-tetanic hyperpolarization was lengthened when the cord temperature was lowered. The temperature coefficient (Q(10)) was 2.4 within the range of 31-40 degrees C.6. The amplitude of the undershoot following each action potential was assumed to provide a criterion for the accumulation of the extracellular K(+). Alterations in the amplitude of undershoots during repetitive excitation suggested that the duration of post-tetanic hyperpolarization depends on the accumulation of extracellular K(+) as well as of intracellular Na(+) associated with a train of impulses.7. It is suggested that post-tetanic hyperpolarization is produced by an electrogenic sodium pump. A possible significance of such a hyperpolarization in impulse coding is discussed.

Action Potentials↗

Non-linear summation of unit synaptic potentials in spinal motoneurones of the cat.

1. Monosynaptic excitatory post-synaptic potentials (EPSPs) produced in spinal motoneurones of the cat by stimulation of a single afferent fibre were recorded with intracellular electrodes.2. In total, seventy-three triceps surae motoneurones were studied with stimulation of thirty-six different afferent fibres.3. The mean amplitude of the EPSPs evoked by single afferent impulses ranged from 0.06 to 2.0 mV with an average of 0.27 mV.4. The mean number of unit EPSPs responding to a single afferent impulse (m) was calculated from the number of failures. The values ranged from 0.7 to more than 5. About 10% of the sample showed no failure of synaptic response in about 200 consecutive trials. The m values for these synaptic responses were estimated to range from 5 to 15.5. In the majority of tests, the observed amplitude fluctuations of monosynaptic EPSPs evoked by stimulation of a single fibre were less than those expected from Poisson's law. This discrepancy may be accounted for by non-linear summation of the unit EPSPs at dendritic synaptic sites.6. It is suggested that the synaptic responses initiated at different sites of a motoneurone may summate linearly at the soma, although summation of unit EPSPs is non-linear at individual synaptic sites.

Animals↗

Analysis of synaptic efficacy in spinal motoneurones from 'quantum' aspects.

1. Synaptic responses of triceps surae motoneurones of the cat following stimulation of single afferent fibres were examined by intracellular recording techniques.2. The mean quantum content (m) of monosynaptic excitatory postsynaptic potentials (EPSPs) was independent of the type of motoneurone recorded and of the afferent fibre stimulated. There was no significant difference in m value between homonymous and heteronymous synapses.3. A positive correlation was found between the amplitude of unit EPSPs and the input resistance of motoneurones. The difference in the amplitude of unit EPSPs appears to be responsible for the higher synaptic efficacy in slow-conducting motoneurones than in fast-conducting motoneurones.4. There was no significant difference in the time course of monosynaptic EPSPs evoked by impulses from homonymous and heteronymous afferent fibres.5. The ratio of monosynaptic connexions from a given afferent fibre was significantly greater on to homonymous than to heteronymous motoneurones. It is concluded that the difference in efficacy between homonymous and heteronymous synaptic transmission is due to the difference in the number of afferent fibres converging upon these motoneurones.

Animals↗