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Results for “Motor Neurons, Gamma”

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At least 19 recordsLinked to original sources
PubMed1975

[Disorder of gamma-motor neuronal activity in experimental thyrotoxicosis].

The activity of gamma-motor neurons was studied in the anesthetized rats following per os administration of thyroidin for 3 weeks. In experimental thyrotoxicosis against the backgrounds of an increased amount of mute filaments isolated from the stem of the n. gastrocnemius there was an increase in the frequency of discharge of the flexors and extensors of the gamma-motor neurons. A high frequency not peculiar to that of intact animals was recorded in the flexors of the gamma-motor neurons of the animals receiving thyroidin.

Animals↗
PubMed1982

Quantitative analyses of neuronal development in the lateral motor column of mouse spinal cord. III. Generation and settling patterns of large and small neurons.

The generation and settling patterns of large and small lateral motor column (LMC) neurons were compared in the spinal cords of three inbred strains of mice by means of tritiated thymidine autoradiography. No significant strain differences were observed for the number of large LMC cells (presumptive alpha motor neurons) that were heavily labeled on each injection day, although there were significant strain variations for this measure with regard to small LMC neurons (presumed gamma motor neurons and interneurons). The generation of both large and small LMC neurons began at the same time, but peak production of large cells preceded that of the small neurons. There were no strain differences observed for this relationship between the large and small cells. These findings indicate that the LMC, from the time of its initial formation, contains cells destined to become large and small neurons. The positions of large and small neurons within the adult LMC relative to their times of origin (settling patterns) were analyzed statistically. A significant ventrodorsal sequence for early-to-late generated cells was observed for both large and small LMC neurons. No significant strain differences were found in the analysis of settling patterns. A ventrodorsal settling pattern also has been described for amphibia (Prestige, '73) and, in conjunction with the proximodistal sequence of limb development described by other investigators, the ventrodorsal sequence could play a key role in the development of motor neuronal somatotopic organization.

Animals↗
PubMed1996

Estimation of certain parameters of a stationary hybrid process involving a time series and a point process.

A method is presented for estimating the cross-spectral density of a hybrid process involving a time series and a point process. The method is based on the generalized cross-periodogram statistic, which is smoothed by splitting the whole record of the data into a number of disjoint subrecords. Estimates of the coherence function and the cross-covariance function can also be obtained by using the estimate of the cross-spectral density. The distribution of the cross-covariance function between a time series and a point process is shown to be asymptotically normal. The theoretical results are used in the study of a complex physiological system. It is shown that the presence of a gamma motor neuron (gamma stimulation) modifies the effect of the length changes on the complex system at low frequencies (the length changes, and the response of the system become uncorrelated in the range 3-30 Hz) while the effect remains unchanged at higher frequencies. As a comparison it is shown that the presence of the length changes weakens the effect of the gamma stimulation on the complex system.

Analysis of Variance↗
PubMed1991

A sensory role for the cruciate ligaments.

Morphologic, physiologic, and clinical evidence for the sensory role of the cruciate ligaments is reviewed. The cruciate ligaments accommodate morphologically different sensory nerve endings (Ruffini endings, Pacinian corpuscles, Golgi tendon organlike endings, and free nerve endings) with different capabilities of providing the central nervous system with information not only about noxious and chemical events but also about characteristics of movements and position-related stretches of these ligaments. A survey of available data reveals that low threshold joint-ligament receptor (i.e., mechanoreceptor) afferents evoke only weak and rare effects in skeletomotor neurons (alpha-motor neurons), while they frequently and powerfully influence fusimotor neurons (gamma-motor neurons). The effects on the gamma-muscle-spindle system in the muscles around the knee are so potent that even stretches of the cruciate ligaments at relatively moderate loads (not noxious) may induce major changes in responses of the muscle spindle afferents. As the activity in the primary muscle spindle afferents modifies the stiffness in the muscles, the cruciate ligament receptors, via the gamma-muscle-spindle system, may participate in the regulation and preprogramming of the muscular stiffness around the knee joint and thereby of the knee joint stiffness. Thus, the sensory system of the cruciate ligaments is able to significantly contribute to the functional stability of the knee joint.

Anterior Cruciate Ligament↗
PubMed1999

Large motor neuron involvement in Stiff-man syndrome: a qualitative and quantitative study.

Stiff-man syndrome (SMS) is characterized by fluctuating muscular rigidity and spasm. Recently, antibodies against glutamic acid decarboxylase (GAD), the enzyme catalyzing the synthesis of y-amino butyric acid (GABA), have been detected in SMS patients. An autoimmune mechanism against GAD was thus proposed for the suppression of GABAergic inhibitory interneurons, resulting in rigidity and spasm. We conducted quantitative investigations on the ventral horn of the spinal cord and its GAD immunoreactivity, post mortem, in a SMS patient and four controls. In the spinal cord of the SMS patient, we found a 70%, 33% and 27% reduction (P < 0.05) in the density of neurons with somal areas of 1000-1500 microm2, 500-1000 microm2, and 0-500 microm2, respectively. The density of neurons with a somal area greater than 1500 microm2 was not reduced, although some neurons in this class showed central chromatolytic changes. The affected muscles exhibited neurogenic atrophy. GAD-like immunoreactivity in the spinal gray matter was not significantly decreased. The density of Purkinje cells, known to contain high amounts of GAD, was not significantly reduced. While the co-occurrence of elevation of anti-GAD antibody in the serum and reduction in the density of small spinal neurons was confirmed, that of smaller alpha-motor neurons and gamma-motor neurons, the qualitative changes in larger alpha-motor neurons, and the preservation of spinal GAD-like immunoreactivity and non-spinal GAD-containing neurons suggest the involvement of factors other than autoimmune mechanisms through anti-GAD antibodies. More diverse mechanisms may be associated in the pathogenesis of SMS.

Cell Count↗
PubMed1993

Selective vulnerability of alpha motor neurons in ALS: relation to autoantibodies toward acetylcholinesterase (AChE) in ALS patients.

The degenerative process in amyotrophic lateral sclerosis (ALS) concerns primarily alpha motor neurons in the spinal cord and brain stem, and neurons forming descending pathways to the cord, especially in the pyramidal tract. Some degeneration of large peripheral sensory nerve fibers often occurs too, but preganglionic autonomic neurons and gamma motor neurons are most often spared in the disease. The vulnerability of alpha motor neurons compared to other types of neurons in ALS is discussed in relation to retrograde axoplasmic transport from peripheral blood of foreign noxious macromolecules, interneuronal transport of such molecules, and neuronal surface structure properties relevant to uptake for retrograde axoplasmic transport. Certain differences in these aspects between alpha motor neurons and other neuronal types exist. Some differences concern the neuronal turnover of acetylcholinesterase (AChE), which could be of special interest in view of the recent demonstration of regular occurrence of autoantibodies towards this enzyme in ALS patients.

Acetylcholinesterase↗
PubMed2005

Loss of synaptophysin-positive boutons on lumbar motor neurons innervating the medial gastrocnemius muscle of the SOD1G93A G1H transgenic mouse model of ALS.

Amyotrophic lateral sclerosis (ALS) is a common form of motor neuron disease (MND) that involves both upper and lower nervous systems. In the SOD1G93A G1H transgenic mouse, a widely used animal model of human ALS, a significant pathology is linked to the degeneration of lower motor neurons in the lumbar spinal cord and brainstem. In the current study, the number of presynaptic boutons immunoreactive for synaptophysin was estimated on retrogradely labeled soma and proximal dendrites of alpha and gamma motor neurons innervating the medial gastrocnemius muscle. No changes were detected on both soma and proximal dendrites at postnatal day 60 (P60) of alpha and gamma motor neurons. By P90 and P120, however, alpha motor neuron soma had a reduction of 14 and 33% and a dendritic reduction of 19 and 36%, respectively. By P90 and P120, gamma motor neuron soma had a reduction of 17 and 41% and a dendritic reduction of 19 and 35%, respectively. This study shows that levels of afferent innervation significantly decreased on surviving alpha and gamma motor neurons that innervate the medial gastrocnemius muscle. This finding suggests that the loss of motor neurons and the decrease of synaptophysin in the remaining motor neurons could lead to functional motor deficits, which may contribute significantly to the progression of ALS/MND.

Amyotrophic Lateral Sclerosis↗
PubMed1971

Histochemical and functional correlations in anterior horn neurons of the cat spinal cord.

The histochemical reaction for phosphorylase is completely lost from anterior horn neurons rich in phosphorylase within 72 hours after proximal or distal axonal section. Using this new type of axonal reaction as a marking technique in the anterior horn of the seventh lumbar spinal cord segment of the cat, we demonstrated that (i) alpha motor neurons of slow twitch motor units, like those of fast twitch motor units, are rich in phosphorylase and poor in succinate dehydrogenase, and (ii) interneurons and Renshaw neurons are rich in succinate dehydrogenase and poor in phosphorylase. Gamma motor neurons, because of their small size, are considered to be rich in succinate dehydrogenase and poor in phosphorylase. Thus, anterior horn neurons capable of higher firing frequencies (Renshaw neurons, interneurons, and gamma motor neurons) are richer in mitochondrial oxidative enzyme activity as marked by succinate dehydrogenase. Those firing at lower frequencies (both types of alpha motor neurons) are richer in phosphorylase activity and glycogen content and, thus, apparently better equipped for anaerobic glycolysis.

Animals↗
PubMed1995

The scalene reflex: relationship between increased median or ulnar nerve pressure and scalene muscle activity.

Neck pain, headaches, upper thoracic pain, and dystonic scalene muscles are common findings in patients who have severe entrapment neuropathies of the upper extremities. This problem was taken to the laboratory in an attempt to discover the correlation between distal entrapment neuropathies, brachial plexus entrapments, and prominent scalenus muscles. When increased pressure (over 40 mmHg) was applied to the median and ulnar nerves in the forelimbs of eight goats, increased electromyographic activity was noted in the ipsilateral scalenus muscle. Pressures ranging from 100 to 150 mmHg caused increased electromyographic activity on the contralateral scalene muscle, and the authors postulate that it is mediated by the gamma afferent and efferent system. This relationship may explain the commonly found neck pain and muscle spasm in patients with peripheral neuropathies, and it represents a link between the somatic efferent nerves and the gamma motor neuron system. At present, the same phenomenon has been documented in 30 humans with the diagnosis of brachial plexus entrapment.

Animals↗