Spatial organization of inhibitory control of activity of vestibulospinal Deiters' neurons by Purkinje cells in the anterior lobe of the cerebellum

The topographical distribution of vestibulospinal neurons in Deiters' nucleus was investigated by a microelectrode method. By contrast with observations made in morphological experiments, the localization of antidromically identified vestibulocervical (C-neurons) and vestibulolumbar (L-neurons) cells was found not to be limited to the ventral middle and rostral third of the nucleus (the forelimb region) and caudodorsal part of the nucleus (hind limb region), but to include the whole of the ventral and dorsal half of the nucleus, respectively. The zones of localization of these two groups of neurons are not confined to a single layer: C-neurons are found in the dorsal half of the nucleus and L-neurons in its ventrocaudal part also. Analysis of the distribution of monosynaptic IPSPs arising in response to activation of Purkinje cells in the vestibulospinal neurons showed that C-neurons are controlled chiefly from the forelimb zone of the cerebellar cortex whereas L-neurons are controlled equally by inhibitory influences from the forelimb and hind limb zones of the anterior lobe of the cerebellar cortex.L. A. Orbeli Institute of Physiology, Academy of Sciences of the Armenian SSR, Erevan. Translated from Neirofiziologiya, Vol. 11, No. 1, pp. 54–64, January–February, 1979.     

The role of different size vestibulospinal neurons in the static control of posture

1. In addition to giant cells, originally described by Deiters, the lateral vestibular nucleus contains also medium- and small-size cells. The role that these neurons exert in the static control of posture has been investigated in precollicular decerebrate cats in which the resting discharge of spontaneously active vestibulospinal neurons projecting to lumbosacral segments of the spinal cord (IVS neurons) has been related to the cell size inferred on the basis of the conduction velocity of their axons. 2. In control experiments, the IVS neurons with slower axonal conduction velocity and, by inference, having thinner axons and smaller cell bodies differed from those having faster conduction velocity by displaying a higher resting discharge rate and a relatively regular interspike interval distribution, i.e. a lower coefficient of variation (CV). 3. The resting discharge of the IVS neurons, which corresponded on the average to 24.5 +/- 15.7, S.D. imp./sec, in control experiments, increased significantly to 44.1 +/- 23.8, S.D. imp./sec after ablation of the cerebellar vermis and the fastigial nuclei, leading to a great increase in postural activity, while the proportion of regularly discharging units (with the lowest CV) increased. Moreover, the negative correlation between resting discharge of all the recorded IVS neurons and the conduction velocity of the corresponding axons, which was quite slight in the experiments with the cerebellum intact, greatly increased after partial cerebellectomy. This finding was due to a prominent increase in resting discharge of the small-size IVS neurons, while the discharge of the large-size IVS neurons was, on the average, comparable to that obtained in the controls. It appears, therefore, that the cerebellum exerts a prominent tonic inhibitory influence on the small-size IVS neurons, which are thus responsible for the great increase in decerebrate rigidity after cerebellectomy. 4. The resting discharge rate of the IVS neurons was not, on the average, greatly modified after ipsilateral acute (aVN) and chronic vestibular neurectomy (cVN) with respect to the controls. However, the proportion of regularly discharging units (with the lowest CV) decreased after aVN, but increased after cVN. The relation found in control experiments, i.e. the faster the conduction velocity of VS axon the lower was the unit discharge at rest, was lost after aVN, due to a decrease in resting discharge rate of the slow neurons. The mean discharge rate of these units, however, recovered after cVN, so that the negative correlation between resting discharge rate and axonal conduction velocity was reestablished.(ABSTRACT TRUNCATED AT 400 WORDS)     

Morphology of lumbar-projecting lateral vestibulospinal neurons in the brainstem and cervical spinal cord in the squirrel monkey

The lateral vestibulospinal tract (LVST) is one of the major descending pathways controlling the extensor musculature of the body. To determine whether individual LVST neurons terminating in the lumbosacral spinal segments issue collaterals more rostrally to exert an influence of the cervical ventral horn intracellular recording and biocytin labeling techniques were used in the squirrel monkey. Only neurons monosynaptically related to the 8th nerve and antidromically identified to project below T12 were selected for study. The axon course through the brainstem and cervical spinal cord was examined in 37 LVST neurons. The average distance of recovered axon was 17.3 mm (4.5-31.7 mm). None could be antidromically activated from shocks applied to the rostral medial longitudinal fasciculus near the 3rd nuclei; and no collaterals were observed in the brainstem. Of the 37 neurons, only 1 axon issued a collateral to innervate the ventral horn, primarily in the region of the spinal accessory motoneurons; this single collateral provided a relatively minor input compared to that of LVST neurons terminating in the cervical cord. Thus, secondary, caudal-projecting LVST neurons represent a private, and mostly rapid, communication pathway between dorsal Deiters' nucleus and the motor circuits controlling the lower limbs and tail.     

Classification of vestibulo-spinal neurons of the cat Deiters' nucleus

Antidromic excitation of neurons of the lateral vestibular nucleus of Deiters in cats in response to stimulation of the vestibulo-spinal tract in the cervical segments of the spinal cord was studied by intracellular microelectrode recording. Individual components of the antidromic action potential and accompanying after-potentials were analyzed and fast and slow neurons distinguished. The vestibulo-spinal neurons were differentiated on the basis of after-potentials accompanying the antidromic action potential. The ratio between fast and slow neurons differed in individual groups. The parameters of the depolarization after-potentials were directly proportional to the duration of the refractory period of the neurons studied. An attempt was made to correlate differences in the responsiveness of neurons with an identical conduction velocity along their axons with the characteristics of the depolarization after-potential.     

Spatial organization of vestibulospinal neurons in the guinea pig

Quantitative characteristics of spatial organization of neuron populations of vestibular nuclei, forming projections into the spinal cord, were obtained in experiments on guinea pigs by the retrograde axonal transport of horseradish peroxidase, injected unilaterally into the upper cervical and lower thoracic segments of the spinal cord, method. Neurons accumulating the enzyme were found ipsilaterally in the lateral vestibular nucleus and bilaterally in the descending and medial vestibular nuclei. The distribution of vestibulospinal neurons along the length of the spinal cord was studied. Neuron populations of the medial and descending vestibular nuclei whose projection regions coincide with those of fibers of the corticospinal and rubrospinal systems were discovered. The role of vestibulospinal systems in the structure of supra-segmental control of the neuronal apparatus of the spinal cord is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 23, No. 3, pp. 353–362, May–June, 1991.     

Effect of quinolinic acid on neurons in dissociated cultures of cells of different structures of the brain

Using neurohistological and cytochemical methods in the living cells, the peculiarities of the action of endogenous neurotoxin, quinolinic acid (QUIN), on the neurons developing in the cell cultures of the hippocamp, neocortex and septum have been investigated in 17-19-day-old mouse embryos. The addition of 500 microM of QUIN on the 21st--22nd day into the nutrition medium in vitro resulted in the rapid destruction of neurons localized in glioneuronal aggregates, while the isolated nervous cells as well as septal cholinergic neurons remained intact. At earlier stages of cultivation (up to 2 weeks) QUIN did not provoke degenerative changes in the cultivated neurons. The comparison of our results with the literary data suggests that in nervous cell cultures QUIN, having mature synaptic connections with afferent nervous fibers, causes destruction of neurons.     

Reticulospinal and vestibulospinal synaptic effects on the lumbar motor neurons of the monkey

It was established in experiments on rhesus monkeys by intracellular recording and computer averaging that fast-conducting reticulo- and vestibulospinal fibers form monosynaptic excitatory links with lumbar alpha-motor neurons. The monosynaptic bulbospinal effects are retained after sectioning of the pyramids or after chronic destruction of the motor cortex. The mean amplitude of the reticulomotor neuronal EPSP is less than that of the corticomotor neuronal EPSP, however, the mean amplitudes of the EPSP of individual motor neurons can reach similar values. In contrast to the corticomotor neuronal projections, the bulbomotor neuronal projections are directed primarily toward the motor neurons of the proximal muscles. In addition to monosynaptic EPSP, reticulo- and vestibulospinal impulses evoke disynaptic EPSP and IPSP in the lumbar motor neurons of monkeys which are very similar to the disynaptic effects found in subprimates.I. M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Academy of Sciences of the USSR, Leningrad. Translated from Neirofiziologiya, Vol. 3, No. 4, pp. 408–417, July–August, 1971.     

Electroencephalographic analysis of inter-central relations in hypothalamo-reticulo-limbic brain structures during treatment with corticosteroids and neuropeptides

Intercentral relations between hypothalamus, limbic system and reticular formation were studied in rabbits and rats under systemic and central action of DSIP, ACTH, corticosteroids and stress (aggressive-defensive behaviour). The results obtained demonstrate changes in the adrenal cortex resulting from stress-inducing adrenocortical hormone content. The increase was achieved by the rise in ACTH level resulting in corticosteroid level elevation (endogenous elevation-aggressive behaviour) and by corticosteroid injections (exogenous elevation). Correlation analysis of structural interrelations after ACTH and corticosteroid injections demonstrated an increased correlation between hypothalamo-reticular-limbic structures. DSIP was shown to have an opposite effect. Correlation analysis revealed the potentials for the formation of new functional interrelations between hypothalamo-reticular-limbic structure in the motivation of aggression (stress) and the levels of corticosterone and DSIP. DSIP action depends on the initial corticosteroid blood level and is more marked in stress-inducing concentrations.     

Stimulation of midbrain dopaminergic structures modifies firing rates of rat lateral habenula neurons

Ventral tegmental area (VTA) and substantia nigra pars compacta (SNpc) are midbrain structures known to be involved in mediating reward in rodents. Lateral habenula (LHb) is considered as a negative reward source and it is reported that stimulation of the LHb rapidly induces inhibition of firing in midbrain dopamine neurons. Interestingly, the phasic fall in LHb neuronal activity may follow the excitation of dopamine neurons in response to reward-predicting stimuli. The VTA and SNpc give rise to dopaminergic projections that innervate the LHb, which is also known to be involved in processing painful stimuli. But it's unclear what physiological effects these inputs have on habenular function. In this study we distinguished the LHb pain-activated neurons of the Wistar rats and assessed their electrophysiological responsiveness to the stimulation of the VTA and SNpc with either single-pulse stimulation (300 μA, 0.5 Hz) or tetanic stimulation (80 μA, 25 Hz). Single-pulse stimulation that was delivered to either midbrain structure triggered transient inhibition of firing of ～90% of the LHb pain-activated neurons. However, tetanic stimulation of the VTA tended to evoke an elevation in neuronal firing rate. We conclude that LHb pain-activated neurons can receive diverse reward-related signals originating from midbrain dopaminergic structures, and thus participate in the regulation of the brain reward system via both positive and negative feedback mechanisms.     

Distribution of different types of calcium channels in the brain structures

This study demonstrates that low voltage-activated (LVA) Ca²⁺ channels and at least five pharmacologically distinct high voltage-activated (HVA) Ca²⁺ channels exist in most rat CNS neurons, with the exception of cerebellar Purkinje cells. These LVA and HVA Ca²⁺ channels (including their subtypes) are differentially distributed among various CNS regions. The pharmacological diversity of these channels and their heterogeneous distribution on the nerve cell somata and nerve endings appear relevant in the development of new and region-specific pharmacological agents for clinical use.     

The presence of phosphatidylcholine in neurons isolated from the lateral vestibular nucleus of ox brain

1. Lipid was extracted from neurons isolated from the lateral vestibular nucleus of ox brain and examined by two-dimensional thin-layer chromatography. 2. The major lipids found were phosphatidylethanolamine and its plasmalogen, phosphatidylcholine, phosphatidylserine and cholesterol.     

Creatine phosphokinase BB distribution in different structures of the human brain

Regional localization of creatine phosphokinase BB was studied in postmortem human brain and its stability was shown. The content of CPK BB in different brain structures was unequal: from 0.5 mcg/mg of protein in the occipital lobe and tuber cinereum to 4.5 mcg/mg in the frontal lobe. In the regional localization of CPK BB in the postmortem brain of schizophrenia patients, some changes in isoenzyme content were found as compared to the control group. The reduction of CPK BB concentration at schizophrenia was found in the frontal lobe (45%, P less than 0.001) and s. nigra (70%, P less than 0.001); the concentration was higher in the thalamus and occipital lobe (15%, P less than 0.001), as well as in the parietal lobe, cingulate gyrus, tuber cinereum, cerebellum cortex, inferior olive--50-80%, P less than 0.001.