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I N Beloozerova

Publications and source records attributed to I N Beloozerova.

At least 19 recordsLinked to original sources
PubMed2004

Activity of pyramidal tract neurons in the cat during postural corrections.

The dorsal side-up body orientation in quadrupeds is maintained by a postural control system. We investigated participation of the motor cortex in this system by recording activity of pyramidal tract neurons (PTNs) from limb representations of the motor cortex during postural corrections. The cat was standing on the platform periodically tilting in the frontal plane, and maintained equilibrium at different body configurations: with the head directed forward (symmetrically alternating loading of the left and right fore limbs), or with the head voluntary turned to the right or to the left (asymmetrical loading). We found that postural corrective responses to tilts included an increase of the contact forces and activity of limb extensors on the side moving down, and their decrease on the opposite side. The activity of PTNs was strongly modulated in relation to the tilt cycle. Phases of activity of individual PTNs were distributed over the cycle. Thus the cortical output mediated by PTNs appeared closely related to a highly automatic motor activity, the maintenance of the body posture. An asymmetrical loading of limbs, caused by head turns, resulted in the corresponding changes of motor responses to tilts. These voluntary postural modifications were also well reflected in the PTNs' activity. The activity of a part of PTNs correlated well with contact forces, in some others with the limb muscle activity; in still others no correlation with these variables was observed. This heterogeneity of the PTNs population suggests a different functional role of individual PTNs.

Animals↗
PubMed2003

Postural control in the rabbit maintaining balance on the tilting platform.

A deviation from the dorsal-side-up body posture in quadrupeds activates the mechanisms for postural corrections. Operation of these mechanisms was studied in the rabbit maintaining balance on a platform periodically tilted in the frontal plane. First, we characterized the kinematics and electromyographic (EMG) patterns of postural responses to tilts. It was found that a reaction to tilt includes an extension of the limbs on the side moving down and flexion on the opposite side. These limb movements are primarily due to a modulation of the activity of extensor muscles. Second, it was found that rabbits can effectively maintain the dorsal-side-up body posture when complex postural stimuli are applied, i.e., asynchronous tilts of the platforms supporting the anterior and posterior parts of the body. These data suggest that the nervous mechanisms controlling positions of these parts of the body can operate independently of each other. Third, we found that normally the somatosensory input plays a predominant role for the generation of postural responses. However, when the postural response appears insufficient to maintain balance, the vestibular input contributes considerably to activation of postural mechanisms. We also found that an asymmetry in the tonic vestibular input, caused by galvanic stimulation of the labyrinths, can affect the stabilized body orientation while the magnitude of postural responses to tilts remains unchanged. Fourth, we found that the mechanisms for postural corrections respond only to tilts that exceed a certain (threshold) value.

Animals↗
PubMed2000

Role of different sensory inputs for maintenance of body posture in sitting rat and rabbit.

In this paper, we describe the postural activity in sitting rats and rabbits. An animal was positioned on the platform that could be tilted in the frontal plane for up to +/-20-30 degrees, and postural corrections were video recorded. We found that in both rat and rabbit, the postural reactions led to stabilization of the dorsal-side-up trunk orientation. The result of this was that the trunk tilt constituted only approximately 50% (rat) and 25% (rabbit) of the platform tilt. In addition, in the rabbit the head orientation was also stabilized. Trunk stabilization persisted in the animals subjected to the bilateral labyrinthectomy and blindfolding, suggesting that the somatosensory input is primarily responsible for trunk stabilization. Trunk stabilization was due to extension of the limbs on the side moving down, and flexion of the opposite limbs. EMG recordings showed that the limb extension was caused by the active contraction of extensor muscles. We argue that signals from the Golgi tendon organs of the extensor muscles may considerably contribute to elicitation of postural corrective responses to the lateral tilt.

Animals↗
PubMed1998

Sharp, local synchrony among putative feed-forward inhibitory interneurons of rabbit somatosensory cortex.

Many suspected inhibitory interneurons (SINs) of primary somatosensory cortex (S1) receive a potent monosynaptic thalamic input (thalamocortical SINs, SINstc). It has been proposed that nearly all such SINstc of a S1 barrel column (BC) receive excitatory synaptic input from each member of a subpopulation of neurons within the topographically aligned ventrobasal (VB) thalamic barreloid. Such a divergent and convergent network leads to several testable predictions: sharply synchronous activity should occur between SINstc of a BC, sharp synchrony should not occur between SINstc of neighboring BCs, and sharp synchrony should not occur between SINs or other neurons of the same BC that do not receive potent monosynaptic thalamic input. These predictions were tested by cross-correlating the activity of SINstc of the same and neighboring BCs. Correlations among descending corticofugal neurons of layer 5 (CF-5 neurons, identified by antidromic activation) and other neurons that receive little or no monosynaptic VB input also were examined. SINs were identified by a high-frequency (>600 Hz) burst of three or more spikes elicited by VB stimulation and had action potentials of short duration. SINstc were further differentiated by short synaptic latencies to electrical stimulation of VB thalamus (<1.7 ms) and to peripheral stimulation (<7.5 ms). The above predictions were confirmed fully. 1) Sharp synchrony (+/-1 ms) was seen between all SINstc recorded within the same BC (a mean of 4.26% of the spikes of each SINtc were synchronized sharply with the spikes of the paired SINtc). Sharp synchrony was not dependent on peripheral stimulation, was not oscillatory, and survived general anesthesia. Sharp synchrony was superimposed on a broader synchrony, with a time course of tens of milliseconds. 2) Little or no sharp synchrony was seen when CF-5 neurons were paired with SINstc or other neurons of the same BC. 3) Little or no sharp synchrony was seen when SINstc were paired with other SINstc located in neighboring BCs. Intracellular recordings obtained from three SINs in the fully awake state supported the assertion that SINs are GABAergic interneurons. Each of these cells met our extracellular criteria for identification as a SIN, each had a spike of short duration (0.4-0.5 ms), and each responded to a depolarizing current pulse with a nonadapting train of action potentials. These results support the proposed network linking VB barreloid neurons with SINstc within the topographically aligned BC. We suggest that sharp synchrony among SINstc results in highly synchronous inhibitory postsynpatic potentials (IPSPs)in the target neurons of these cells and that these summated IPSPs may be especially effective when excitatory drive to target cells is weak and asynchronous.

Action Potentials↗
PubMed1993

The role of the motor cortex in the control of accuracy of locomotor movements in the cat.

1. The impulse activity of single neurones in the motor cortex (MC) was recorded extracellularly, using movable varnish-insulated tungsten microelectrodes, in six adult, freely moving cats. Neuronal activity was recorded while the cats walked on a flat floor, as they stepped over a series of barriers, and as they walked on the flat rungs of a horizontal ladder. The mean discharge rate (mR) and the depth of frequency modulation (dM) in each cell were estimated over 10-100 steps. 2. The activity of ninety-eight MC cells (Including thirteen pyramidal tract neurones (PTNs)) was recorded during stepping over barriers 25 cm apart. The mR in 66% and the dM in 61% of these cells changed by more than 20% during locomotion with barriers compared to locomotion on the flat (an increase was more often the case). 3. The activity of nine cells was recorded during stepping over barriers 12 cm apart, and the activity of twenty-seven cells (including five PTNs) during walking with barriers only 6 cm apart. The mR in 67% and in 59% of the cells, respectively, and the dM in 56% and in 67% of the cells, respectively, were greater in these locomotor tasks than during locomotion on the flat. 4. The activity of twenty cells was recorded during walking and compared in experiments with different distances between barriers. The mR in 50% and the dM in 75% of the neurones progressively increased when the distance between successive barriers was diminished. 5. The discharge rates of thirteen cells were compared in two different locomotor tasks: (i) when the cat stepped over barriers requiring hyperflexion of the limbs and (ii) when it walked on the flat with loads attached to the distal forelimbs causing a hyperactivity of flexor muscles. The activity of nine cells was different during stepping over the barriers compared to locomotion with loadings on the forelimbs. 6. The activity of 108 cells (twenty-four PTNs) was recorded during walking along a horizontal ladder with flat rungs. The mR of 61% and the dM of 72% of cells changed by more than 20% during locomotion on the ladder compared with that on the flat (most often they increased). 7. The position of the peak rate relative to the step cycle did not differ in the majority of cells (in 78-91% depending on the task) during locomotion on the flat, with the barriers or on the ladder.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1993

The role of the motor cortex in the control of vigour of locomotor movements in the cat.

1. The impulse activity of single neurones in the motor cortex (MC) was recorded extracellularly using movable varnish-insulated tungsten microelectrodes in four adult freely moving cats. The cats walked inside the experimental box with various loadings in the swing or stance phases of the step cycle. The mean discharge rate (mR) and the depth of frequency modulation (dM) in each neurone were estimated over 10-100 steps. 2. The activity of thirty-one cells (including eighteen pyramidal tract neurones (PTNs)) was recorded during uphill walking on a 10 deg inclined floor. The mR in 68%, and the dM in 77% of neurones changed by less than 20% during uphill locomotion compared to walking on a level surface. 3. The activity of the same neurones was also recorded during downhill walking, also on a 10 deg inclined plane. The mR in 69% and the dM in 78% of neurones changed by less than 20% during downhill locomotion compared with walking on a level surface. 4. The activity of twenty-three (the left hemisphere) cells (sixteen PTNs) during walking with the floor swaying to the right (R) and to the left (L) was compared to activity during locomotion on a stable surface. The mR in 83% and the dM in 83% of cells in R-steps, and in 82 and 77% of cells, respectively, in L-steps changed by less than 20%. 5. The activity of thirty-seven cells was studied during locomotion at various speeds. The mR in 68% and the dM in 38% of cells changed by less than 20% during fast and slow locomotion compared to middle-speed locomotion. The dM in 46% of neurones increased with the transfer from slow to fast walking. 6. The activity of thirty-one MC cells was recorded during locomotion with loads of 85 g attached to the distal part of each elbow. The mR in 52% and the dM in 48% of neurones changed by more than 20%. 7. The activity of twenty-eight cells (six PTNs) was studied in steps when an animal turned. The swing of the limb contralateral to the recorded MC was shorter (condition 1) in turning steps in one direction, and was longer (condition 2) in turning steps in the opposite direction. The mR in 50% and the dM in 50% of cells in condition 1 and in 52% and 59%, respectively, of cells in condition 2 changed by more than 20%.(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Physiological↗
PubMed1992

Changes in monkey horizontal semicircular canal afferent responses after spaceflight.

Extracellular responses from single horizontal semicircular canal afferents in two rhesus monkeys were studied after recovery from a 14-day biosatellite (COSMOS 2044) orbital spaceflight. On the 1st postflight day, the mean gain for 9 different horizontal canal afferents, tested using one or several different passive yaw rotation waveforms, was nearly twice that for 20 horizontal canal afferents similarly tested during preflight and postflight control studies. Adaptation of the afferent response to passive yaw rotation on the 1st postflight day was also greater. These results suggest that at least one component of the vestibular end organ (the semicircular canals) is transiently modified after exposure to 14 days of microgravity. It is unclear whether the changes are secondary to other effects of microgravity, such as calcium loss, or an adaptive response. If the response is adaptive, then this report is the first evidence that the response of the vestibular end organ may be modified (presumably by the central nervous system via efferent connections) after prolonged unusual vestibular stimulation. If this is the case, the sites of plasticity of vestibular responses may not be exclusively within central nervous system vestibular structures, as previously believed.

Adaptation, Physiological↗
PubMed1986

[Activity of neurons of the motor-sensory cortex of the cat during natural walking on the rungs of a horizontal ladder].

During locomotion on a flat surface and walking on crosspieces of a horizontal ladder the activity of 56 motor cortex neurons in the cat (5 identified cortico-spinal and 6 cortico-rubral neurons among them) was modulated in the rhythm of steps, i.e. it increased in one phase of a step and decreased in the other. The results of complication of locomotion task by the necessity of putting paws right on the support (fulcrum) while walking on the horizontal ladder were as follows: an increase of average activity of 19 neurons by 60 +/- 8% and a decrease of average activity of 19 neurons by 29 +/- 4%; growth of the modulation depth of 41 neurons (5 cortico-spinal and 6 cortico-rubral neurons) on the average by 68 +/- 19% for CS, 34 +/- 18% for CR and 36 +/- 5% for nonidentified neurons; temporary distribution of activity of 88% neurons in the step cycle while walking on the crosspieces of a horizontal ladder was that of walking on the flat surface.

Animals↗
PubMed1986

[Activity of neurons of the motor-sensory cortex of the cat during natural locomotion while stepping over obstacles].

During locomotion on flat surface and while walking with stepping over obstacles the activity of 68 motor cortex neurons in cat (there were 12 pyramidal tract neurons (PTN) among them) was modulated in the rhythm of steps, i.e. it increased in one phase of a step and decreased in the other. The results of complication of locomotion task by the necessity to swing of the limbs over obstacles were as follows: an increase of average activity of 34 neurons by 75 +/- 15% and a decrease of the activity of 20 neurons by 30 +/- 4%; growth of modulation depth of 40 neurons (9 PTN) by 35 +/- 5% on the average for non-PTN and by 67 +/- 32% on the average for PTN; temporary distribution of the activity of 81 neurons in the step cycle while walking with stepping over obstacles was that of walking on the flat surface.

Animals↗
PubMed1985

Control of locomotion in marine mollusc Clione limacina. I. Efferent activity during actual and fictitious swimming.

The marine mollusc Clione limacina swims by making rhythmic movements (with a frequency of 1-5 Hz) of its two wings. Filming demonstrated that the wings perform oscillatory movements in the frontal plane of the animal. During both the upward and downward movements of the wing, its posterior edge lagged behind the anterior one, i.e. the wing plane was inclined in relation to the longitudinal axis of an animal. As a result of this inclination, the wing oscillations in the frontal plane produce a force directed forwards. In restrained animals with the body cavity opened (a whole-animal preparation), the wing position, electrical activity in the wing nerve and activity of two identified efferent neurons (1A and 2A) were recorded during locomotory wing movements. There were two bursts of activity in the wing nerve during the locomotory cycle, the first one corresponding to the excitation of efferent neurons controlling the wing elevation, and the second one, to the excitation of efferent neurons controlling the lowering of the wing. Neurons 1A and 2A fired reciprocally at the beginning of the phase of elevating and lowering the wing, respectively. During excitation of one of the neurons, an IPSP appeared in its antagonist. A pair of isolated pedal ganglia of Clione was capable of generating the locomotory rhythm ("fictitious swimming"). In fictitious swimming, as in actual swimming, there were two bursts of activity in the wing nerve per locomotory cycle, and the 1A and 2A neurons fired reciprocally. Homologous neurons from the left and right ganglia fired inphase.(ABSTRACT TRUNCATED AT 250 WORDS)

Action Potentials↗
PubMed1985

Control of locomotion in marine mollusc Clione limacina. II. Rhythmic neurons of pedal ganglia.

Activity from neurons in isolated pedal ganglia of Clione limacina was recorded intracellularly during generation of rhythmic swimming. To map the distribution of cells in a ganglion, one of two microelectrodes was used to monitor activity of the identified neuron (1A or 2A), while the second electrode was used to penetrate successively all the visible neurons within a definite area of the ganglion. In addition, pairs of neurons of various types were recorded in different combinations with each other. Intracellular staining of neurons was also performed. Each ganglion contained about 400 neurons, of which about 60 neurons exhibited rhythmic activity related to a swim cycle. These rhythmic neurons were divided into 9 groups (types) according to axonal projections, electrical properties and the phase of activity in a swim cycle. Three types of interneurons and six types of efferent neurons were distinguished. Type 7 and 8 interneurons generated only one spike of long (50-150 ms) duration per swim cycle. Type 7 interneurons discharged in the phase of the cycle that corresponded (in actual swimming) to the dorsal movement of wings (D-phase). Type 8 interneurons discharged in the opposite phase corresponding to the ventral movement of wings (V-phase). With excitation of type 7 interneurons, an IPSP appeared in the type 8 interneurons, and vice versa. Neuropilar branching of these neurons was observed in the ipsilateral ganglion. In addition, they sent an axon to the contralateral ganglion across the pedal commissure. Efferent neurons (i.e. the cells sending axons into the wing nerve) generated spikes of 1-5 ms duration. Type 1 and 3 neurons were excited in the D-phase of a swim cycle and were inhibited in the V-phase. Type 2 and 4 neurons were excited in the V-phase and inhibited in the D-phase. Type 10 neurons received only an excitatory input in the V-phase, while type 6 neurons received only an inhibitory input in the D-phase. Type 12 interneurons were non-spiking cells, they generated a stable depolarization ("plateau") throughout most of the V-phase. Neurons of the same type from one ganglion (except for type 6) were electrically coupled to each other. There were also electrical connections between most neurons firing in the same phase of the cycle, i.e. between types 3 and 7, as well as between types 2, 4 and 8. Type 7 interneurons from the left and right ganglia were electrically coupled, the same was true for type 8 interneurons.

Action Potentials↗
PubMed1985

Control of locomotion in marine mollusc Clione limacina. III. On the origin of locomotory rhythm.

Neurons from the isolated pedal ganglia of the marine mollusc Clione limacina were recorded from intracellularly during generation of the locomotory rhythm. Polarization of single type 7 or type 8 interneurons (which discharge in the D- and V-phases of a swim cycle, respectively) strongly affected activity of the rhythm generator. Injection of depolarizing and hyperpolarizing current usually resulted in shortening and lengthening of a swim cycle, respectively. A short pulse of hyperpolarizing current shifted the phase of the rhythmic generator. The same effect could be evoked by polarization of efferent neurons of types 2, 3 and 4 which are electrically coupled to interneurons. On the contrary, polarization of types 1, 6 and 10 efferent neurons, having no electrical connections with interneurons, did not affect the locomotory rhythm. A number of observations indicate that type 7 and 8 interneurons constitute the main source of postsynaptic potentials that were observed in all the "rhythmic" neurons of the pedal ganglia. Type 7 interneurons excited the D-phase neurons and inhibited the V-phase neurons; type 8 interneurons produced opposite effects. Tetrodotoxin eliminated spike generation in all efferent neurons of the pedal ganglia, while in interneurons spike generation persisted. After blocking the spike discharges in all the efferent neurons, type 7 and 8 interneurons were capable of generating alternating activity. One may conclude that these interneurons determine the main features of the swim pattern, i.e., the rhythmic alternating activity of two (D and V) populations of neurons. Both type 7 and type 8 interneurons were capable of endogenous rhythmic discharges with a period like that in normal swimming. This was demonstrated in experiments in which one of the two populations of "rhythmic" neurons (D or V) was inhibited by means of strong electrical hyperpolarization, as well as in experiments in which interaction between the two populations, mediated by chemical synapses, was blocked by Co2+ ions. Type 7 and 8 interneurons were capable of "rebound", i.e. they had a tendency to discharge after termination of inhibition. V-phase neurons exerted not only inhibitory but also excitatory action upon D-phase neurons, the excitatory action being longer than the inhibitory one. The main experimental findings correspond well to the model of rhythm generator consisting of two half-centres possessing endogenous rhythmic activity. The half-centres exert strong, short duration inhibitory and weak long duration excitatory actions upon one another. The behaviour of such a model is considered and compared with that of the locomotor generator of Clione.

Animals↗
PubMed1985

Control of locomotion in marine mollusc Clione limacina. IV. Role of type 12 interneurons.

Type 12 interneurons in pedal ganglia of Clione limacina exerted a strong influence upon the locomotor generator during "intense" swimming. These neurons generated "plateau" potentials, i.e. their membrane potential had two stable states: the "upper" one when a neuron was depolarized, and the "down" one, separated by 30-40 mV. The interneurons could remain in each state for a long time. Short depolarizing and hyperpolarizing current pulses, as well as excitatory and inhibitory postsynaptic potentials, could transfer the interneurons from one state to another. When the pedal ganglia generated the locomotory rhythm, type 12 neurons received an EPSP and passed to the "upper" state in the V2-phase of a locomotor cycle. They remained at this state until the beginning of the D1-phase when they received an IPSP and passed to the "down" state. The EPSP in type 12 neurons was produced by type 8d neurons, and the IPSP by type 7 neurons. Type 12 neurons exerted inhibitory influences upon many neurons active in the V1 and V2 phases, and excitatory influences upon the D-phase interneurons (type 7). The functional role of type 12 neurons was to limit the activity of neurons discharging in the V-phase of a locomotory cycle. In addition, they enhanced the excitation of the D-phase neurons and promoted, thus, the transition from the V-phase to the D-phase.

Animals↗
PubMed1985

[Activity of neurons of the motosensory cortex during natural locomotion in the cat].

The activity of 42 neurons in the motosensory cortex was recorded during natural linear locomotion in two awake cats. Periodic alternations of the activity in 9 of 12 PT cells and in 13 of 30 non-PT cells were observed with respect to the locomotor cycle (modulation). The depth of the modulation of PT cells and non-PT cells was the same. The maximal-minimal activity ratio in the cycle was 16 for very modulational PT cells and was 4 for less modulational PT cells.

Animals↗
PubMed1984

[Interneuron activity of the pedal ganglia of pteropod mollusks during generation of locomotor rhythms].

Activity of interneurons from isolated pedal ganglia of marine mollusc Clione limacina was recorded during generation of the locomotor rhythm. Two groups of reciprocally active interneurons were found. These neurons generate one prolonged action potential per locomotory cycle. Inhibitory interaction between the two groups was observed. The interneurons were supposed to generate the locomotor rhythm.

Animals↗