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K V Baev

Publications and source records attributed to K V Baev.

At least 19 recordsLinked to original sources

Highest level automatisms in the nervous system: a theory of functional principles underlying the highest forms of brain function.

A concept that all hierarchical levels of the nervous system are built according to the same functional principles is proposed. Each level is responsible for a discrete type or set of automatisms, is a learning system, and contains two distinct functional subdivisions: (1) a controller, a subsystem providing a governing set of rules or commands-a control law-that directs the action of the recipient of these rules-the controlled object; and (2) a model, a subsystem that generates a model of object behavior, i.e. afferent information flow expected from the controlled object. A control system such as this receives two types of afferent signals-initiating and informational. The difference between these signals is that a control system minimizes initiating signals during the realization of an automatism, i.e. a control neural network utilizes informational signals to compute the proper output that minimizes the initiating input signal. A mismatch or error signal, a type of initiating signal, is responsible for learning. Both the control law and the model can be adjusted during learning. The learning process starts when the error signal increases and stops when it is minimized. A network hierarchy is structurally and functionally organized in such a way that a lower control system in the nervous system becomes the controlled object for a higher one. This hierarchy leads to a generalization of encoded functional parameters and, consequently, the working space for each higher level control system becomes more abstracted. This is the reason why each hierarchical level within the control nervous system uses detectors specific for feature of the controlled object and the environment that match the control needs in order to obtain information about the current state of the object in the environment. Movement of information toward higher hierarchical levels also is accompanied by an increase in the duration of initiating signals within each control system. The ability to store a long prehistory of preceding events is considered as the mechanism that necessitated the invention of more complex and more rapid forms of learning such as operant learning, and made possible more complex multistep computational algorithms that require memorization of the results of previous intermediate computations. The functions of the cerebellum, the limbic system and the cortico-basal ganglia-thalamocortical loops are analyzed to illustrate the utility and applicability of this theoretical concept. Basal ganglia-thalamocortical loops are described as modeling, predictive loops, and their dopaminergic innervation as an error distribution system.

Automatism↗

Disturbances of learning processes in the basal ganglia in the pathogenesis of Parkinson's disease: a novel theory.

A hypothesis is proposed that the cortico-basal ganglia-thalamocortical circuit is a neural optimal control system containing a model of the controlled object. To predict the behaviour of the object, the model uses the language of afferent signals that enter the system. Based on these ideas, it is suggested that the skeletomotor basal ganglia-thalamocortical circuit serves to model the motor behaviour of the body of an individual and its environment during motor planning and performance. Association basal ganglia-thalamocortical circuits are capable of modeling the behaviour of abstract objects such as thoughts. Within the limits of the proposed theory, the dopaminergic system serves to distribute an error signal within the striatum. These error signals contain information about mismatch between model (predicted) afferent flow and real afferent flow coming from the controlled object. An error signal is necessary to tune the model on the object, and is delivered to a structure within the circuit that is responsible for the production of the error signal. An error signal is minimal when the model properly describes the object behaviour. The process of learning is initiated when an error signal increases and is complete when the error signal is minimized. Parkinson's disease is thus considered to be the consequence of modeling disfunction because of progressive functional and structural degeneration of the error distribution system in the substantia nigra pars compacta. Other clinical applications of the proposed theory are also discussed.

Afferent Pathways↗

Novel heuristics of functional neural networks: implications for future strategies in functional neurosurgery.

A hypothesis is proposed that (a) the skeletomotor basal ganglia-thalamocortical loop functions as a model of the behavior of the body and the environment, and that (b) dopaminergic neurons of the substantia nigra pars compacta comprise the substrates of an error distribution system projecting to the striatum. This error signal initiates the learning process in the basal ganglia - learning starts with increasing intensity of the error signal and is complete when the signal is minimized. Parkinson's disease (PD) may be considered as a disruption of learning processes in the basal ganglia that results from progressive degeneration of the substrate that is the error distribution system for this functional motor loop. Numerous clinical and experimental observations obtained from functional procedures for PD that show identical clinical effects in alleviating parkinsonian symptoms, e.g. thermocoagulative lesions and chronic stimulation, can be explained through the use of this conceptual theory of basal ganglia function. Because any controlling neural network must possess a model of the behavior of its controlled object, the heuristics outlined in this theory are broadly applicable for explaining the function of the nervous system, as well as being useful for planning surgical procedures and future strategies in functional neurosurgery.

Basal Ganglia↗

Mechanisms of supraspinal correction of locomotor activity generator.

In experiments on immobilized decerebrate cats, data about reorganization of efferent activity parameters of the forelimb and hindlimb locomotor generators evoked by electrical stimulation of descending systems were obtained. The generators controlling both forelimb and hindlimb locomotor movements were found to be characterized by the existence of stable states at which total influence of different descending systems on these generators was extremely limited. These data enable us to conclude that the sense of activity reorganization in locomotor generators of both forelimb and hindlimb under the influence of descending system signals is in bringing the motor program to a dynamic relation with supraspinal inflow, where a sufficient degree of limitation and balancing of the influences of corresponding descending systems on the interneuronal nets, determining time and phase characteristics of these generators, is ensured. Possible mechanisms of realization of this interaction between descending signals and locomotor activity generators are discussed.

Animals↗

Glycine conductance changes in chick spinal cord neurons developing in culture.

Whole-cell glycine-activated currents were investigated in chick spinal cord neurons cultivated for up to three weeks. Based on the morphological and electrophysiological characteristics of neurons, two different types of nerve cells were distinguished during the first few days in culture. The first type consisted of "mature" nerve cells which appear to be motoneurons. They died by five to seven days in vitro. Immature neurons or neuroblasts constituted another type of nerve cell. They developed in culture and became differentiated neurons. Glycine-activated currents were elicited in both types of neurons during different periods in vitro. Sensitivity to glycine of "mature" neurons decreased from two to five days in vitro: ED50 for agonist action increased from 0.4 to 1.3 mM. The sensitivity of neuroblasts to this transmitter increased during differentiation: ED50 decreased from 1.4 to 0.12 mM on three to 14 days in vitro, respectively. Changes in glycine-activated conductance of these developing neurons were investigated later on. The conductance in differentiated neurons was markedly sensitive to membrane potential, while neuroblasts did not show such dependence. Voltage sensitivity was due to voltage-dependent kinetics of the ion channel. Desensitization kinetics of the glycine-activated currents were double-exponential. The time constant for the slow desensitizing component was dependent on glycine concentration, which was not the case for the fast component. The increase in glycine sensitivity of the neuroblasts was accompanied by deceleration of desensitization kinetics of the agonist-activated currents. A remarkable feature of the currents elicited in neuroblasts was their extremely long time course after rapid agonist removal from the cells. The properties of these long-term currents suggest that a large fraction of the receptors are desensitized, even during quite short applications of the transmitter. The presence of glycine in the culture medium did not affect the increase of neuronal sensitivity to the agonist. The block of spontaneous bioelectric activity by adding tetrodotoxin to the culture medium abolished developmental changes in glycine-activated conductance. Possible mechanisms for the changes in transmitter sensitivity of the neurons are considered.

Action Potentials↗

Mechanisms of supraspinal correction of scratching generator.

The influences of signals in descending systems on the parameters of scratching generator activity were studied on decerebrate immobilized cats. It was shown that phasic electric stimulation of descending systems evoked certain phase-dependent reorganization of the parameters of scratching generator efferent activity. Maximum increase in scratching cycle duration during electric stimulation of Deiters' nucleus, red nucleus and pyramidal tract is observed during stimulation in the first half of aiming phase. Stimulation in the second half of aiming phase and at the beginning of scratching jerk phase virtually does not change the scratching cycle duration. Maximum increase in scratching cycle duration during electric stimulation of the nucleus reticularis gigantocellularis is observed in the second half of aiming phase. Electric activation of descending pathways during aiming phase increases its intensity and decreases the intensity of scratching jerk phase. Activation of descending pathways during scratching jerk phase increases its intensity and virtually does not change the aiming phase intensity. Influences of electric activation of descending systems on scratching generator work reveal dependence on limb position. They are increased when the limb is deflected to the rear and are decreased during over-aimed position. Decerebellation leads to a decrease of scratching generator activity parameters rearrangement under influence of electric stimulation of the red nucleus and nucleus reticularis gigantocellularis, and to its increase during Deiters' nucleus stimulation. On the basis of these results the principles of supraspinal correction of scratching generator work are discussed.

Animals↗

Potential- and acetylcholine-activated ionic currents of pheochromocytoma PC12 cells during incubation with nerve growth factor.

Pheochromocytoma PC12 cells incubated with and without nerve growth factor were investigated using the patch-clamp technique in the whole-cell recording mode, and the concentration clamp method in the rat. On the fourth day of incubation with nerve growth factor, sodium potential-activated ionic currents appeared in the membranes of the most morphologically differentiated cells. At the same period a three-fold increase of acetylcholine-activated current density, compared with the cells incubated without nerve growth factor, was observed. Thus, the qualitative and quantitative changes in membrane properties can be a result of metabolic reorganization in PC12 cells induced by nerve growth factor and accompanied by morphological differentiation according to neuronal phenotype.

Acetylcholine↗

Primary receptor for inhibitory transmitters in lamprey spinal cord neurons.

The action of glycine and GABA on isolated lamprey spinal cord neurons was investigated by means of intracellular perfusion and concentration clamp techniques. These amino acids activated desensitizing chloride ionic conductances. The concentrations of agonists evoking half-maximum effects (ED50) were equal to 16 microM and 1.5 mM for glycine- and GABA-activated currents, respectively. Increase in the transmitter concentration led to a decrease in the time constant of desensitization. Current-voltage relationships of glycine- and GABA-activated currents were strongly dose-dependent. At low agonist concentrations the time constant of activation decreased with membrane hyperpolarization. Glycine- and GABA-activated currents exhibited complete cross-desensitization. The specific glycine antagonist, strychnine, suppressed both glycine- and GABA-activated currents to the same degree. Selective antagonists of GABA receptors, bicuculline and picrotoxin, produced equal blocking effects on glycine- as well as GABA-evoked responses. In the cells studied, taurine activated desensitizing ionic conductance. Responses evoked by taurine and glycine applications demonstrated complete cross-desensitization. Taurine-activated currents were sensitive to strychnine, bicuculline and picrotoxin. These results suggest the existence of one receptor-channel complex for the main inhibitory transmitters in lamprey spinal cord neurons. 3,4-Dioxy-L-beta-phenylalanine evoked desensitizing strychnine-sensitive ionic responses which exhibited cross-desensitization with glycine-activated currents.

Animals↗

[Relationship between the crystal lattice structure and the biological action of some agonists of amino acid receptors].

The crystal structures of glycine, taurine, GABA, beta-alanine were compared. The quantity and the accuracy of distances coincidence between nitrogen and oxygen atoms were used as a criterion of similarity of the crystalline structures. The conclusion is made about a correlation between crystalline structure of agonists and their effect on amino acid receptors. It is assumed that in case of a cooperative effect of agonist on the receptor a mutual arrangement of molecules on the receptor surface is similar to their arrangement in the agonist crystal.

Amino Acids↗

Afferent control of central pattern generators: experimental analysis of scratching in the decerebrate cat.

Systematic quantitative analysis of changes in the spinal scratching generator motor activity evoked by tonic and phasic peripheral afferent signals during "fictitious" scratching was carried out in the cat. Correlations between the kinematics of hindlimb scratching movement, sensory inflow, and primary afferent depolarization were investigated. Reliable correlations between the parameters of generator motor activity during fictitious scratching were revealed: they depended on tonic peripheral afferent inflow. The functional role of these dependencies consists of providing stability for aiming the hindlimb to the itch site. It was shown that scratching generator reaction to a phasic sensory signal depended significantly on afferent input, signal intensity, and its arrival phase in the cycle of motor activity. Phase correction of "scratching" rhythm was performed by inhibition of the current stage of "scratching" cycle, the inhibition magnitude depending on the intensity of a sensory signal run along high threshold afferent fibers. The moments in the scratching cycle, in which the afferent signal caused no rearrangement in scratching generator activity, were discovered for all investigated afferent inputs. These moments corresponded to the transitions from one scratching cycle phase to another. Integral afferent activity was distributed unevenly in the cycle during real scratching. The main part of it was observed just in that scratching cycle part which included the above mentioned no rearrangement phase points. The data obtained allowed us to conclude that the scratching generator should be considered as a working program for the motor optimal control system containing the intrinsic model of the controlled object dynamics (e.g. hindlimb scratching movement dynamics), which produces an inner analog of peripheral flow. This inner flow interacts with peripheral afferent inflow just as one of the latter components. Centrally originated modulation of primary afferent depolarization is a result of affecting the depolarization generating system by this inner "sensory" activity. It is the model, with the aid of which the generator can work after deafferentation. The functional organization of a central pattern generator is considered.

Afferent Pathways↗

Afferent control of central pattern generators: experimental analysis of locomotion in the decerebrate cat.

Changes in the motor activity of the spinal locomotor generator evoked by tonic and phasic peripheral afferent signals during fictitious locomotion of both slow and fast rhythms were analysed in the cat. The tonic afferent inflow was conditioned by the position of the hindlimb. The phasic afferent signals were imitated by electrical stimulation of hindlimb nerves. The correlation between the kinematics of hindlimb locomotor movement and sensory inflow was investigated during actual locomotion. Reliable correlations between motor activity parameters during fictitious locomotion were revealed in cases of both slow and fast "locomotor" rhythms. The main difference between these cases was that correlations "duration-intensity" were positive in the first and negative in the second case. The functional role of "locomotor" pattern dependence on tonic sensory inflow consisted of providing stability for planting the hindlimb on the ground. For any investigated afferent input the phase moments in the "locomotor" cycle were found, in which an afferent signal caused no rearrangement in locomotor generator activity. These moments corresponded to the transitions between "flexion" and "extension" phases and to the bursts of integral afferent activity observed during real locomotion. The data obtained are compared with the results previously described for the scratching generator. The character of changes in "locomotor" activity in response to tonic and phasic sensory signals was similar to that of such changes in "scratching" rhythm in the case of fast "locomotion". Intensification of the "flexion" phase caused by phasic high-intensity stimulation of cutaneous afferents during low "locomotor" rhythm was changed to inhibition (such as observed during "scratching") when this rhythm was fast. It is concluded that the main regularities of peripheral afferent control for both the locomotor and scratching generators are the same. Moreover, these central pattern generators are just working regimes of a general spinal motor optimal control system containing the intrinsic model of limb movement dynamics. The consequences of this concept and ways of further research are discussed.

Animals↗

[Effect of N-methyl-D-aspartate on the spontaneous activity generated by isolated spinal cord of 16 to 20-day-old chick embryos].

Bath-application of N-methyl-D-aspartate (NMDA) and antagonist of NMDA-receptors 2-amino-5-phosphonovaleric acid (2-APV) has been studied from the standpoint of its effect on the spontaneous activity in dorsal and ventral roots (DR and VR, respectively) generated by isolated spinal cord of 16-20-day-old chick embryo. Spontaneous activity consisted of synchronous oscillations of electrotonic potentials in DR and VR. Bath-application of NMDA (2-25 mumol/l) increased amplitude of the electrotonic potentials, induced spice discharges in DR and VR, a tonic component of electrotonic potentials. Bath-application of 2-APV (20 mumol/l) depressed spontaneous and NMDA-induced activity. The neuronal network of isolated dorsal horn (after splitting of the spinal cord) retained ability to generate spontaneous activity in DR which was intensified after bath-application of NMDA. No rhythmic activity appeared in the ventral part of the cord. The location of NMDA-sensitive neuronal network generating rhythmic (motor) activity in the spinal cord is discussed.

2-Amino-5-phosphonovalerate↗

Development of L-glutamate- and glycine-activated currents in spinal cord neurones during early chick embryogenesis.

1. The membrane currents elicited by L-glutamate and glycine applications in morphologically different neurone types were investigated in isolated spinal cord cells from the lumbar enlargement of 6 to 11-day-old chick embryos. The whole-cell patch-clamp technique and concentration clamp methods have been used. Isolated spinal cord neurones of four stages were investigated: 6, 7.5, 9 and 11 days of incubation (29th, 32nd, 35th and 37th stages of development, respectively). 2. The L-glutamate-activated conductance consisted of desensitizing and non-desensitizing components. The Hill coefficient for the first component was 1, and for the second was 2. The number of cells responding to L-glutamate application with only a desensitizing component decreased from 53.4% on the 6th day of incubation to 6.7% on the 11th day, whereas the number of cells responding with bicomponent responses increased during the same period from 13.3 to 87%. 3. From the 6th and 11th day of chick embryo development the characteristics of the desensitizing component of L-glutamate-activated conductance remained constant (half-maximal dose, (ED50 = 2.6 +/- 0.3 mM) whereas the ED50 for the non-desensitizing component decreased 10 times. 4. It was found that the density of the desensitizing L-glutamate-activated ionic current increased during morphological and age-dependent differentiation of spinal cord cells. 5. Of the investigated cells 88.7% were sensitive to glycine application. The smallest percentage of neurones responding to glycine application was observed at 7.5 days of incubation. Glycine-activated conductance did not change at the investigated stages (ED50, 71 +/- 2 microM; Hill coefficient, 2). 6. A significant decrease in the glycine-activated current density was observed on the 9th day of incubation in multipolar neurones with three neurites, against a tendency to an increase of glycine-activated ionic currents during morphological and age-dependent differentiation of cells. 7. Of the investigated cells 78% were sensitive to both glycine and L-glutamate application. A negative correlation between glycine- and L-glutamate-activated current densities (correlation coefficient, -0.71) was revealed by means of statistical analysis. 8. We conclude that these changes in chemosensitivity of the spinal cord neurones may underlie the increase in locomotor activity of the chick embryo observed on the 9th day of incubation.

Animals↗

[The action of precursors of noradrenaline synthesis on the membrane receptors of the spinal neurons in the chick embryo].

Effect of noradrenaline precursors (L-alanine, L-phenylalanine, L-tyrosine, L-DOPA and dopamine) on glycine and NMDA receptors of freshly isolated spinal neurones of chick embryo were investigated by means of the whole cell patch-clamp and concentration clamp techniques. L-alanine and L-DOPA were found to be glycine agonists which can potentiate NMDA responses. L-tyrosine does not activate glycine receptor but potentiate NMDA one. L-phenylalanine and dopamine do not interact with both glycine and NMDA receptors.

Amino Acids↗

[The restructuring of the efferent activity of the generator of scratching during the electrical activation of the descending systems].

Rearrangement of the scratching generator activity evoked by phasic electrical stimulation of different descending systems has been investigated on decerebrated immobilized cats. This rearrangement heavily depends on the stimulation phase. Maximal increase of the scratching cycle duration by electrical stimulation of Deiters' nucleus, red nucleus and pyramidal tract takes place in the first half of an aiming phase. The electrical stimulation of structures mentioned above does not practically change duration of the scratching cycle in the second half of the aiming phase and at the beginning of the scratching phase. A maximal increase of the scratching cycle duration by electrical stimulation of reticular gigantocellular nucleus occurs in the second half of the aiming phase. The electrical activation of descending pathways during the aiming phase increases intensity of this phase and decreases intensity of the scratching phase. The electrical activation of descending pathways during the scratching phase increases its intensity and does not change practically the intensity of the aiming phase. Possible principles of the suprasegmental correction of the scratching generator activity are discussed.

Animals↗