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V I Maĭorov

Publications and source records attributed to V I Maĭorov.

At least 19 recordsLinked to original sources
PubMed2004

[Structure and expression of the F6.2 gene in Chironomus thummi and other Chironomus species].

A full-length copy of the F6.2 gene from the tissue-specific BRa locus of the Chironomus thummi chromosome IV was isolated and analyzed. The gene contains two exons (715 and 644 bp, respectively) and one 172-bp intron. The data of the RT-PCR analysis demonstrated that F6.2 was transcriptionally active at different developmental stages of Chironomus thummi and at least in the last larval stage of C. dorsalis. The distribution of the F6.2 gene among 42 species of Chironomus, as well as among two other genera of the family Chironomidae was examined by means of PCR. The F6.2 sequence was found in 34 Chironomus species. Using in situ hybridization, three species were analyzed for the presence of the F6.2 homologous sequences. In five species, the sequence of the F6.2 PCR product was determined. In these species, the intron size polymorphism caused by the variation of the number of the intron-forming repeats was observed. The data obtained provided evaluation of the F6.2 distribution among the genus Chironomus.

Amino Acid Sequence↗
PubMed1977

[Transformation of an afferent tactile signal into a motor command in the cat motor cortex].

The activity of 112 units of the cat precruciate motor cortex was studied simultaneously with the performance of a placing reaction of the foreleg to tactile stimulation of its distal parts. The response latency to the tactile stimulation of the foreleg was 30-40 ms for the electromyographic response of m. biceps brachii and 20 +/- 10 ms for the earliest-responses of the motor cortical neurons. The electrical reaction of m. biceps brachii occured 5-10 ms after the termination of the electrical stimulation of the cortex by a puls series (the series duration was 25 ms, the pulse duration 0.2 ms, frequency 400 per s). Two different types of excitatory reactions of the motor cortex units were found: the sensory (s) ones occured at each tactile stimulus and did not depend on the presence or absence of the foreleg motion; the motor (m) type of reactions developed simultaneously with the motor placing reaction of the foreleg only. The minimal latency of cortical m- and s-type discharge was 20 +/- 10 ms. Electrical stimulation (5-25 micronA) through the microelectrode placed in the locus of neuronal activity which increased during active flexion of the foreleg, provoked in 70% of cases the electrical response in m. biceps brachii.

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[The reactions of the cat motor cortex neurons to electrical stimulation of the base of the forebrain as a conditioned signal for the reflex of placing the forelimb on a support].

Electrical stimulation of the globus pallidus (500 ms, 300 Hz) in the area restricted by the stereotaxic coordinates AP 14-AP 16, L5-L8 at the level of the anterior commissura (HO) evoked food reactions in the form of mouth opening, chewing, and licking in the absence of food. There were no visible motor effects in the case of electrical stimulation of the subcommissural area (H-2-H-4) corresponding to the ventral pallidum and substantia innominata. The conditioned forepaw placing reaction was elaborated with the basal forebrain stimulation used as a conditioned stimulus. After conditioning, the short (3-5 pulses) conditioned basal forebrain stimulation evoked a prolonged (up to 500-1000 ms) activation of neurons in the motor cortex. This activation did not change in the absence of the movement, i.e., after acute extinction of the contralateral forepaw placing or transfer of placing reaction to the ipsilateral forepaw.

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[The neuronal reactions of the cat motor cortex to electrical stimulation of the ventral tegmental area as a conditioned signal for the reflex of placing the forelimb on a support].

Electrical stimulation (50-100 pulses, 100-500 Hz) of the ventral tegmental area (VTA) in the vicinity of the n. interpeduncularis in the frontal plane AP2-AP4, L1-L2 caused a cat to grab food placed near its mouth. The conditioned forepaw placing reaction was elaborated using food reinforcement and VTA stimulation as a conditioned stimulus. The conditioned reflex, being once established, was repeatedly performed without extinction in the course of up to 250 trials without food reinforcement. Short (5-10 pulses) conditioned VTA stimulation evoked a prolonged (up to 1000 ms or longer) activation of neurons of the motor cortex and caused a substitution of the inhibitory phase of response to stimulation of the parietal cortex in poststimulus interval in 50-200 ms for the late secondary excitatory response.

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[The long-term potentiation of the late NMDA-dependent components of the responses of the cat motor cortex neurons to stimulation of the direct cortical input of area 5 in the parietal cortex].

Activity of neurons in the motor cortex was recorded in anesthetized cats with glass micropipettes filled with bicuculline solution (bicuculline methiodide, 10 mM in 1 M NaCl). Under these conditions, the minimal (near-threshold) electrical stimulation of the area 5 of the parietal cortex evoked the late neuronal discharges (in 30-200-ms poststimulus interval) in the motor cortex. Such discharges resembled the late NMDA-dependent discharges recorded in the motor cortex of awake cats in response to stimulation of the parietal cortex, which produced the preliminary elaborated conditioned forepaw placing. Under the same conditions, tetanic stimulation of the parietal cortex (100 Hz, 10-20s) led to the long-term potentiation of the late response, which manifested itself as response amplitude augmentation and latency shortening.

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[The late excitatory responses of the motor cortex neurons in the cat to stimulation of the pyramidal tract].

Under conditions of partial suppression of GAMKA-dependent cortical inhibition in the motor cortex of anesthetized cats, a weak electrical stimulation of the pyramidal tract evoked the late slow (50-200 ms) excitatory reactions in the motor cortex neurons similar to those previously recorded under the same conditions in response to stimulation of the parietal cortex. This finding favors the proposal that the late excitatory component of the cortico-cortical response reflects the repetitive activation of cortical neurons due to excitation spread via the system of cortical recurrent excitatory collaterals.

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[NMDA-dependent and NMDA-independent neuronal processes in the cat motor cortex, disinhibited by bicuculline, during forepaw placement conditioning].

Neuronal activity associated with a conditioned forepaw placing reaction was recorded in the cat's motor cortex locally disinhibited by bicuculline spontaneously diffused from the recording pipette. Electrical stimulation of the parieral cortex (area 5) with 3-5 pulses was used as a conditioned stimulus. In both naive and trained cats, adding of APV (NMDA receptor blocker) led to disappearance of the late (30-120 ms) secondary excitatory responses from the pattern of the neuronal reaction to the parietal stimulation recorded in the motor cortex. At the same time, the APV administration did not change the excitatory reactions (recorded, predominantly, in the deep cortical layers) time-locked to the execution of the conditioned movement. The conditioning resulted in a statistically significant increase in the amplitude and duration of the late secondary responses as well as in a shortening of their latency. In some cases (after a long period of training), the late secondary responses to the conditioned stimulus transformed into paroxysmal epileptiform bursts. A hypothesis is discussed that the increase in synaptic strength of the backward horizontal collaterals of layer-II/III pyramidal neurons is responsible for the learning-related changes in the neuronal reactions in the disinhibited motor cortex.

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[Correlation between different forms of trace phenomena in the activity of rabbit visual cortex neurons].

Plastic changes in the components of the unit responses in the rabbit visual cortex (VC) in the course of electrical stimulation (with different parameters) of the lateral geniculate body (LGB) were compared with the capacity of the same units for trace driving to the LGB preceding stimulation. Potentiation of inhibition (inhibitory pauses) in reponse to electrical LGB stimulation is the main plastic phenomenon in the activity of VC units. Trace driving is characteristic predominantly of units with enhanced plasticity of the excitatory sign, a tendency toward epileptiform activity after LGB tetanization. In most cases inhibitory reaction is expressed in weakening of the periodic component of neuronal activity corresponding to the frequency of stimulation. The level of trace suppression of periodicity positively correlates with potentiation of the inhibitory pause during prolonged LGB stimulation.

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[Models of learning based on the plastic properties of the "placing reaction" in cats].

A possibility of functional reorganization of initial sensorimotor connections of the forepaw has been shown on seven cats. The main initial relationships between the afferent tactile input and motor output for the ulnar joint of the cat forepaw are as follows: tactile stimulation of the dorsal surface of the paw produces a flexion in the ulnar joint ("placing reaction"), and that of the ventral surface, an extension of the paw in the ulnar joint ("magnetic reflex"); simultaneous tactile stimulation of the ventral surface of the paw blocks the "placing reaction" evoked by a touch of the dorsal side. Extinction was produced of the above unconditioned connections and elaboration of a new "cross" connection consisting in that tactile stimulation of the ventral side of the paw resulted in flexion in the ulnar joint.

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[A computer model of generation of the motor cortex neuron processes seen in the course of execution of instrumental movement].

A computer model of neuronal processes in the motor cortex column is presented. The model is consisted of two pyramidal cell layers with two groups of inhibitory interneurons, selectively controlling pyramidal cell soma and dendrite, in each. Active Na, Ca and K conductances are included in the model of a single neuron. Horizontal excitatory connections between pyramidal cells in the upper layer are largely of NMDA-receptor type, that in the lower layer--of non-NMDA-type. All inhibitory synapses are of GABA(A)-type. The model reproduces the main phenomenon observed in the motor cortex during the execution of conditioned movements. Consequent to an early excitation the upper layer pyramidal cells generate a late NMDA-dependent reflexive response to afferent conditional stimulation, which as in a real case is diminished by GABA(A)-type synaptic inhibition and afferent stimulus strength increase. The characteristic inverse relation between the late response manifestation and the stimulus strength observed in the real cortex can be reproduced in the model only if NMDA-glutamate receptors were preferentially localized in the terminals of pyramidal cell backward collaterals, not in the terminals of the afferent fibers on pyramidal neurons. The intended component of motor cortex neuronal activity is generated in NMDA-independent manner by the pyramidal cells of lower layer. The slow time coarse of intended component as compared with short duration of AMPA epsp's is due to a consecutive relay-race--like activation of pyramidal neurons with different dendrit-to-soma ratio.

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[The blockade of D1 dopamine receptors in cat motor cortex causing an increase in the latency of conditioned forelimb placing reaction].

Cat were trained to place a forepaw on a support in response to touching the ventral surface of the forepaw as a conditioned stimulus. A selective D1 receptor antagonist SCH23390 was injected under pressure into the region of pericruciate cortex just anterior and lateral to the end of the cruciate sulcus. Electrical microstimulation of this region evoked the elbow flexion and shoulder withdrawal that constitute the initial lifting--withdrawal phase of the forepaw placing. In contrast to control saline, the injection of SCH23390 caused a gradual increase in the latency of conditioned placing so that to the end of experiment it was, on the average, 200 ms longer than its preinjection level. The results obtained show that the local D1 receptor blockade in cat motor cortex significantly increases the latency of the simple instrumental conditioned reflex.

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[The activity of cat motor cortex neurons during performance of a conditoned response of placing the forepaw on a support].

The activity of 74 units of the cat precentral motor cortex was studied in the process of reaction of placing the forepaw on a support. It has been shown that the neurones controlling the flexion of the ulnar joint, the first phase of the reaction, receive an afferent tactile input primarily from the dorsal side of the paw, i.e. from region of the skin surface which is the receptive field of the reflex of placing the paw on the support. Learning the animals to lift the paw to the support in response to a touch of the ventral surface results in an increase of discharge frequency of the studied units in response to ventral stimulation similar to that recorded in response to the initially effective dorsal stimulation.

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[Local disinhibition with bicuculline does not break the trained relationship between afferent input and efferent output in cat motor cortex].

Neurons of the cat motor cortex related to the lifting-withdrawal phase of forepaw placing reaction are preferentially activated by tactile stimulation of the dorsal surface of the forepaw. The placing reaction was altered in such a way that the innate "dorsal placing" was subjected to extinction and was substituted for the newly acquired conditioned reaction in response to the ventral side stimulation. This alteration of placing reaction led to the inversion of the innate input-output relationship in the motor cortex. The neurons related to forepaw lifting-withdrawal began to be activated by tactile stimulation of the ventral rather than dorsal forepaw surface. Local cortical disinhibition by bicuculline application at the recording site qualitatively changed neither normal input-output relationships nor inverse relationships after placing reaction alteration. This suggests that alteration of the sensorimotor coordination in cat motor cortex is underlain by changes in excitatory rather than inhibitory connections.

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[Long-latency responses to conditioned stimulus in the cat motor cortex can be generated through the enhancement of efficiency excitatory collaterals of pyramidal neuron].

The long-latency excitatory components are the characteristic feature of neuronal responses to conditional stimuli in the motor cortex of the cat. The data presented suggest that the neuronal machine that generates these reactions is that, generating long-latency epileptiform discharges in epileptogenic cortex. The long-latency component generation is based on NMDA-receptor activation in the recurrent excitatory collaterals of the cortical pyramidal neurons. The response delay is dependent on initial activation of inhibitory GABA(A) receptors. The emergence of the late components in the course of motor learning take place as a result of efficiency enhancement of recurrent collaterals synaptic linkage with pyramidal neurons.

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PubMedDate not supplied

[Analysis of hippocampal participation in organizing animal behavior].

Based on some properties of hippocampal circuitry, an attempt has been made to interpret behavioural changes in hippocampectomized animals. The regulation of cortically initiated information flow through the hippocampus by the unspecific inhibitory blocking, selective depression or potentiation of intrinsic hippocampal chains has been analyzed at different levels of reticulo-septal input, characteristic of different behavioural patterns. By the first mode of hippocampal regulation the ignorance of irrelevant stimuli during an automatized behaviour is achieved; temporary selective depression or strengthening of influence of certain relevant stimuli takes places in the two other modes.

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