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G A Pavlova

Publications and source records attributed to G A Pavlova.

At least 19 recordsLinked to original sources

Effects of serotonin, dopamine and ergometrine on locomotion in the pulmonate mollusc Helix lucorum.

The terrestrial snail Helix lucorum crawls using waves of muscular contraction (pedal waves) that spread along the sole of its foot. Crawling speed depends on wave generation frequency (step frequency) and the distance the snail moves forwards during each wave (step length). In a previous study, video recordings of a crawling snail showed that its sole length varied over a wide range and was directly correlated with mollusc speed. Speed depended on step length, which was directly related to sole length, rather than on step frequency, which remained rather constant. In the present study, the effects of dopamine, ergometrine (a blocker of dopamine receptors in molluscs) and serotonin injection on the linear relationship between sole length and locomotor speed in Helix lucorum were studied. In crawling snails, dopamine caused sole contraction, and locomotion slowed down or ceased. Ergometrine stimulated locomotion, which resembled rapid crawling with an extended sole, as observed under normal conditions. Serotonin stimulated locomotion and accelerated crawling significantly without causing changes in sole length. The acceleration of locomotion induced by serotonin injection was due to pedal wave (step) elongation. It is proposed that, during each locomotor episode, dopamine controls snail speed by regulating sole length, which determines the amplitude of contraction of the muscle cells involved in pedal waves and, as a result, step length; serotonin determines the basic step length and shifts the linear relationship between sole length and mollusc speed upwards along the axis of mollusc speed. The efficiency of the serotonergic system depends on the physiological state of the mollusc (e.g. that characteristic of summer or winter).

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Serotonin inhibits ciliary transport in esophagus of the nudibranch mollusk Tritonia diomedea.

Both serotonin and the molluskan pedal neuropeptides (TPEPs) cause increased ciliary beating rate of cells of the foot epithelium of the nudibranch mollusk, Tritonia diomedea. Here we compared responses of the ciliated epithelium of the esophagus with that of the foot, and report fundamental differences. Serotonin reduces the ciliary transport rate of the esophagus. We find also that the serotonin driven inhibition of esophagus is blocked and the excitation of foot epithelium is reduced by the serotonin receptor blocker ketanserin. On the contrary, ergometrine completely blocked the serotonin effect in the esophagus, and does not block the serotonin effect in the foot. Neither the TPEP driven excitation of ciliated cells of the foot nor that of the esophagus is blocked by ketanserin and ergometrine. Clearly, serotonin and TPEP regulation of different ciliated epithelia involve different receptors. Thus, mechanisms of serotonin control of different ciliated epithelia in the same animal are apparently fundamentally different, and unlike responses in all previous reports, 5HT here inhibits a ciliated epihelium.

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[Gastrointestinal complications after aortocoronary bypass].

Under analysis are gastrointestinal complications (hemorrhage, perforation of the duodenum, acute pancreatitis) which were observed in 10 of 177 patients after aortocoronary bypass. Risk factors of these complications, their specific diagnosis, treatment and prophylactics are discussed.

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Modulation of ciliary beat frequency by neuropeptides from identified molluscan neurons.

Prior work in the nudibranch Tritonia diomedea indicated that certain identifiable pedal ganglion neurons (Pd5 and 6) innervating the foot synthesize three novel peptides (TPeps) that resemble Pedal peptide (Pep) identified in the sea hare Aplysia californica. We report here that when TPeps are applied directly to isolated ciliated patches of Tritonia diomedea foot epithelium, there is an increase in ciliary beating that normally drives locomotion. Exposure to TPeps also increases the ciliary beat frequency of cells isolated from the pedal epithelium, suggesting that the observed ciliomotor effects are direct and not mediated by intervening cells. Antibodies to TPep bind to specific cells of the brain and foot and to ciliated peripheral tissues in Tritonia diomedea and in the pulmonate gastropod Lymnaea stagnalis. We suggest, therefore, that TPeps may regulate the activity of ciliated cells responsible for pedal locomotion and other functions in gastropod molluscs.

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Formation of connections between cultured identified neurones from the pleural ganglion of the pteropod mollusc Clione limacina.

A cluster of electrically interconnected neurosecretory cells (the 'white cells') involved in the control of reproductive behavior was identified in the right pleural ganglion of the marine mollusc, Clione limacina. Pleural ganglia also contain large neurons (PL1 and PL2) having no connections with each other and with the white cells. Most isolated white cells put into the simple unconditioned medium (50% L-15) adhered to the bottom of uncoated dishes and demonstrated neurite outgrowth for 7-10 days. If growing processes overlapped, the white cells formed electrical connections with each other, but they formed no connections with the PL1 and PL2 neurons. It is concluded that in the case which was under study cellular intrinsic properties were sufficient for the formation of 'correct' connections between neurones.

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Control of locomotion in marine mollusc Clione limacina. VII Reexamination of type 12 interneurons.

In previous work carried out on the isolated pedal ganglia of the pteropod mollusc Clione limacina we described the activity of a neuronal element (type 12 neuron) and looked into its role in the locomotor rhythm generation (Arshavasky et al. 1985d). As we learned subsequently, the activity was recorded from the neuron axon passing in the pedal ganglia, while the neuron soma was located in the pleural ganglia and consequently was cut off in the course of pedal ganglia isolation. It thus became necessary to reinvestigate the properties of this neuron and its role in locomotory rhythm generation by using less reduced preparation of the central nervous system. The following results were obtained. (1) Each pleural ganglion contains only one neuron of this type, this cell is thus to be considered as the identified neuron. The neuron's axon reaches into the pedal ganglion via the pleuro-pedal connective. Then the axon divides into two branches terminating in the lateral regions of both pedal ganglia. The neurons 12 from the left and right pleural ganglia have no direct connections with one another; their synchronous operation in the locomotor cycle is determined by common inputs. (2) The electrical properties of an intact neuron 12 and one without a soma are about the same. In either case the neuron generates "plateau" potentials, i.e., it may persist for a long time in the depolarized state. Plateau potentials can be induced by a depolarizing current pulse or by an EPSP, and terminated by hyperpolarizing current or by an IPSP. The neuron input resistance drops about twofold during generation of the plateau potential.(ABSTRACT TRUNCATED AT 250 WORDS)

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[Neural regulation of heart function in the Pteropod mollusc Clione limacina].

The heart of the pteropodial mollusc Clione limacina is innervated by the median nerve arising from the left abdominal ganglion. Five neurons sending axons to the heart have been identified in the Clione central nervous system with retrograde cobalt or Lucifer yellow staining. Neuron H1 located in the left pedal ganglion evoked heart excitation. Three neurons H2-H4 located in the medial part of the left abdominal ganglion caused heart inhibition. Neuron H5 located in the caudal part of the left abdominal ganglion did not affect the heart. The activity of the efferent heart neurons was found to be related to the operation of the locomotor rhythm generator. Spontaneous or reflex suppression of the locomotor rhythm generation was accompanied by inhibition of neuron H1 and excitation of neurons H2-H4. Such behavior of the efferent heart neurons ensures a positive correlation between heart and locomotor activities in Clione limacina.

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[Growth of neurites and formation of connections in cultures of pteropodial mollusc neurons].

Dissociated neurons from the brain of pteropodial mollusc were cultivated in a 25% Leibovitz medium containing 2% of calf serum. Neurite outgrowth was observed in 1-30% of the neurons. It was maximum during the first 3 days. Neurite length reached 300 microns. Membrane potential of neurons was 40-60 mV; they generated single spikes or bursts of impulses. Intercellular connections were tested on the 3-4th days in 70 pairs of neurons with neurites overlapped. Electrical connections between the cells were observed in 20% of the pairs tested, and in 6% of pairs stimulation of one of the neurons evoked an inhibitory postsynaptic potential in the other.

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Activity of C3-C4 propriospinal neurons during fictitious forelimb locomotion in the cat.

The activity of C3-C4 propriospinal neurons was recorded during fictitious forelimb locomotion in immobilized decerebrated cats with the spinal cord transected at the lower thoracic level. The discharge frequency of most neurons was rhythmically modulated in relation to the cycle of fictitious stepping in spite of the absence of any rhythmic signals from the limb receptors. Thus, the intraspinal mechanisms present a powerful input to the C3-C4 propriospinal neurons.

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Control of locomotion in marine mollusc Clione limacina. VI. Activity of isolated neurons of pedal ganglia.

In the pteropodial mollusc Clione limacina, the rhythmic locomotor wing movements are controlled by the pedal ganglia. The locomotor rhythm is generated by two groups of interneurons (groups 7 and 8) which drive efferent neurons. In the present paper, the activity of isolated neurons, which were extracted from the pedal ganglia by means of an intracellular electrode, is described. The following results have been obtained: Isolated type 7 and 8 interneurons preserved the capability for generation of prolonged (100-200 ms) action potentials. The frequency of these spontaneous discharges was usually within the limit of locomotor frequencies (0.5-5 Hz). By de- or hyperpolarizing a cell, one could usually cover the whole range of locomotor frequencies. This finding demonstrates that the locomotor rhythm is indeed determined by the endogenous rhythmic activity of type 7 and 8 interneurons. Type 1 and 2 efferent neurons, before isolation, could generate single spikes as well as high-frequency bursts of spikes. These two modes of activity were also observed after isolating the cells. Thus, the bursting activity of type 1 and 2 neurons, demonstrated during locomotion, is determined by their own properties. Type 3 and 4 efferent neurons generated only repeated single spikes both before and after isolation. The activity of the isolated axons of type 1 and 2 neurons did not differ meaningfully from the activity of the whole cells. Furthermore, in the isolated pedal commissure, we found units whose activity (rhythmically repeating prolonged action potentials) resembled the activity of type 7 and 8 interneurons.(ABSTRACT TRUNCATED AT 250 WORDS)

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[Effect of the locomotor system of the pedal ganglia of the pteropodial mollusk on anatomically isolated neurons].

The isolated pedal ganglia of the pteropodial mollusc Clione limacina generate the locomotor activity. In 30% of the pedal ganglion preparations, the locomotor rhythm was not regular, i. e. the locomotor generator worked in "bursts". These "locomotor bursts" were caused by spontaneous activations of command neurons located in the pedal ganglia. Single neurons were extracted from such preparations with an intracellular microelectrode and then their somas were put into the initial place between the ganglion cells. 25% of the isolated neurons (9 out of 35) renewed the "locomotor bursts"-related changes in the activity after the insertion into the ganglion. Neurons, originally excited during "bursts", continued to be excited after isolation, while inhibited neurons continued to be inhibited. It follows, therefore, that the command neurons can act on the target cells in the absence of morphological synapses.

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Effects of stimulation of midline inhibitory area within the pontine tegmentum on scratch reflex.

Effects of stimulation of the midline inhibitory area of the dorsal tegmental field (DTF) in the pons on the fictive scratch reflex were studied in decerebrate immobilized cats. The fictive scratch reflex was evoked by tactile stimulation of the pinna. DTF stimulation suppressed both the scratch-related rhythmical activities of the nerves (ENGs) supplying m. lateralis gastrocnemius and m. tibialis anterior, and of the interneurons at the 'leading' area of the spinal cord (L5 segment) where the scratch rhythm generator is presumably located.

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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↗

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↗

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.

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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.

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[Activity of isolated interneurons of the pedal ganglia of the pteropodal mollusk].

Interneurons from pedal ganglia of marine mollusc Clione limacina continued their rhythmical discharges for many hours after isolation. A discharge frequency increased with depolarization of neurons and decreased with hyperpolarization. It is concluded that the endogenous activity of interneurons underlies generation of the locomotor pattern in mollusc pedal ganglia.

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