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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 78 (1989), S. 398-406 
    ISSN: 1432-1106
    Keywords: Pteropod mollusc ; Locomotion ; Central pattern generator ; Interneurons ; Plateau potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 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. (3) Recording of the neuron 12 in the pleural ganglia showed that its activity during “fictive swimming” does not differ from that of somadeprived axon recorded in the isolated pedal ganglia. The neuron generates a plateau potential in the V-phase of the locomotor cycle (definitions for the phases of the cycle were given in Arshavsky et al. 1985b). This potential is triggered by an EPSP evoked by subgroup 8d pedal neurons. The plateau potential terminates in the D-phase under the influence of an IPSP evoked by group 7 neurons. The effects of the neuron 12 on other neuronal elements of the locomotor generator in pedal ganglia do not depend on the presence of the cell soma either. (4) The pedal ganglia locomotor generator sometimes generates an “anomalous rhythm” when normal cycles alternate with reduced ones in which the activity of some groups of neurons is inhibited. Simultaneous recording from two neurons 12 demonstrated that the alternating rhythm generation was caused by the anomalous behaviour of one of the neurons 12: the neuron persisted in the depolarized state for one cycle and a half and not for half a cycle, as during the normal operation of the locomotor generator.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Pteropodial mollusc ; Locomotion ; Pedal ganglion ; Interneurons ; Efferent neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1.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. 2.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. 3.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. 4.Efferent neurons (i.e. the cell 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. 5. Type 12 interneurons were non-spiking cells, they generated a stable depolarization (“plateau”) throughout most of the V-phase. 6. 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.
    Type of Medium: Electronic Resource
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