Impulse Activity and Pattern of Large and Small Neurones in the Cardiac Ganglion of the Lobster, Panulirus Japonicus

1973 ◽  
Vol 58 (2) ◽  
pp. 473-486
Author(s):  
KENRO TAZAKI

1. Single-unit analysis was made by means of internal and external recordings in order to observe the impulse activity of the component neurones in the lobster cardiac ganglion. 2. The large cells fired a brief high-frequency train of postsynaptic impulses in the axonal region by repetitive synaptic activation from small cells which was brought about in the soma-dendritic regions. They generated slow potentials with repetitive impulses by themselves when without synaptic controls. 3. A long-lasting train of presynaptic impulses was propagated from the small pacemaker neurone to the large-cell somata, inducing small synaptic potentials. The burst activity of the ganglion was initiated by this neurone. 4. Impulses of different kinds, presynaptic or postsynaptic, were observed in small cells. This activity occurred at about the same time as that of the pacemaker neurone and was of almost the same duration. 5. Synchronizing mechanisms of all nine neurones were discussed with respect to electrotonic interaction mediated by slow potentials, compared to synaptic interaction mediated by impulses.

1972 ◽  
Vol 57 (3) ◽  
pp. 713-726
Author(s):  
KENRO TAZAKI

1. Various patterns of burst activity in the cardiac ganglion cells of the crab Eriocheir japonicus were observed by means of intracellular electrodes. 2. The pacemaker for burst initiation is located among small cells, and it induces small synaptic potentials in the large cells, increasing their excitability. The anterior large cells generate slow potentials by synaptic activation. 3. The slow potential is the spike generator. The anterior large cells are capable of initiating slow potentials in their own somata without synaptic activation from the small cell. 4. Non-synaptic maintained depolarization takes place in the anterior large cell membrane. The after-depolarization are cumulative and can develop the slow potential, leading to repetitive firing. 5. The posterior large cell is innervated by two pre-synaptic nerve fibres, one being the small pacemaker cell and the other the anterior large cell, showing that it is a follower. 6. Electrical interaction is present among ganglion cells. Positive feedback through electrical connexions is observed between large and small cells. 7. The cardiac ganglion of the crab has some features common and similar to those found in the ganglia of both the lobster and Squilla.


1975 ◽  
Vol 63 (1) ◽  
pp. 33-52
Author(s):  
I. M. Cooke ◽  
D. K. Hartline

The spontaneous burst discharges of isolated lobster (Homarus americanus) cardiac ganglia were recorded with a spaced array of electrodes. Small regions (less than 1 mm) of the ganglion were exposed to the cardioexcitor neurohormone in extracts of pericardial organs (XPO) or to 10(−5) M 5-hydroxytryptamine (5HT). All axons were excited (increased mean firing frequency, f) by both substances, but only by applications in the region between the soma (but excluding it) and proximal site of impulse initiation. Units not so exposed changed their f relatively little despite f increases of as much as threefold in exposed units and changes in burst rate and overall length. Regularity and grouping of all impulse activity into bursts was never disturbed. 5HT increases burst rate at any point of application. The increases are larger if small cells are affected than if only large cells are exposed. Burst length decreases except when the pacemaker is affected. In contrast, XPO affects neither burst rate or length unless small cells are affected. Length is increased if non-pacemaker small cells are affected; both rate and length increase if the pacemaker is affected. The pacemaker usually exhibits an f of intermediate value. Rate changes are not simply related to its f. A small cell can “burst” in the absence of impulses from any other cells. XPO may enhance endogenous “driver potentials,” while 5HT may excite by depolarizing at limited sites.


1973 ◽  
Vol 62 (4) ◽  
pp. 448-472 ◽  
Author(s):  
Earl Mayeri

External recording and stimulation, techniques were used to determine which neurons and interactions are essential for production of the periodic burst discharge in the lobster cardiac ganglion. Burst activity can be modulated by brief single shocks applied to the four small cells, but not by similar stimulation of the five large cells, suggesting that normally one or more small cells primarily determine burst rate and duration. Repetitive electrical stimulation of large cells initiates spike activity in small cells, probably via excitatory synaptic and/or electrotonic connections which may normally act to prolong bursts and decrease burst rate. Transection of the ganglion can result in burst activity in small cells in the partial or complete absence of large cell spike activity, but large cells isolated from small cell excitatory synaptic input by transection or by application of dinitrophenol do not burst. Generally, transections which decrease excitatory feedback to small cells are accompanied by an increase in burst rate, but mean spike frequency over an entire burst cycle stabilizes at the original level within 10–30 min for various groups of cells whose spike-initiating sites are still intact. These and previous results suggest that the system is two layered: one or more small cells generate the burst pattern and impose it on the large cells which are the system's motorneurons.


1984 ◽  
Vol 109 (1) ◽  
pp. 121-140 ◽  
Author(s):  
TAKETERU KURAMOTO ◽  
ARINOBU EBARA

1. Systolic contractions of the isolated heart were usually composed of a first and second systolic contraction (FSC and SSC) which corresponded to the first and second large potentials (FLP and SLP), respectively, recorded in the cardiac muscle cells and represented excitatory junction potentials produced by impulse bursts of the large cells of the cardiac ganglion. 2. Under constant pressure, the magnitudes of the FSC and the SSC appeared to change according to the amplitudes and durations of the FLP and the SLP. Further, the total amplitude of systole was often affected by the time of occurrence of the SSC (or the SLP). 3. Internal perfusion pressure and heart tonus were linearly related over a considerable range. With an increase in heart tonus (0–30 mg), the magnitude of the FSC was enhanced markedly in the absence of equivalent increases in the amplitude and duration of the FLP. The elevation of heart tonus was also related to an increase in beat frequency. 4. The SSC decreased in magnitude and disappeared when the beat frequency exceeded approx. 1 Hz under high perfusion pressure. Further, the abolition of the SSC resulted in a steeper slope in the curve relating beat frequency to tonus. The SSC was absent during the decline of beating caused by rapid reduction of the pressure. 5. The SSC was abolished by transverse cuts of the ganglionic trunk between the 4th and 5th large cells or between the 5th large and the 6th small cells, but the SSC often remained after the trunk was severed at the region between the 6th and 7th small cells. After severing the trunk, the heart still had the ability to respond to pressure as detected by a change of the beat frequency. 6. Spontaneous slow contractions of the cardioarterial valves were often observed.


1979 ◽  
Vol 42 (4) ◽  
pp. 975-999 ◽  
Author(s):  
K. Tazaki ◽  
I. M. Cooke

1. Semi-isolated preparations of the nine-celled cardiac ganglion of the crab, Portunus sanguinolentus, were studied electrophysiologically, using simultaneous recording from extracellular and two or three intracellular electrodes. Nine penetrations of small cells were achieved. 2. Three large (80 x 120 micron) cells lie near the anterior end of the 5-mm main trunk; two large and four small (less than 50 micron) cells at the posterior end. Large-cell axons pass along the main trunk and then exit to innervate cardiac muscle; small-cell axons do not leave the ganglion. 3. The semi-isolated ganglion produces spontaneous electrical activity organized into regularly patterned, rhythmic bursts of large- and small-cell impulses recurring at rates of 0.3-0.6/s and lasting 500-800 ms. Small impulse activity commences and ends each burst. Small cells fire trains during the burst, but impulses are not synchronized among them. Large-cell trains are synchronous, are at about one-half the frequency, and have fewer impulses than small-cell trains. 4. Intracellular recordings from small cells show a slow, pacemaker depolarization from a maximum membrane potential of -54 mV leading with only a slight inflection at ca. -50 mV to a depolarized plateau at ca. -40 mV; nonovershooting impulses are superimposed on this but cease before it repolarizes. Impulses, therefore, arise at a site distant from the soma and do not invade it. Deflections suggesting synaptic potentials are not seen. 5. Intracellular recordings from large cells show complex depolarizations corresponding to extracellularly recorded bursts. These represent excitatory postsynaptic potentials (EPSPs) corresponding with individual small-cell impulses, attenuated, non-overshooting spikes, and an underlying slow depolarization; usually no pacemaker depolarization is apparent between bursts. Chemically mediated transmission is probable for the EPSPs because they show delay, increase in amplitude with hyperpolarization, sometimes show facilitation, and are reduced in saline having one-third Ca, 3 x Mg. 6. EPSPs, impulses, and the slow depolarization occur synchronously among the large cells. Potentials recorded from posterior cells are attenuated and slower than those of the anterior cells. This is interpreted to reflect sites of occurrence more distant from the soma in the posterior than in the anterior cells. Impulses do not invade the somata. 7. Intracellular recordings from large-cell axons 4 mm from the soma show overshooting action potentials arising sharply from a base line. EPSPs are absent or highly attenuated and there is little underlying depolarization (less than 2 mV). 8. Current passing with electrodes intracellular to two cells has established directly that all large cells are electrotonically coupled and that an anterior cell and a small cell are coupled. Changes of burst rate during current passing into any large cell indicate that all large cells and small cells are electrotonically coupled. 9...


1967 ◽  
Vol 47 (2) ◽  
pp. 327-341
Author(s):  
DANIEL K. HARTLINE

1. Simultaneous recording from several pairs of electrodes placed along the ganglion and certain efferent nerves, during stimulation of other efferents, allows the course of antidromic impulses in each stimulated axon to be mapped. 2. These impulses disappear as they approach their somata, being incapable of invading them, a fact which permits identification of a particular efferent axon with a particular soma. 3. By these means the courses of all such efferent axons, and their corresponding somata, have been determined. These all belong to the five large cells. 4. The impulses from each such axon occurring during the spontaneous burst can be identified, as can impulses from each small cell. 5. Each large-cell axon appears to be inexcitable until it is a few mm from the soma. 6. If the axon branches within this inexcitable region, the branches tend to fire impulses independently. 7. The technique of cell identification opens the way to a more complete analysis of the ganglion's activity and the synaptic interactions which produce it.


1981 ◽  
Vol 94 (1) ◽  
pp. 95-104
Author(s):  
J. N. SIGGER ◽  
D. A. DORSETT

The buccal ganglia of Philine each contain a group of mechanoreceptors, consisting of 1 large and 3 small cells, with receptive fields in the oesophagus. Synaptic contacts occur between the receptors; the large cell providing an EIPSP input to its contralateral partner and to the two groups of smaller receptors. The small receptors make weak excitatory contacts with both the large receptors. The sensory cells synapse with other buccal motoneurones and interneurones, some of which show periodic activity associated with the feeding movements. Protraction phase neurones are divisible into two groups, one of which receives EPSPs from the receptors, while the other group receives IPSPs. Retraction phase neurones receive a biphasic EIPSP. The receptors provide excitatory synaptic input to a pair of interneurones which ‘gate’ the feeding cycle. A third class of neurones which are not rhythmically active during feeding receive a predominantly inhibitory EIPSP.


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