scholarly journals Functional Organization of the Cardiac Ganglion of the Lobster, Homarus americanus

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.

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.


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 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.


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...


1969 ◽  
Vol 50 (2) ◽  
pp. 275-295 ◽  
Author(s):  
JOHN A. CONNOR

1. The patterned burst activity of cardiac pacemaker ganglion cells in Homarus americanus has been studied by means of intracellular recording electrodes. 2. Burst activity, highly similar to that seen in cells of intact ganglia, has been demonstrated in ganglion sections containing as few as two large-cell bodies. 3. Studies of the sectioned preparations have shown that potential deflexions during the burst period are mainly endogenous activity of the respective cells and not post-synaptic potentials. 4. The behaviour of the cells in the period between bursts suggests the action of an inhibitory conductance change in each of the cells during this period.


1962 ◽  
Vol 40 (1) ◽  
pp. 7-12
Author(s):  
J. M. Langlois ◽  
Guy Lamarche

The projections of the trigeminal nerve in the pontine reticular formation of the cat have been investigated by recording unit activity, after physiological stimulation of the face, in 30 "encéphales isolés" preparations. No somatotopical arrangement was found but a high degree of spatial convergence onto pontine reticular units exists and a certain degree of functional organization was observed.


1993 ◽  
Vol 177 (1) ◽  
pp. 149-167 ◽  
Author(s):  
J. R. Trimarchi ◽  
A. M. Schneiderman

Cinematographic analysis reveals that an important component of the light-elicited escape response of Drosophila melanogaster is the extension of the femur-tibia joint of the mesothoracic leg. During the jumping phase of the response, this extension works synergistically with extension of the femur. Femur extension is generated by contraction of the tergotrochanteral muscle (TTM), one of four previously described escape response muscles. Femur-tibia joint extension in the mesothoracic leg has been thought to be controlled by contraction of the tibial levator (TLM), an intrinsic leg muscle. We investigated the activation of the TLM during the escape response. Electrical stimulation of the giant fiber interneuron that mediates the escape response results in activation of the TLM with a latency of 1.46 +/− 0.02 ms. The TLM is innervated by a motor neuron (TLMn) with a large cell body in the mesothoracic ganglion. The TLMn has extensive arborizations in the lateral mesothoracic leg neuromere and has a prominent medially directed neurite. To investigate possible presynaptic inputs activating the TLMn during the escape response, we analyzed the muscle responses of two mutants, giant fiber A1 and bendless. Our analysis suggests that the TLMn is activated by a novel pathway.


1995 ◽  
Vol 73 (6) ◽  
pp. 2578-2583 ◽  
Author(s):  
C. A. Pratt

1. The functional organization of heterogenic reflexes produced by activation of extensor force receptors (Golgi tendon organs) was studied in intact cats during stationary stance. Intramuscular stimulation (200 Hz, 20 ms) of hindlimb extensor muscles via chronically implanted electrodes was used to evoke weak muscle contractions and naturally activate Golgi tendon organ Ib afferents while cats stood unrestrained with each paw on a moveable triaxial force plate. 2. Intramuscular stimulation of every hindlimb extensor muscle tested in this study evoked excitatory responses that were widely distributed among hindlimb extensor muscles. Source and target specializations in the functional organization of this positive force feedback system were also observed. For example, stimulation of ankle extensors typically excited extensors and flexors at the ankle and hip (but not knee), whereas stimulation of hip extensors typically excited only extensors at all three joints. In addition, intramuscular stimulation of either lateral (LG) or medial (MG) gastrocnemius consistently inhibited soleus while exciting other extensors at the ankle and more proximal joints. 3. The electromyographic (EMG) reflex responses described above are attributed to the natural (via muscle contraction) activation of extensor group Ib afferents. Direct activation of intramuscular afferents by the stimulus was unlikely because there was no evidence that Ia afferents, which have the lowest electrical thresholds, were activated. Both the observed inhibition of the synergist, soleus, and the excitation of the antagonist, tibialis anterior, produced by gastrocnemius stimulation are opposite to the reflex effects that would be produced at the ankle by activation of gastrocnemius Ia afferents.(ABSTRACT TRUNCATED AT 250 WORDS)


1972 ◽  
Vol 56 (3) ◽  
pp. 621-637
Author(s):  
MICHAEL S. BERRY

1. The buccal ganglia of Planorbis contain a population of electrically coupled small cells. This has been studied, in preparations of isolated ganglia, by recording intracellularly from the cells two at a time. 2. The population is usually silent but activity initiated in any one of its members tends to spread to the rest of the population in both ganglia. Failure of spread, or fatigue, gradually occurs on repetition. 3. The group has the properties of a trigger system, initiating prolonged patterned activity in large numbers of neurones in the buccal ganglia. This may normally initiate feeding. 4. In addition to central processes, both in the buccal ganglia and to the rest of the CNS, the system has peripheral axons in most of the buccal nerves. No synaptic input could be demonstrated. 5. Action potentials in some of the cells increase greatly in duration with repetition. The resulting electrotonic EPSP's, recorded in closely coupled trigger cells, correspondingly increase in size. The possible integrative significance of this is discussed, especially its effect in offsetting fatigue. 6. In some preparations spontaneous bursting occurred in trigger cells and this elicited burst activity in large neurones, including motoneurones. The system may have an intrinsic pacemaker.


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