scholarly journals Red pigment concentrating hormone is a modulator of the crayfish swimmeret system

1991 ◽  
Vol 155 (1) ◽  
pp. 21-35 ◽  
Author(s):  
C. M. Sherff ◽  
B. Mulloney
Keyword(s):  
Nerve Cord ◽  
Action Potentials ◽  
Abdominal Ganglion ◽  
Red Pigment ◽  
Small Set ◽  
Bursting Activity ◽  
Phase Relationships ◽  
Nerve Cords

The crustacean red pigment concentrating hormone (RPCH) has been localized in neurons of the crayfish abdominal nerve cord and modulates the crayfish swimmeret rhythm. An antibody to RPCH labels a small set of cell bodies and axons in each abdominal ganglion. Physiological experiments in which RPCH was perfused into the ganglia of isolated nerve cords showed that RPCH modulated the swimmeret rhythm. In nerve cords that were spontaneously producing the swimmeret rhythm, RPCH lengthened both the period and the duration of bursts of action potentials, but did not alter the phase relationships between bursts in different segments. RPCH did not initiate the swimmeret rhythm in preparations that showed intermittent or no bursting activity. We believe that RPCH is released as a neurotransmitter in the lateral neuropil, where it exerts its effects on the local swimmeret circuits.

scholarly journals Synaptic transmission of nervous impulses through the last abdominal ganglion of the cockroach

1937 ◽  
Vol 122 (826) ◽  
pp. 106-118 ◽  
Keyword(s):  
Synaptic Transmission ◽  
Nerve Cord ◽  
Action Potentials ◽  
Ventral Nerve Cord ◽  
Abdominal Ganglion ◽  
Acoustic Stimuli ◽  
Excellent Opportunity ◽  
Random Activity ◽  
Previous Communication

In a previous communication (1936) we have described the response of the cereal nerve of the cricket when the cercus is subjected to acoustic stimuli. In the course of that work we attempted to trace the afferent fibres to their destination by recording from the ventral nerve cord at various levels anterior to the last abdominal ganglion. It was immediately apparent that, while some of the fibres from the acoustically sensitive end-organs of the cercus ran directly through the ganglion and up the cord, others terminated in the ganglion in synaptic relation with a relatively small number of fibres running forwards in the cord and yielding action potentials of considerable magnitude. Contrary to expectation we found that, subject to certain conditions noted below, the random activity in the abdominal nerve cord was never large enough to obscure the wanted signals, and it seemed to us that the preparation offered an excellent opportunity for an examination of the properties of a central nervous synapse. This paper describes the results of this examination.

Crawling motor patterns induced by pilocarpine in isolated larval nerve cords of Manduca sexta

1996 ◽  
Vol 76 (5) ◽  
pp. 3178-3195 ◽  
Author(s):  
R. M. Johnston ◽  
R. B. Levine
Keyword(s):  
Motor Activity ◽  
Motor Neurons ◽  
Nerve Cord ◽  
Body Wall ◽  
Motor Nerve ◽  
Rhythmic Activity ◽  
Cycle Period ◽  
Nerve Activity ◽  
Bursting Activity ◽  
Nerve Cords

1. Larval crawling is a bilaterally symmetrical behavior that involves an anterior moving wave of motor activity in the body wall muscles in conjunction with sequential movements of the abdominal prolegs and thoracic legs. The purpose of this study was to determine whether the larval CNS by itself and without phasic sensory feedback was capable of producing patterned activity associated with crawling. To establish the extent of similarity between the output of the isolated nerve cord and crawling, the motor activity produced in isolated larval nerve cords was compared with the motor activity from freely crawling larvae. 2. When exposed to the muscarinic receptor agonist pilocarpine (1.0 mM), isolated larval nerve cords produced long-lasting rhythmic activity in the motor neurons that supply the thoracic leg, abdominal body wall, and abdominal proleg muscles. The rhythmic activity evoked by pilocarpine was abolished reversibly and completely by bath application of the muscarinic-receptor antagonist atropine (0.01 mM) in conjunction with pilocarpine (1.0 mM), suggesting that the response was mediated by muscarinic-like acetylcholine receptors. 3. Similar to crawling in intact animals, the evoked activity in isolated nerve cords involved bilaterally symmetrical motor activity that progressed from the most posterior abdominal segment to the most anterior thoracic segment. The rhythmic activity in thoracic leg, abdominal proleg, and abdominal body wall motor neurons showed intrasegmental and intersegmental cycle-to-cycle coupling. The average cycle period for rhythmic activity in the isolated nerve cord was approximately 2.5 times slower than the cycle period for crawling in intact larvae, but not more variable. 4. Like crawling in intact animals, in isolated nerve cords, bursting activity in the dorsal body wall motor neurons occurred before activity in ventral/lateral body wall motor neurons within an abdominal segment. The evoked bursting activity recorded from the proleg nerve was superimposed on a high level of tonic activity. 5. In isolated nerve cords, bursts of activity in the thoracic leg levator/extensor motor neurons alternated with bursts of activity in the depressor/flexor motor neurons. The burst duration of the levator/extensor activity was brief and remained relatively steady as cycle period increased. The burst duration of the depressor/ flexor activity occupied the majority of an average cycle and increased as cycle period increased. The phase of both levator/extensor motor nerve activity and depressor/flexor motor nerve activity remained relatively stable over the entire range of cycle periods. The timing and patterning of thoracic leg motor neuron activity in isolated nerve cords quantitatively resembled thoracic leg motor activity in freely crawling larvae. 6. The rhythmic motor activity generated by an isolated larval nerve cord resembled a slower version of normal crawling in intact larvae. Because of the many similarities between activity induced in the isolated nerve cord and the muscle activity and movements of thoracic and abdominal segments during crawling, we concluded that central mechanisms can establish the timing and patterning of the crawling motor pattern and that crawling may reflect the output of a central pattern generating network.

Extracellular filaments in the perineurium of the florida lobster, Panulirus argus

1987 ◽  
Vol 45 ◽  
pp. 784-785
Author(s):  
Roy J. Baerwald ◽  
Lura C. Williamson
Keyword(s):  
Blood Brain Barrier ◽  
Glial Cells ◽  
Tannic Acid ◽  
Nerve Cord ◽  
Ventral Nerve Cord ◽  
Florida Keys ◽  
Panulirus Argus ◽  
Brain Barrier ◽  
Cacodylate Buffer ◽  
Nerve Cords

In arthropods the perineurium surrounds the neuropile, consists of modified glial cells, and is the morphological basis for the blood-brain barrier. The perineurium is surrounded by an acellular neural lamella, sometimes containing scattered collagen-like fibrils. This perineurial-neural lamellar complex is thought to occur ubiquitously throughout the arthropods. This report describes a SEM and TEM study of the sheath surrounding the ventral nerve cord of Panulirus argus.Juvenile P. argus were collected from the Florida Keys and maintained in marine aquaria. Nerve cords were fixed for TEM in Karnovsky's fixative and saturated tannic acid in 0.1 M Na-cacodylate buffer, pH = 7.4; post-fixed in 1.0% OsO4 in the same buffer; dehydrated through a graded series of ethanols; embedded in Epon-Araldite; and examined in a Philips 200 TEM. Nerve cords were fixed for SEM in a similar manner except that tannic acid was not used.

Electrical interactions between the giant axons of a polychaete worm (Sabella penicillus L.)

1980 ◽  
Vol 84 (1) ◽  
pp. 119-136
Author(s):  
D. Mellon ◽  
J. E. Treherne ◽  
N. J. Lane ◽  
J. B. Harrison ◽  
C. K. Langley
Keyword(s):  
Safety Factor ◽  
Nerve Cord ◽  
Action Potentials ◽  
Divalent Cations ◽  
Muscular Contraction ◽  
The Body ◽  
The Other ◽  
Intracellular Recordings ◽  
Giant Axons ◽  
Other Hand

Intracellular recordings demonstrated a transfer of impulses between the paired giant axons of Sabella, apparently along narrow axonal processes contained within the paired commissures which link the nerve cords in each segment of the body. This transfer appears not to be achieved by chemical transmission, as has been previously supposed. This is indicated by the spread of depolarizing and hyperpolarizing voltage changes between the giant axons, the lack of effects of changes in the concentrations of external divalent cations on impulse transmission and by the effects of hyperpolarization in reducing the amplitude of the depolarizing potential which precedes the action potentials in the follower axon. The ten-to-one attenuation of electronic potentials between the giant axons argues against the possibility of an exclusively passive spread of potential along the axonal processes which link the axons. Observation of impulse traffic within the nerve cord commissures indicates, on the other hand, that transmission is achieved by conduction of action potentials along the axonal processes which link the giant axons. At least four pairs of intact commissures are necessary for inter-axonal transmission, the overall density of current injected at multiple sites on the follower axon being, it is presumed, sufficient to overcome the reduction in safety factor imposed by the geometry of the system in the region where axonal processes join the giant axons. The segmental transmission between the giant axons ensures effective synchronization of impulse traffic initiated in any region of the body and, thus, co-ordination of muscular contraction, during rapid withdrawal responses of the worm.

Organization of the Giant Axons of the Cockroach Periplaneta Americana

1969 ◽  
Vol 50 (3) ◽  
pp. 615-627
Author(s):  
M. E. SPIRA ◽  
I. PARNAS ◽  
F. BERGMANN
Keyword(s):  
Nerve Cord ◽  
Periplaneta Americana ◽  
Thoracic Ganglion ◽  
American Cockroach ◽  
Abdominal Ganglion ◽  
Common Pathway ◽  
Average Delay ◽  
Giant Axons ◽  
Stimulation Of

1. Stimulation of the connectives between the suboesophageal and prothoracic ganglia of the American cockroach induced ipsilateral descending spikes in the abdominal giant axons with an average delay of 0·6 msec, per thoracic ganglion. 2. Nicotine at 5 µg./ml. had no effect on conduction in the abdomen but blocked ascending responses sequentially at the 6th abdominal ganglion then at the levels of T1; T2, and T3. 3. Simultaneous descending and ascending impulses resulted in mutual extinction along the nerve cord with the point of collision depending on the interval between stimuli. 4. It is suggested that a common pathway subserves ascending and descending giant impulses and models for bi-directional conduction are discussed.

Slow Activity in the Nervous System of the Earthworm, Lumbricus Terrestris

1967 ◽  
Vol 46 (3) ◽  
pp. 571-583
Author(s):  
M. B. V. ROBERTS
Keyword(s):  
Nervous System ◽  
Nerve Cord ◽  
Action Potentials ◽  
Longitudinal Muscle ◽  
Lumbricus Terrestris ◽  
Longitudinal Contraction ◽  
Peripheral Stimulation ◽  
Segmental Nerve ◽  
Slow Potentials ◽  
Slow Activity

1. Three thresholds are demonstrated in the first segmental nerve and two (sometimes three) in the second and third segmental nerves together. 2. Slow potentials recorded from the ventral nerve cord consist of several peaks. The first peak is composed of three spikes which make their appearance at different thresholds. Transmission of at least some of the slow potentials is decremental. 3. Transmission speeds in the nerve cord and segmental nerves range from 0.4 to 0.6 m./sec. 4. Action potentials in the longitudinal muscle are recorded in response to slow potentials in the nerve cord. 5. Two slow reflexes, one involving elongation, the other longitudinal contraction, are described. The latter has the lower threshold with peripheral stimulation. 6. Slow activity in the nervous system is discussed in relation to reflex activity of the earthworm and the neurone anatomy of the nerve cord and segmental nerves.

Sodium and lithium movements and axonal function in cockroach nerve cords

1975 ◽  
Vol 62 (1) ◽  
pp. 231-241
Author(s):  
RR Bennett ◽  
PB Buchan ◽  
JE Treherne
Keyword(s):  
Normal Saline ◽  
Action Potentials ◽  
Sodium Content ◽  
Significant Decline ◽  
Rapid Recovery ◽  
Sodium Ions ◽  
Bathing Medium ◽  
Sodium Regulation ◽  
Equivalent Reduction ◽  
Nerve Cords

Exposure to sodium-deficient (tris) saline caused an appreciable decline in the sodium content of intact connectives in the absence of equivalent reduction in the amplitude of the recorded action potentials. Return of sodium-depleted connectives to normal saline resulted in a rapid recovery of axonal function despite only a partial (less than 70%) recovery in sodium content. Replacement of sodium ions by those of lithium in the bathing medium resulted in a substantial accumulation of this cation. Lithium movements exhibited a marked asymetry, no significant decline in concentration being observed upon return to normal saline. These results are tentatively interpreted in terms of an exchangeable glial sodium fraction and are discussed in relation to extra-axonal sodium regulation.

Wall substructure of microtubules polymerized in vitro from tubulin of crayfish nerve cord and fixed with tannic acid

1979 ◽  
Vol 39 (1) ◽  
pp. 89-99
Author(s):  
G.B. Pierson ◽  
P.R. Burton ◽  
R.H. Himes
Keyword(s):  
Glial Cells ◽  
Tannic Acid ◽  
Nerve Cord ◽  
Associated Proteins ◽  
Nerve Cords

Microtubules of axons of crayfish nerve cord normally have 12 wall protofilaments and microtubules of surrounding glial cells have 13 protofilaments. Tubulin was isolated from such nerve cords and polymerized in vitro; tannic acid staining of sedimented microtubules showed that microtubules with 12 and 13 wall protofilaments were present, suggesting that the ability to form a microtubule with a given number of protofilaments is inherent in the tubulin or its associated proteins. The temperature of polymerization was found to influence the number of protofilaments in resultant microtubules. With assembly at 20 degrees C, for example, most of the complete microtubules had 13 protofilaments, while at 40 degrees C most showed 10 protofilaments. It is suggested that the temperature of in vitro polymerization, among other factors, can influence the angle of binding between adjacent protofilaments and thus alter the number of protofilaments required to complete the circumference of the tubule.

Coordinated Excitation of Flexor Inhibitors in the Crayfish

1980 ◽  
Vol 86 (1) ◽  
pp. 187-195
Author(s):  
CHIKAO UYAMA ◽  
TAKASHI MATSUYAMA
Keyword(s):  
Giant Axon ◽  
Experimental Results ◽  
Abdominal Ganglion ◽  
Giant Axons ◽  
The Third ◽  
Nerve Cords

In isolated abdominal nerve cords of crayfish, the medial or lateral giant axons were stimulated at a position just rostral to the first abdominal ganglion. Recordings of the impulse sequences of the flexor inhibitor (FI) were made from the anterior five ganglia, three ganglia at a time. In 20% of our preparations, one giant axon impulse caused one to four FI impulses in every abdominal third root. An equal number of FI impulses were usually produced by each abdominal ganglion for any given stimulation. The earliest FI impulse was observed at the third root of the fourth ganglion. FI impulses occurred with increasing latencies rostrally and caudally from the fourth ganglion. The FI responses to medial and lateral giant axons stimulation were essentially equivalent. FI impulses were recorded from the rostral three abdominal ganglia, while the caudal ganglia were cut off one after another from the sixth to the third ganglion. Little change was noted until after the removal of the fourth ganglion, which usually caused all FI impulses to disappear. From these experimental results, we propose a model of central mechanisms for FI excitation.

Entrainment of the Swimmeret Rhythm of the Crayfish to Controlled Movements of Some of the Appendages

1989 ◽  
Vol 144 (1) ◽  
pp. 257-278
Author(s):  
SIMON R. T. DELLER ◽  
DAVID L. MACMILLAN
Keyword(s):  
Central Pattern Generator ◽  
Small Proportion ◽  
Nerve Cord ◽  
Sensory Input ◽  
Pattern Generator ◽  
Nerve Cords

Please send reprint requests and enquiries to this author A machine was used to impose controlled movements, closely resembling natural movements, on some of the swimmerets of crayfish with their ventral nerve cords cut between thorax and abdomen. The rhythm of the unrestrained swimmerets could be entrained to the imposed frequency. Full entrainment occurred most readily when three or four swimmerets were controlled and was uncommon with two. When one was controlled, only partial entrainment was seen. A small proportion of preparations could not be entrained irrespective of the number of swimmerets controlled. Entrainment of the neural rhythm also occurred when movement was imposed on one or more swimmerets attached to an otherwise isolated nerve cord. This is the first demonstration that sensory input affects the periodicity of the swimmeret rhythm. In the light of this result, the hypothesis that swimmeret rhythm is largely controlled by a central pattern generator should be viewed with caution. It now appears that there is also an influential sensory component responsible for stabilizing and adjusting the timing of the swimmeret rhythm.

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