Neural Patterns Associated with Ventilatory Movements in Dragonfly Larvae

1970 ◽  
Vol 52 (1) ◽  
pp. 167-175
Author(s):  
P. J. MILL

1. Rhythmic bursts of motor activity associated with the expiratory phase of ventilation have been recorded from the second lateral segmental nerves of posterior abdominal ganglia in Aeshna and Anax larvae. 2. In Aeshna the rhythmic expiratory bursts contain one, or sometimes two, motor units; whereas in Anax there are almost invariably three units. In both animals only one unit is associated with action potentials in the respiratory dorso-ventral muscle. 3. Motor activity synchronized with the expiratory bursts in the second nerves has been recorded from the other lateral nerves and from the last unpaired nerve. In addition the fifth lateral nerves carry inspiratory bursts. 4. It has been confirmed that stimulation of a first segmental nerve can re-set the ventilatory rhythm by initiating an expiratory burst in the second nerves. The original frequency is immediately resumed on cessation of stimulation. 5. The nature of the ventilatory control system in dragonfly larvae is discussed in relation to other rhythmic systems in the arthropods.

1987 ◽  
Vol 62 (5) ◽  
pp. 1780-1785 ◽  
Author(s):  
M. Sibuya ◽  
I. Homma ◽  
T. Hara ◽  
N. Tsuyama

Involuntary activity of transferred intercostal motor units was examined in patients with brachial plexus injury. Since the internal intercostal nerves were detached from the thorax to reinnervate the musculus biceps brachii, it was possible to record pure intercostal motor activity in humans. Respiratory activity was seen in the latter part of the expiratory phase, thus dividing the phase into two substages (E1 and E2) by the onset of the activity. CO2 rebreathing prolonged the duration of the intercostal motor activity and increased the tidal activity as determined from the integration curve. There was a close linear correlation between these two variables. These observations indicate that expiratory activity and its duration are actively controlled in humans.


1968 ◽  
Vol 49 (2) ◽  
pp. 285-297
Author(s):  
M. BURROWS ◽  
G. A. HORRIDGE

1. Protective withdrawal of the eyecup is caused by a burst of impulses in two axons of the optic tract, one to muscles 19a, 19b and 20a, the other to muscles 18, 20b, 21 and 22. 2. At a reflex eyecup withdrawal other concurrent activity is mechanically overridden ; the tonic activity in only one muscle is inhibited centrally. At a ‘spontaneous’ withdrawal, however, all motor activity to that eyecup is inhibited. 3. The largest muscle, 19a, inactive in other eyecup movements, is the prime mover in withdrawal, and some tonic fibres of this muscle hold the eyecup withdrawn. 4. Two muscles which move the eyecup toward the mid line on optokinetic responses are excited during a withdrawal. It is therefore possible for one muscle to contribute to movements in opposite directions. 5. Repeated reflex withdrawal of an eyecup moving towards the mid line inhibits the optokinetic response of the other eye. 6. Weak stimulation of an eyecup region by a variety of means, including withdrawal, improves the optokinetic response of that eyecup and sometimes of the other eyecup


1996 ◽  
Vol 75 (5) ◽  
pp. 2005-2016 ◽  
Author(s):  
A. J. Sokoloff ◽  
T. C. Cope

1. On the basis of the orderly activation of motoneurons in a pool, one would predict that motor unit activity and whole muscle force will change at least roughly in parallel: active motor units should continue to fire as net muscle force increases and quiescent motor units should remain inactive as muscle force decreases. We have consistently observed this relationship in our studies of the medial gastrocnemius (MG) muscle, but here we report an uncoupling of the soleus muscle and some of its motor units. 2. Physiological properties and firing behaviors of 20 soleus motor units were characterized in five decerebrate cats with the use of intra-axonal stimulation and recording. Motor unit firing was elicited in reflexes initiated by muscle stretch, nerve stimulation, and mechanical stimulation of the heel. Particular emphasis was placed on the heterogenic reflexes produced in soleus by ramphold-release stretches of the MG muscle. In agreement with previous reports, either net heterogenic excitation or inhibition of the soleus muscle was produced in separate trials of MG stretch. 3. During excitation of soleus in autogenic stretch reflexes and in crossed-extension reflexes, all 20 units were recruited or increased firing, i.e., unit firing was coupled with soleus force. In the other reflexes, however, unit firing and muscle force were uncoupled for 10 of these units. Six tonically active motor units were inhibited during an increase in soleus force produced by MG stretch or by mechanical stimulation of the heel. Four motor units were activated during a decrease in soleus force produced by the same stimuli. 4. Six motor units were studied during both soleus inhibition and excitation evoked by MG stretches. One motor unit was consistently coupled to the soleus muscle response; firing increased during soleus excitation and decreased during inhibition. However, four soleus motor units were inhibited under both conditions, and one unit was excited under both conditions. Thus the firing behavior of five of these six motor units was the same in response to MG stretch, irrespective of the soleus response. 5. The uncoupling was most clearly recognized when tonically active units ceased firing during net excitation of the soleus muscle and when silent units began firing during net inhibition of the soleus muscle. Unit responses were not as striking in all trials of MG stretch (spike number increased or decreased relative to prestretch values by 1-4 spikes), but the responses were consistent across trials; in multiple stretches, spike number commonly either increased or decreased. Intertrial regularity was also observed in units for which firing was coupled with the net reflex response of the soleus muscle. 6. Divergence in the firing of soleus motor units was also observed in three cases in which records were taken simultaneously from two motor units. In one pair, one unit increased and the other decreased firing during MG stretch-evoked inhibition of soleus. In the other two pairs, one unit increased and the other decreased firing when soleus was excited by heel stimulation. In all pairs, the unit that decreased firing under these conditions had the lowest recruitment threshold in response to the soleus stretch. 7. Although all soleus motor units were classified as slow-twitch (type S), variation in their physiological properties bore some relation to firing behavior. Those units recruited during periods of soleus inhibition exhibited among the fastest conduction velocities and contraction times in our sample. In all three unit pairs sampled, the unit expressing decreases in firing had the slower conduction velocity and contraction time. 8. These findings demonstrate that soleus motor units are differentially activated and deactivated by peripheral afferents. (ABSTRACT TRUNCATED)


1986 ◽  
Vol 122 (1) ◽  
pp. 277-302
Author(s):  
M. P. Nusbaum ◽  
W. B. Kristan

Two pairs of serotonin-containing neurones, designated cells 21 and 61, were characterized physiologically and anatomically in the hirudinid leeches Macrobdella decora and Hirudo medicinalis. Both of these cells are bilaterally paired interneurones and each cell is weakly electrically coupled to the other serotonin-containing cells both intra- and interganglionically. Cells 21 and 61 are excited polysynaptically by individual identified mechano-sensory neurones. Segmental nerve shock sufficient to elicit an episode of swimming strongly excites cells 21 and 61, which then tend to generate bursts of impulses that are phase-locked to the swim motor pattern. Intracellular stimulation of either cell 21 or cell 61 often causes the initiation of swimming, acting in parallel with the nonserotonergic swim-initiator cell 204. Cells 61 and 204 are also weakly electrically coupled. The latency to swim onset by stimulating cell 21 or 61 is similar to that of cell 204 and different from that of the serotonergic Retzius cell. This result, with those in the accompanying paper (Nusbaum, 1986), suggests that unlike the Retzius cell and similar to cell 204, cells 21 and 61 synaptically contact cells of the swim central pattern generator (CPG).


1980 ◽  
Vol 210 (1181) ◽  
pp. 559-574 ◽  

When stimulated, salp chains achieve rapid coordinated changes in locomotion by the spread of epithelial action potentials or outer skin pulses (o. s. ps) from one zooid to the next along the chain. This process involves alternating epithelioneural and neuroepithelial chemical synapses. Each zooid is linked to another in the chain by two asymmetric attachment plaques; these are polarized so that transmission of o. s. ps proceeds from one zooid to the next in one direction at one plaque, and in the reverse direction at the other plaque. Sensory cells at the plaques send axons to the brain; they are not electrically coupled to the conducting epithelium in which they lie. Input from the plaque sensory cells affects the swimming generator in the brain (causing locomotor changes) and evokes synaptic activity at neuroepithelial synapses around the brain. This gives rise to o. s. ps that are conducted around the whole of the outer epithelium of the zooid and are detected at the plaques by the sensory cells of adjacent zooids. Severe stimulation of a zooid in the chain induces all zooids to separate; possible mechanisms of separation are discussed.


1974 ◽  
Vol 77 (1) ◽  
pp. 64-70 ◽  
Author(s):  
Gustav Wägar

ABSTRACT Whether the short-term regulation of thyroidal protein synthesis by TSH occurs at the transcriptional or the translational level was tested by measuring the effect of actinomycin D (act D) on the TSH-induced stimulation of L-14C-leucine incorporation into the thyroidal proteins of rats. TSH was injected 6 h before the rats were killed. The thyroid glands were then removed and incubated in vitro in the presence of L-14C-leucine for 2 h. The pronounced stimulation of leucine incorporation in the TSH-treated animals was depressed as compared with controls but still significant even when the animals had been pre-treated with 100 μg act D 24 and 7 h before sacrifice. On the other hand, act D strongly decreased incorporation of 3H-uridine into RNA. Short-term regulation of thyroidal protein synthesis by TSH appears to be partly but not wholly dependent on neosynthesis of RNA. Hence regulation may partly occur at the translation level of protein synthesis.


2008 ◽  
Author(s):  
Nichole M. Jindra ◽  
Robert J. Thomas ◽  
Douglas N. Goddard ◽  
Michelle L. Imholte

1995 ◽  
Vol 31 (8) ◽  
pp. 301-309 ◽  
Author(s):  
Govert D. Geldof

In integrated water management, the issues are often complex by nature, they are capable of subjective interpretation, are difficult to express in standards and exhibit many uncertainties. For such issues, an equilibrium approach is not appropriate. A non-equilibrium approach has to be applied. This implies that the processes to which the integrated issue pertains, are regarded as “alive”’. Instead of applying a control system as the model for tackling the issue, a network is used as the model. In this network, several “agents”’ are involved in the modification, revision and rearrangement of structures. It is therefore an on-going renewal process (perpetual novelty). In the planning process for the development of a groundwater policy for the municipality of Amsterdam, a non-equilibrium approach was adopted. In order to do justice to the integrated character of groundwater management, an approach was taken, containing the following features: (1) working from global to detailed, (2) taking account of the history of the system, (3) giving attention to communication, (4) building flexibility into the establishing of standards, and (5) combining reason and emotions. A middle course was sought, between static, rigid but reliable on the one hand; dynamic, flexible but vague on the other hand.


1993 ◽  
Vol 289 (1) ◽  
pp. 117-124 ◽  
Author(s):  
S Roche ◽  
J P Bali ◽  
R Magous

The mechanism whereby gastrin-type receptor and muscarinic M3-type receptor regulate free intracellular Ca2+ concentration ([Ca2+]i) was studied in rabbit gastric parietal cells stimulated by either gastrin or carbachol. Both agonists induced a biphasic [Ca2+]i response: a transient [Ca2+]i rise, followed by a sustained steady state depending on extracellular Ca2+. Gastrin and carbachol also caused a rapid and transient increase in Mn2+ influx (a tracer for bivalent-cation entry). Pre-stimulation of cells with one agonist drastically decreased both [Ca2+]i increase and Mn2+ influx induced by the other. Neither diltiazem nor pertussistoxin treatment had any effect on agonist-stimulated Mn2+ entry. Thapsigargin, a Ca(2+)-pump inhibitor, induced a biphasic [Ca2+]i increase, and enhanced the rate of Mn2+ entry. Preincubation of cells with thapsigargin inhibits the [Ca2+]i increase as well as Mn2+ entry stimulated by gastrin or by carbachol. Thapsigargin induced a weak but significant increase in Ins(1,4,5)P3 content, but this agent had no effect on the agonist-evoked Ins(1,4,5)P3 response. In permeabilized parietal cells, Ins(1,4,5)P3 and caffeine caused an immediate Ca2+ release from intracellular pools, followed by a reloading of Ca2+ pools which can be prevented in the presence of thapsigargin. We conclude that (i) gastrin and carbachol mobilize common Ca2+ intracellular stores, (ii) Ca2+ permeability secondary to receptor activation involves neither a voltage-sensitive Ca2+ channel nor a GTP-binding protein from the G1 family, and (iii) agonists regulate common Ca2+ channels in depleting intracellular Ca2+ stores.


1984 ◽  
Vol 62 (1) ◽  
pp. 153-156 ◽  
Author(s):  
Archana Chaudhry ◽  
John W. Downie ◽  
Thomas D. White

The present study was carried out to assess the possible role of ATP in the noncholinergic, nonadrenergic transmission in the rabbit urinary bladder. When rabbit detrusor muscle strips were superfused with medium containing firefly luciferin–luciferase and stimulated transmurally at low stimulation parameters, tetrodotoxin-sensitive contractions were obtained but no release of ATP could be detected. However, at somewhat higher stimulation parameters, release of ATP was observed. This release of ATP was not diminished by tetrodotoxin indicating that ATP was not likely released as a result of propagated action potentials in nerves. Because contractions persisted in the presence of tetrodotoxin, it is possible that the ATP might have been released as a result of direct electrical stimulation of the muscle. These results do not support the idea that ATP is released as a neurotransmitter in the rabbit bladder.


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