Motor neurons of grasshopper metathoracic ganglion occur in stereotypic anatomical groups

1990 ◽  
Vol 297 (2) ◽  
pp. 298-312 ◽  
Author(s):  
Melody V. S. Siegler ◽  
Cynthia A. Pousman
Keyword(s):  
Motor Neurons ◽  
Metathoracic Ganglion

Serotonergic modulation of locust motor neurons

1995 ◽  
Vol 73 (3) ◽  
pp. 923-932 ◽  
Author(s):  
D. Parker
Keyword(s):  
Cyclic Amp ◽  
Motor Neurons ◽  
Schistocerca Gregaria ◽  
Phosphodiesterase Inhibitor ◽  
Membrane Resistance ◽  
Excitatory Postsynaptic Potential ◽  
Metathoracic Ganglion ◽  
Bath Application ◽  
Potassium Conductances ◽  
5 Ht Uptake

1. The effects of the putative endogenous neuromodulator serotonin (5-HT) on the fast extensor and flexor tibiae motor neurons in the locust (Schistocerca gregaria) metathoracic ganglion, were analyzed. 2. 5-HT consistently increased the duration of the fast extensor spike and usually reduced the afterhyperpolarization, although this effect was less consistent. The spike broadening in the fast extensor was associated with an increase in the amplitude of the excitatory postsynaptic potential (EPSP) evoked monosynaptically in the flexor motor neurons by fast extensor stimulation. 5-HT also increased the membrane resistance of the fast extensor and flexor tibiae motor neurons. 3. The effects of 5-HT were mimicked by bath application of the 5-HT uptake inhibitor imipramine, and blocked by the 5-HT receptor antagonist ketanserin. The effects were also mimicked by dibutryl cyclic AMP, a membrane permeant analogue of cyclic AMP, and by the phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine, but not by dibutryl cyclic GMP. The 5-HT-dependent modulation was blocked by the protein kinase A inhibitor H8. In addition, injection of cyclic AMP into the fast extensor or a flexor motor neuron could mimic the effects of 5-HT on these neurons. 4. 5-HT probably broadened the FETi action potential by modulating potassium conductances responsible for spike repolarization. 5. These results show that 5-HT modulates both the fast extensor and flexor tibiae motor neurons, resulting in potentiation of synaptic transmission between these neurons. In addition, the increase in flexor membrane resistance will potentiate other inputs onto these cells, which will affect the output of the motor neurons during locomotion.

Innervation pattern of a pool of nine excitatory motor neurons in the flexor tibiae muscle of a locust hind leg

1998 ◽  
Vol 201 (12) ◽  
pp. 1885-1893 ◽  
Author(s):  
K Sasaki ◽  
M Burrows
Keyword(s):  
Motor Neurons ◽  
Muscle Fibres ◽  
Main Body ◽  
Intracellular Recordings ◽  
Innervation Pattern ◽  
Flexor Muscle ◽  
Fibre Bundles ◽  
Metathoracic Ganglion ◽  
Overlapping Sets ◽  
Individual Motor

The flexor tibiae muscle of a locust hind leg consists of 10-11 pairs of fibre bundles in the main body of the muscle and a distal pair of bundles that form the accessory flexor muscle, all of which insert onto a common tendon. It is much smaller than the antagonistic extensor tibiae muscle and yet it is innervated by nine excitatory motor neurons, compared with only two for the extensor. To determine the pattern of innervation within the muscle by individual motor neurons, branches of the nerve (N5B2) that supplies the different muscle bundles were backfilled to reveal somata in the metathoracic ganglion. This showed that different muscle bundles are innervated by different numbers of excitatory motor neurons. Physiological mapping of the innervation was then carried out by intracellular recordings from the somata of flexor motor neurons in the metathoracic ganglion using microelectrodes. Spikes were evoked in these neurons by the injection of current, and matching junctional potentials were sought in fibres throughout the muscle using a second intracellular electrode. Each motor neuron innervates only a restricted array of muscle fibres and, although some innervate a larger array than others, none innervates fibres throughout the muscle. Some motor neurons innervate only proximal fibres and others only more distal fibres, so that the most proximal and most distal bundles of muscle fibres are innervated by non-overlapping sets of motor neurons. More motor neurons innervate proximal bundles than distal ones, and there are some asymmetries in the number of motor neurons innervating corresponding bundles on either side of the tendon. Individual motor neurons cause slow, fast or intermediate movements of the tibia, but their patterns of innervation overlap in the different muscle bundles. Furthermore, individual muscle fibres may also be innervated by motor neurons with different properties.

Rhythmic patterns evoked in locust leg motor neurons by the muscarinic agonist pilocarpine

1993 ◽  
Vol 69 (5) ◽  
pp. 1583-1595 ◽  
Author(s):  
S. Ryckebusch ◽  
G. Laurent
Keyword(s):  
Motor Neurons ◽  
Rhythmic Activity ◽  
Cycle Period ◽  
Muscarinic Agonist ◽  
Strongly Coupled ◽  
Weakly Coupled ◽  
Metathoracic Ganglion ◽  
Common Drive ◽  
Muscarinic Cholinergic

1. When an isolated metathoracic ganglion of the locust was superfused with the muscarinic cholinergic agonist pilocarpine, rhythmic activity was induced in leg motor neurons. The frequency of this induced rhythm increased approximately linearly from 0 to 0.2 Hz with concentrations of pilocarpine from 10(-5) to 10(-4) M. Rhythmic activity evoked by pilocarpine could be completely and reversibly blocked by 3 x 10(-5) M atropine, but was unaffected by 10(-4) M d-tubocurarine. 2. For each hemiganglion, the observed rhythm was characterized by two main phases: a levator phase, during which the anterior coxal rotator, levators of the trochanter, flexors of the tibia, and common inhibitory motor neurons were active; and a depressor phase, during which depressors of the trochanter, extensors of the tibia, and depressors of the tarsus were active. Activity in depressors of the trochanter followed the activity of the levators of the trochanter with a short, constant interburst latency. Activity in the levator of the tarsus spanned both phases. 3. The levator phase was short compared with the period (0.5-2 s, or 10-20% of the period) and did not depend on the period. The interval between the end of a levator burst and the beginning of the following one thus increased with cycle period. The depressor phase was more variable, and was usually shorter than the interval between successive levator bursts. 4. Motor neurons in a same pool often received common discrete synaptic potentials (e.g., levators of trochanter or extensors of tibia), suggesting common drive during the rhythm. Coactive motor neurons on opposite sides (such as left trochanteral depressors and right trochanteral levators), however, did not share obvious common postsynaptic potentials. Depolarization of a pool of motor neurons during its phase of activity was generally accompanied by hyperpolarization of its antagonist(s) on the same side. 5. Rhythmic activity was generally evoked in both hemiganglia of the metathoracic ganglion, but the intrinsic frequencies of the rhythms on the left and right were usually different. The activity of the levators of the trochanter on one side, however, was strongly coupled to that of the depressors of the trochanter on the other side. 6. The locomotory rhythm was weakly coupled to the ventilatory rhythm such that trochanteral levator activity on either side never occurred during the phase of spiracle opener activity corresponding to inspiration. 7. The rhythmic activity observed in vitro bears many similarities to patterns of neural and myographic activity recorded during walking. The similarities and differences are discussed.

scholarly journals GABA-like immunoreactivity in nonspiking interneurons of the locust metathoracic ganglion

2002 ◽  
Vol 205 (23) ◽  
pp. 3651-3659 ◽  
Author(s):  
M. Wildman ◽  
S. R. Ott ◽  
M. Burrows
Keyword(s):  
Membrane Potential ◽  
Motor Neurons ◽  
Lucifer Yellow ◽  
Current Injection ◽  
Aminobutyric Acid ◽  
Homogeneous Population ◽  
Metathoracic Ganglion ◽  
Nonspiking Interneurons ◽  
Intracellular Microelectrodes ◽  
Gaba Immunohistochemistry

SUMMARYNonspiking interneurons are important components of the premotor circuitry in the thoracic ganglia of insects. Their action on postsynaptic neurons appears to be predominantly inhibitory, but it is not known which transmitter(s) they use. Here, we demonstrate that many but not all nonspiking local interneurons in the locust metathoracic ganglion are immunopositive for GABA (γ-aminobutyric acid). Interneurons were impaled with intracellular microelectrodes and were shown physiologically to be nonspiking. They were further characterized by defining their effects on known leg motor neurons when their membrane potential was manipulated by current injection. Lucifer Yellow was then injected into these interneurons to reveal their cell bodies and the morphology of their branches. Some could be recognised as individuals by comparison with previous detailed descriptions. Ganglia were then processed for GABA immunohistochemistry. Fifteen of the 17 nonspiking interneurons studied were immunopositive for GABA, but two were not. The results suggest that the majority of these interneurons might exert their well-characterized effects on other neurons through the release of GABA but that some appear to use a transmitter other than GABA. These nonspiking interneurons are therefore not an homogeneous population with regard to their putative transmitter.

Coupling of Efferent Neuromodulatory Neurons to Rhythmical Leg Motor Activity in the Locust

1998 ◽  
Vol 79 (1) ◽  
pp. 361-370 ◽  
Author(s):  
Sylvie Baudoux ◽  
Carsten Duch ◽  
Oliver T. Morris
Keyword(s):  
Motor Activity ◽  
Motor Neurons ◽  
Spike Activity ◽  
Motor Pattern ◽  
Rhythmic Activity ◽  
Motor Output ◽  
Variable Activity ◽  
Metathoracic Ganglion ◽  
Dum Neurons ◽  
Dorsal Unpaired Median

Baudoux, Sylvie, Carsten Duch, and Oliver T. Morris. Coupling of efferent neuromodulatory neurons to rhythmical leg motor activity in the locust. J. Neurophysiol. 79: 361–370, 1998. The spike activity of neuromodulatory dorsal unpaired median (DUM) neurons was analyzed during a pilocarpine-induced motor pattern in the locust. Paired intracellular recordings were made from these octopaminergic neurons during rhythmic activity in hindleg motor neurons evoked by applying pilocarpine to an isolated metathoracic ganglion. This motor pattern is characterized by two alternating phases: a levator phase, during which levator, flexor, and common inhibitor motor neurons spike, and a depressor phase, during which depressor and extensor motor neurons spike. Three different subpopulations of efferent DUM neurons could be distinguished during this rhythmical motor pattern according to their characteristic spike output. DUM 1 neurons, which in the intact animal do not innervate muscles involved in leg movements, showed no change apart from a general increase in spike frequency. DUM 3 and DUM 3,4 neurons produced the most variable activity but received frequent and sometimes pronounced hyperpolarizations that were often common to both recorded neurons. DUM 5 and DUM 3,4,5 neurons innervate muscles of the hindleg and showed rhythmical excitation leading to bursts of spikes during rhythmic activity of the motor neurons, which innervate these same muscles. Sometimes the motor output was coordinated across both sides of the ganglion so that there was alternating activity between levators of both sides. In these cases, the spikes of DUM 5 and DUM 3,4,5 neurons and the hyperpolarization of DUM 3 and DUM 3,4 neurons occurred at particular phases in the motor pattern. Our data demonstrate a central coupling of specific types of DUM neurons to a rhythmical motor pattern. Changes in the spike output of these particular efferent DUM neurons parallel changes in the motor output. The spike activity of DUM neurons thus may be controlled by the same circuits that determine the action of the motor neurons. Functional implications for real walking are discussed.

Action of locust neuromodulatory neurons is coupled to specific motor patterns

1995 ◽  
Vol 74 (1) ◽  
pp. 347-357 ◽  
Author(s):  
M. Burrows ◽  
H. J. Pfluger
Keyword(s):  
Motor Neurons ◽  
Motor Pattern ◽  
Intracellular Recordings ◽  
Flexor Muscle ◽  
Motor Patterns ◽  
Specific Subset ◽  
Metathoracic Ganglion ◽  
Flexor Muscles ◽  
Dum Neurons ◽  
Dorsal Unpaired Median

1. Many muscles of the locust are supplied by dorsal unpaired median neurons (DUM neurons) that release octopamine and alter the contractions caused by spikes in motor neurons. To determine when these neuromodulatory neurons are normally activated during behaviour, intracellular recordings were made simultaneously from them and from identified motor neurons during the specific motor pattern that underlies kicking. A kick consists of a rapid and powerful extension of the tibia of one or both hind legs that is produced by a defined motor pattern. Only 3 identified DUM neurons of the 20 in the metathoracic ganglion spike during a kick, and they supply muscles involved in generating the kick. Their spikes occur in a distinctive and repeatable pattern that is closely linked to the pattern of spikes in the flexor and extensor tibiae motor neurons. When the extensor and flexor muscles cocontract, these three DUM neurons produce a burst of spikes at frequencies that can rise to 25 Hz, and with the number of spikes (3-15) related to the duration of this phase of the motor pattern. The spikes stop when the flexor muscle is inhibited and therefore before the tibia is extended rapidly. The other DUM neurons which supply muscles that are not directly involved in kicking are either inhibited or spike only sporadically. 2. The activation of a specific subset of DUM neurons during kicking may thus be timed to influence the action of the muscles that participate in this movement and appear to be controlled by the same circuits that determine the actions of the participating motor neurons. These modulatory neurons thus have specific individual actions in the control of movement.

The processing of mechanosensory information by spiking local interneurons in the locust

1985 ◽  
Vol 54 (3) ◽  
pp. 463-478 ◽  
Author(s):  
M. Burrows
Keyword(s):  
Motor Neurons ◽  
Receptive Fields ◽  
The Body ◽  
Direct Stimulation ◽  
Response Characteristics ◽  
Local Interneurons ◽  
Metathoracic Ganglion ◽  
Different Response ◽  
Individual Motor ◽  
Stimulation Of

The responses and receptive fields of a group of spiking local interneurons in the metathoracic ganglion of the locust were defined by making intracellular recordings from them while moving joints of a hindleg and stimulating external mechanoreceptors. Some interneurons respond both to inputs from internal mechanoreceptors (proprioceptors) at particular joints and to inputs from an array of external mechanoreceptors. The effects of both types of receptor can be excitatory or inhibitory. Other interneurons respond to proprioceptive input alone. There is a spectrum of responses. At one extreme are interneurons that respond tonically, the frequency of their spikes being determined by the angle of a particular joint. At the other extreme are interneurons that respond phasically to imposed movements of a joint in any direction. Inbetween are interneurons that respond with either a rapidly or a more slowly adapting change in the frequency of their spikes to the displacement of a joint in only one direction. Each movement of a particular joint excites or inhibits several interneurons with a range of different response characteristics. An interneuron typically receives inputs from only one joint, though some are excited by both femoral and tibial receptors. The interneurons spike during active movements of a leg elicited by direct stimulation of individual motor neurons, and during movements elicited by tactile stimulation of other parts of the body.

Cooperative Mechanisms Between Leg Joints of Carausius morosusII. Motor Neuron Activity and Influence of ConditionalBursting Interneuron

1998 ◽  
Vol 79 (6) ◽  
pp. 2977-2985 ◽  
Author(s):  
Dennis E. Brunn ◽  
Antje Heuer
Keyword(s):  
Motor Neuron ◽  
Motor Neurons ◽  
Lucifer Yellow ◽  
Companion Paper ◽  
Stick Insect ◽  
Neuron Activity ◽  
Local Interneuron ◽  
Metathoracic Ganglion ◽  
Thoracic Part ◽  
Swing Movement

Brunn, Dennis E. and Antje Heuer. Cooperative mechanisms between leg joints of Carausius morosus. II. Motor neuron activity and influence of conditional bursting interneuron. J. Neurophysiol. 79: 2977–2985, 1998. The activity of the motor neuron pools of the protractor coxae muscle and of the thoracic part of the depressor trochanteris muscle during forward walking in the stick insect was investigated, and a spiking local interneuron, able to produce “endogenous bursting” and innervating both motor neuron pools, was identified. Extracellular recordings of the motor neurons innervating the protractor and the thoracic depressor of front, middle, and rear legs, respectively, were made with oil-hook electrodes from the peripheral nerves nl2c and nl4a while the animals were walking on a styrofoam treadwheel. The corresponding leg movements were registered and phase histograms were created with the software Spike2. Intracellular recordings were made in the neuropile of the metathoracic ganglion with glass electrodes filled with the dye Lucifer yellow. In all three legs measured (front, middle, and rear), both motor neuron pools increased their activity during the swing movement. The increase in the activity of the protractor motor neurons started at the end of the stance ∼100 ms before reaching the posterior extreme position (PEP), and the activity of the large-sized depressor motor neurons increased as soon as the tarsus was lifted at the PEP. A local spiking interneuron was identified that excited both motor neuron pools. In 4 of 23 recordings the interneuron started to burst in synchrony with protractor and thoracic depressor motor neurons. During bursting a depolarizing stimulus reinforced and a hyperpolarizing stimulus inhibited the activity of both motor neuron pools. Thus we conclude that the thoracic part of the depressor trochanteris muscle might be a component of the neuromuscular system that shapes the swing movement. The two proximal joints, subcoxal and coxa-trochanter, connected mechanically via the thoracic part of the depressor trochanteris muscle, are also connected neurally by segmental and intersegmental spiking interneurons (this paper) and by nonspiking local interneurons (see companion paper).

Interactions between segmental leg central pattern generators during fictive rhythms in the locust

1994 ◽  
Vol 72 (6) ◽  
pp. 2771-2785 ◽  
Author(s):  
S. Ryckebusch ◽  
G. Laurent
Keyword(s):  
Motor Neuron ◽  
Motor Neurons ◽  
Central Pattern Generators ◽  
Rhythmic Activity ◽  
Legged Locomotion ◽  
Adjacent Segment ◽  
Muscarinic Agonist ◽  
Thoracic Ganglia ◽  
Metathoracic Ganglion ◽  
Phase Relationships

1. Rhythmic activity of leg motor neurons could be evoked in isolated locust thoracic ganglia as well as in preparations of two or three connected thoracic ganglia superfused with the muscarinic agonist pilocarpine. Rhythms were always more regular and reliably elicited in single isolated ganglia. When the ganglia were connected, rhythmic activity of leg motor neurons was not usually simultaneously evoked in all six hemiganglia. Typically, some of the hemiganglia were rhythmically active, whereas others showed tonic or highly irregular activity. 2. Action potentials from leg motor neuron pools were recorded extracellularly from motor nerves and cross-correlated with the use of standard algorithms. The following correlations were observed between activities of motor neurons in different hemisegments. 1) Within a segment, trochanteral levators were coactive with contralateral trochanteral depressors. This correlation was strong in the metathoracic ganglion, and weaker in the pro- and mesothoracic ganglia. 2) Coupling between levators on opposite sides of the same segment was variable in the pro- and mesothoracic ganglia, because phase relationships between levators were different in each preparation and could also change during the course of an experiment. In the metathoracic ganglion, levators on opposite sides were never coactive. 3) Trochanteral levators were often active within a short latency of levator bursts in an ipsilateral adjacent hemiganglion. In addition, levators in one segment were often inhibited during levators bursts in the ipsilateral adjacent segment. 4) Trochanteral levators were strongly coupled to ipsilateral adjacent trochanteral depressors, for all three thoracic ganglia. 3. The phase relationships between motor neuron activities revealed by cross-correlation are discussed in the context of what is known about the mechanisms involved in the control of intersegmental coupling during legged locomotion.

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