Ion-channel block in insect muscle fibre membrane by the venom of the digger wasp, Philanthus triangulum F.

External miniature postsynaptic potentials were recorded from fibres of the metathoracic retractor unguis muscle of Schistocerca gregaria. At concentrations from 0.4 to 0.5 bee units/ml the venom of European Philanthus triangulum causes a decrease in amplitude and in half-decay time of miniature potentials. It is suggested that the venom, partially blocks the current by shortening the ion-channel open-life-time in the postsynaptic membrane.     

Effects of the venom of the solitary wasp Philanthus triangulum F. on glutamate uptake in the nerve endings of locust muscles—A high resolution autoradiographic study

Using electron microscope autoradiography it was shown that the glutamate uptake in both glia cells and axon in the synaptic region of locust muscles was reduced to ca. 50% under the influence of the venom of the solitary wasp Philanthus triangulum F. However, the ratio of the glutamate accumulation in the glia and the nerves remained identical. Implications are discussed in relation to known postsynaptic effects of the venom of Philanthus triangulum F.     

Further pharmacological study on the cholinergic and glutaminergic properties of the radula muscles of a mollusc,Rapana thomasiana

1. In the radula protractor of the prosobranch mollusc Rapana thomasiana, both twitch contractions and acetylcholine contractions were markedly depressed or blocked by propantheline (10⁻⁵ M) and strychnine (10⁻⁵ M), but in the radula retractor, only acetylcholine contraction was markedly affected by the antagonists,2. Glutamate contractions of both of the muscles were little or slightly affected by the drugs.3. Twitch contraction of the protractor was slowly depressed when the muscle was immersed in concanavalin A (0.3 mg/ml), while that of the retractor was first potentiated and then slowly depressed in it.4. In both of the muscles, glutamate contractions were markedly enhanced by the lectin, but acetylcholine contractions were not affected.5. These results support the notion that the principal excitatory neurotransmitter in the protractor is acetylcholine, whereas that in the retractor is glutamate.     

Alcohol-induced potentiation of the neurally evoked contractions of the retractor unguis muscle of the locust, Schistocerca gregaria

Each of a series of seven monohydroxyl alcohols caused an increase in the force of the neurally evoked contractions of the innervated retractor unguis muscle isolated from the metathoracic femurs of the locust, Schistocerca gregaria. The negative logarithm of equipotent concentrations of the alcohols was proportional to the logarithm of the partition coefficient (1-octanol/water) of the alcohols: $\text{log}\text{1}\text{C}\text{= 1·282}\text{log}\text{P+1·684}$, where C is concentration, and P is the partition coefficient.Ethylene glycol and glycerol did not potentiate the contractions, possibly due to their very low lipophilic character. Acetone (10^?2 M) and benzene (10^?5 M) also potentiated the neurally evoked contractions of the insect muscle.     

β-philanthotoxin,a novel glutamatergic antagonist for insect neuromuscular transmission

1. The molecular structure of β-philanthotoxin (β-PTX), a toxin from the insect paralysing venom of the wasp Philanthus triangulum, has been elucidated using NMR and mass spectrometry. β-PTX has a polyamine character: C₅H₁₁·NH·CO·(CH₂)₄·NH·(CH₂)₃·NH₂. This structure has been confirmed by synthesis.2. In the locust muscle fibre β-PTX blocks iontophoretically evoked glutamate potentials in a non-activation induced manner. β-PTX also blocks the nicotinic transmission in the insect CNS, however, at much higher toxin concentrations.3. β-PTX reduces the frequency of postsynaptic channel opening and reduces the duration of open times.4. These results suggest an effect of β-PTX on kinetics of glutamate activated ion channels, different from acting as an open channel blocker.     

Cerebral motoneurons mediating tentacle retraction in the land slug Ariolimax columbianus

(1) Tentacle retraction in the land slug Ariolimax columbianus can be elicited by stimulation of all nerves and connectives of the ipsi- and contralateral cerebral ganglia. (2) Six neurons in the left cerebral ganglion were classified as tentacle retraction motoneurons because their action potentials are followed one-for-one with constant delay by action potentials in the left tentacle retractor nerve and their depolarization causes retraction of the ipsilateral tentacle. The motoneurons can be identified by size, pattern of pigmentation, position, and physiological characteristics. (3) Each retractor motoneuron discharges at a rather constant rate and has more than one source of excitatory input, but no IPSPs were observed. No synaptic connections between the six retractor motoneurons were found. The nerve action potentials that correspond to each motoneurons are distinguishable by waveform and size rank. (4) Each motoneuron elicits visible contractions in a particular region of the ipsilateral retractor muscle, but the motor fields of some motoneurons overlap. Some motoneurons mediate relatively rapid contractions while others cause slower responses. (5) There is one-for-one correspondence between action potentials of the largest unit recorded extracellularly in the retractor nerve and exciatory junction potentials recorded from the retractor muscle. No evidence of a peripheral neural plexus was found in serial sections of the retractor muscle.     

Slowly-reversible block of glutamate receptor-channels by venoms of the spiders, Argiope trifasciata and Araneus gemma

Venom from two species of spider has been tested on the locust glutamatergic nerve-muscle system. The neurally-evoked twitch contraction of locust metathoracic retractor unguis muscle was abolished in the presence of venom and only slowly recovered following its removal. The twitch inhibition onset rate was venom concentration and stimulation frequency dependent. The mechanical response of this muscle to L-glutamate was also inhibited by spider venom. Complete abolition of the potential evoked by ionophoresis of L-glutamate to excitatory junctions on locust metathoracic extensor tibiae muscle was obtained with low concentrations of venom and recovery on washing was either slow and incomplete or not evident. The ionophoretic studies and twitch contraction studies indicate that the venom acts only when the glutamate receptor channel complex is activated by agonist. This conclusion is supported by data of the effects of venom on the voltage clamped excitatory postsynaptic current recorded from locust extensor tibiae muscle. Preliminary attempts to identify and isolate the active principles in these spider venoms indicate that activity is restricted to a molecule(s) of low (less than 1000 dalton's) molecular weight.     

Myogenic contractions in locust muscle induced by proctolin and by wasp, Philanthus triangulum, venom

Apparently myogenic slow contractions of the extensor tibiae of Locusta migratoria can be induced by proctolin in a concentration of 10^?10 to 10^?9 mole per liter perfusion fluid. Proctolin in a concentration of 10^?8 mole/l causes a prolonged contraction interrupted by rhythmical relaxations. Higher concentrations of proctolin cause a powerful but irreversible contraction.In some preparations in which proctolin is ineffective in a concentration of 10^?9 mole/l, a short stimulation of nerve 3b can initiate a series of rhythmic contractions. If, however, nerve 3b is stimulated at the peak of such a contraction a rapid relaxation is induced.Administration of the venom of Philanthus triangulum in a concentration which blocks the excitatory and inhibitory neuromuscular transmission, induces similar myogenic contractions. Stimulation of nerve 3b at the peak of such a contraction again causes a relaxation. Similar myogenic contractions can also be induced by administration of a homogenate of a locust.     

Neuromuscular junctions and L-glutamate-sensitive sites in the fleshfly, Sarcophaga bullata.

Sites have been located on retractor unguis and trochantal depressor muscle fibres of Sarcophaga which respond to iontophoretic application of l-glutamate. No such sites could be found on flight muscle fibres. Ultrastructural examination of the three muscles reveals differences between the muscles in the positions of the neuromuscular junctions. A correlation can be made between the sites of the neuromuscular junctions and the iontophoretically sensitive sites. The possibility of l-glutamate fulfilling a transmitter rôle in these muscles is discussed.     

The mode of action of phenylhydrazine hydrochloride on the locust neuromuscular system

The action of the carbonyl reagent phenylhydrazine hydrochloride (Phen. HCl) on locust excitatory neuromuscular systems was studied by examining the effects of this compound on the mechanical and electrical properties of the retractor unguis and extensor tibiae muscles of the locust Schistocerca gregaria.Low concentrations of Phen. HCl (10^?9 w/v to 2·5 × 10^?5 w/v) potentiated the muscle contractions and the excitatory post-synaptic potential (EPSP), the optimum concentration being about 10^?5 w/v. 10^?8 w/v Phen. HCl increased miniature EPSP frequency, but this increase became less pronounced as the concentration was raised, and no increase at all was observed at 10^?5 w/v. There was no change in miniature EPSP amplitude at any concentration. Higher concentrations of Phen. HCl (> 2·5 × 10^?6 w/v) depressed the neurally evoked contraction, the EPSP, and the response of the muscle to iontophoretically applied l-glutamate. A gradual increase in muscle input conductance was observed on perfusion with these high concentrations of Phen. HCl. The presence of magnesium in the bathing fluid (15 m-moles/l.) reduced the effectiveness of Phen. HCl in potentiating the EPSP and delayed or reduced the increase in input conductance observed on perfusion with high concentrations of Phen. HCl.The results indicate that low concentrations of Phen. HCl act presynaptically, possibly by depolarizing the excitatory nerve terminals. Higher concentrations may act directly on the post-synaptic glutamate receptors.     

Detecting substrate engagement: responses of tarsal campaniform sensilla in cockroaches

Sensory signals of contact and engagement with the substrate are important in the control and adaptation of posture and locomotion. We characterized responses of campaniform sensilla, receptors that encode forces as cuticular strains, in the tarsi (feet) of cockroaches using neurophysiological techniques and digital imaging. A campaniform sensillum on the fourth tarsal segment was readily identified by its large action potential in nerve recordings. The receptor discharged to contractions of the retractor unguis muscle, which engages the pretarsus (claws and arolium) with the substrate. We mimicked the effects of muscle contractions by applying displacements to the retractor apodeme (tendon). Sensillum firing did not occur to unopposed movements, but followed engagement of the claws with an object. Vector analysis of forces suggested that resisted muscle contractions produce counterforces that axially compress the tarsal segments. Close joint packing of tarsal segments was clearly observed following claw engagement. Physiological experiments showed that the sensillum responded vigorously to axial forces applied directly to the distal tarsus. Discharges of tarsal campaniform sensilla could effectively signal active substrate engagement when the pretarsal claws and arolium are used to grip the substrate in climbing, traversing irregular terrains or walking on inverted surfaces.     

Chemical sensitivity of the hyperneural nerve-muscle preparation of the American cockroach

The hyperneural muscle of Periplaneta americana responded with sustained contracture to applications of l-glutamic acid at near 10^?4 M. d-glutamic acid was much less active. The responses of a particular preparation to glutamate were usually extremely consistent and highly reproducible; however, some preparations showed no response to l-glutamic acid even at 10^?2 M whereas neurally evoked responses were normal. High magnesium, low calcium perfused onto the preparations blocked neurally evoked contractions. The glutamate response was blocked reversibly in low calcium solutions. suggesting that the glutamate effect, when present, was presynaptic.Dopamine, acetylcholine, 5-hydroxytryptamine, synephrine, Rogitine^®, strychnine, strychnine, pentobarbital, and picrotoxin, all suspected to varying degrees of some action on insect central or peripheral synaptic transmission, had no effect on the patterns of neurally evoked contracture of the hyperneural muscle. A new transducer is described for use with low force insect muscle contractions.     

Experimental studies upon a bundle of tonic fibres in the locust extensor tibialis muscle

The bundle of tonic fibres situated at the proximal end of the locust metathoracic extensor tibialis muscle is innervated by the dorsal unpaired median neurone (DUMETi) as well as by the slow excitatory (SETi)) and common inhibitor (CI) neurones. It is not innervated by the fast excitatory neurone (FETi).These fibres contract spontaneously and rhythmically. The myogenic rhythm can be modified by neural stimulation.Spontaneous slow depolarizing potentials resembling the pacemaker potentials of insect cardiac muscle were demonstrated in these fibres.The actions of glutamate on the tonic muscle fibres are not compatible with its being a specific excitatory transmitter. Glutamate can stimulate weak contractions of the muscle, but this action is inhibited when chloride ions are removed from the saline.10^?6 M Octapamine hyperpolarizes the tonic fibre membrane. Octopamine, GABA and glutamate all inhibit the myogenic contractions and reduce the force of the neurally evoked contractions.The tonic muscle is very responsive to proctolin. At 5 × 10^?11 M proctolin enhances the force and increases the frequency of myogenic contractions. At 10^?9 M it depolarizes the muscle membrane potential, and at that and higher concentrations it causes the muscle to contract. At 2 × 10^?7 M proctolin induces contractures which resemble those evoked by sustained high-frequency neural stimulation. Iontophoretic experiments show that proctolin receptors occur at localized sites on the tonic fibre membrane.     

Sequential developmental programmes for retractor muscles of a caenogastropod: reappraisal of evolutionary homologues

Evolutionary changes in the development of shell-attached retractor muscles in gastropods are of fundamental importance to theories about the early evolution and subsequent diversification of this molluscan class. Development of the shell-attached retractor muscle (columellar muscle) in a caenogastropod has been studied at the ultrastructural level to test the hypothesis of homology with the post-torsional left retractor muscle (larval velar retractor) in vetigastropod larvae. The vetigastropod muscle has been implicated in the generation of ontogenetic torsion, a morphogenetic twist between body regions that is important to theories about early gastropod evolution. Two shell-attached retractor muscles develop sequentially in the caenogastropod, Polinices lewisii, which is a pattern that has been also identified in previous ultrastructural studies on a vetigastropod and several nudibranch gastropods. The pattern may be a basal and conserved characteristic of gastropods. I found that the first-formed retractor in larvae of P. lewisii is comparable to the larval velar retractor that exists at the time of ontogenetic torsion in the vetigastropod, Haliotis kamtschatkana. However, the post-metamorphic columellar muscle of P. lewisii is derived exclusively from part of the second-formed muscle, which is comparable to the second-formed pedal muscle system in the vetigastropod. I conclude that the post-metamorphic columellar muscle of P. lewisii, is not homologous to the larval velar retractor of the vetigastropod, H. kamtschatkana.     

Effects of the venom of Philanthus triangulum F. (Hym. sphecidae) and β- and δ-philanthotoxin on axonal excitability and synaptic transmission in the cockroach CNS

This paper provides answers to the questions which of the toxins present in the venom of the wasp Philanthus triangulum may be responsible for the previously reported blockage of transmission through the sixth abdominal ganglion of the cockroach, and whether this may occur by block of synaptic transmission or by affecting axonal exitability. In current clamp experiments the crude venom induces a slight depolarization of the membrane of the giant axon from the sixth abdominal ganglion of the cockroach and a small and irreversible decrease in the amplitude of the action potential. These marginal effects are not seen with relatively high concentrations of the philanthotoxins β-PTX and δ-PTX. It appears that neither the crude venom nor the toxins significantly affect the excitability of the cockroach giant axon. At a concentration of 20 μg ml^?1 δ-PTX causes a slowly reversible block of synaptic transmission from the cercal nerve XI to a giant interneuron without any change in resting membrane potential, whereas β-PTX is inactive. Iontophoretically evoked acetylcholine potentials of the giant neuron are more sensitive to δ-PTX than excitatory postsynaptic potentials. This suggests that the toxin acts on the postsynaptic membrane.     

Action of different toxins from the scorpion Androctonus australis on a locust nerve-muscle preparation

The neuromuscular effects of four purified toxins and crude venom from the scorpion Androctonus australis were investigated in the extensor tibiae nerve-muscle preparation of the locust Locusta migratoria. Insect and crustacean toxin and the mammal toxins I and II which have previously been shown to act on fly larvae, isopods, and mice all paralyse locust larvae. The paralytic potencies decrease in the following order: insect toxin → mammal toxin I → crustacean toxin → mammal toxin II.The toxins and crude venom cause repetitive activity of the motor axons. This leads to long spontaneous trains of junction potentials in the case of crude venom and insect toxin. The other toxins chiefly cause short bursts of action and junction potentials following single stimuli.The ‘slow’ excitatory motor axon invariably is affected sooner than the inhibitory or the ‘fast’ excitatory one. The minimal doses of toxins required to affect the ‘slow’ motor axon decrease in an order somewhat different from that established for their paralytic potencies: insect toxin → crustacean toxin → mammal toxin I → mammal toxin II.Crude venom depolarises and destabilises the muscle membrane potential at low doses. At high doses it decreases the membrane resistance, whereas insect toxin leads to an increase.Crude venom and insect toxin enhance the frequency of mejps, whereas mammal toxin I leads to the occurrence of ‘giant’ mejps.The pattern of axonal activities indicates that the various peripheral branches of the motor nerve are the primary target of the toxins.The time course of nerve action potentials is affected by mammal toxin I and crustacean toxin which cause anomalous shapes and prolongations not caused by insect toxin.The results with other animals suggest that only the insect toxin is selective in its activity. The way it affects the axon might be quite different from that previously reported for scorpion venoms or toxins.     

“Intracisternal microtubules” in neurons of dog ganglia

Summary The changes which occur in the ultrastructure of the mesothoracic retractor unguis muscle of the cockroach Periplaneta americana as a result of disuse are described. Breakdown of myofibrils, sarcoplasmic reticulum, and mitochondria are all marked, this degeneration only being apparent 9 weeks after the operation.     

Characterization of the neurotoxic constituents of Conus geographus (L) venom

The crude venom of the marine gastropod Conus geographus (L) has been separated into three lethal constituents and their actions at the mammalian neuromuscular junction examined.Chromatography of the venom of Sephadex G-50 gave one toxic fraction, which was resolved by ion exchange chromatography on SP-Sephadex into three toxic components. These components were individually purified by diafiltration and Sephadex G-15 chromatography to give Toxins I,II and III. Toxins I and II in concentrations greater than 5 ug/ml reduced the amplitude of end-plate potentials and miniature end-plate potentials; Toxin I also blocked the depolarization of muscle fibres produced by carbachol; neither toxin affected the generation of action potentials in muscle fibres. Toxin III in concentrations greater than 5 ug/ml rapidly and reversibly blocked the generation of action potentials in muscle fibres; it had no effect on resting membrane potential nor on the amplitude of epps or mepps. It also slowly blocked the compound action potential recorded from isolated sciatic nerves but this was not reversible in the experiments. The rate at which this toxin blocked action potentials was increased by stimulation of the preparation. It is suggested that Toxin III acts by blocking the inward movement of sodium during activity. Toxin III appeared to be a nonadeca or eicosa peptide possibly having a cystine residue in the N-terminal position.     

Segment-specific retention of a larval neuromuscular system and its role in a new, rhythmic, pupal motor pattern in Manduca sexta

At pupation in Manduca sexta, accessory planta retractor muscles and their motoneurons degenerate in segment-specific patterns. Accessory planta retractor muscles in abdominal segments 2 and 3 survive in reduced form through the pupal stage and degenerate after adult emergence. Electromyographic and electrophysiological recordings show that these accessory planta retractor muscles participate in a new, rhythmic `pupal motor pattern' in which all four muscles contract synchronously at ∼4 s intervals for extended bouts. Accessory planta retractor muscle contractions are driven by synaptic activation of accessory planta retractor motoneurons and are often accompanied by rhythmic activity in intersegmental muscles and spiracular closer muscles. The pupal motor pattern is influenced by descending neural input although isolated abdominal ganglia can produce a pupal motor pattern-like rhythm. The robust pupal motor pattern first seen after pupal ecdysis weakens during the second half of pupal life. Anemometric recordings indicate that the intersegmental muscle and spiracular closer muscle component of the pupal motor pattern produces ventilation. Accessory planta retractor muscle contractions lift the flexible abdominal floor, to which the developing wings and legs adhere tightly. We hypothesize that, by a bellows-like action, the accessory planta retractor muscle contractions circulate hemolymph in the appendages. Morphometric analysis shows that dendritic regression is similar in accessory planta retractor motoneurons with different pupal fates, and that accessory planta retractor motoneurons begin to participate in the pupal motor pattern while their dendrites are regressed. Accepted: 29 March 1998     

Neuromuscular modulation in Limulus by both octopamine and proctolin

Both octopamine and proctolin potentiate nerve-evoked skeletal muscle contractions in the horseshoe crab, Limulus. The threshold concentration for octopamine was 10^?9 to 10^?8M, while for proctolin it was 3 × 10^?9M. Norepinephrine and dopamine produced effects similar to octopamine but at higher thresholds; tyramine and serotonin were ineffective. Octopamine caused significant increases in amplitudes of excitatory postsynaptic potentials (epsps) of muscle fibers, but had little effect on muscle fiber input resistance or membrane potential. Also, octopamine did not affect depolarization of muscle fibers and subsequent contraction due to the direct action of exogenously applied glutamate. These results suggest that octopamine potentiates nerve-evoked contractions primarily by facilitating release of neuromuscular transmitter. At concentrations above 10^?7M, however, octopamine sometimes caused muscle spikes in response to motoneuron stimulation, a finding that suggests that octopamine may also have some postsynaptic action. Proctolin potentiated the muscle contractions evoked by glutamate but had little effect on glutamate-evoked muscle fiber depolarization, muscle fiber input resistance, or membrane potential. Thus, proctolin appears to act directly on skeletal muscle to enhance contractility. The proctolin-induced potentiations of contraction were sometimes accompanied by modest increases in epsp amplitude, so that unlike lobster skeletal and Limulus cardiac neuromuscular preparations, proctolin may have a secondary direct synaptic effect. Both octopamine and proctolin have been found in Limulus cardiac ganglion. This potential access to the hemolymph and the relatively low threshold concentrations needed for physiological action suggest that octopamine and proctolin could function as hormonal modulators of neuromuscular function in Limulus.