TTX sensitive plateau potentials in the crayfish slowly adapting stretch receptor neuron

Summary Electrophysiological experiments showed that a tetrodotoxin (TTX) sensitive slowly inactivating Na⁺ current contributed to the excitability of the sensory neuron (SN1) that innervates the slow receptor muscle in the abdominal muscle receptor (MR1) of crayfish, Procambarus clarkii. Following either tetraethylammonium (TEA) blockage of the K⁺ delayed rectifier currents or exposure to high temperature, a depolarizing plateau potential was evoked by the slow Na⁺ current. Ca⁺⁺ substitution by other divalent cations had no effect on the plateau potential, demonstrating that Ca⁺⁺ is not involved in plateau potential genesis. Simultaneous intrasomatic and extraaxonic recordings coupled with 4-aminopyridine (4-AP) exposure indicated that the slowly inactivating Na⁺ current is primarily somatic, and does not contribute significantly to spiking.Abbreviations 4-AP 4-aminopyridine - HAP hyperpolarizing after-potential - MR1 slowly adapting muscle receptor organ - SR1 sensory neuron of MR1 - TEA tetraethylammonium - TTX tetrodotoxin     

Comparison of auditory sense organs in parasitoid Tachinidae (Diptera) hosted by Tettigoniidae (Orthoptera) and homologous structures in a non-hearing Phoridae (Diptera)

The dipteran parasitoids Therobia leonidei and Homotrixa alleni (Tachinidae) use acoustic cues to locate their calling tettigoniid (Ensifera, Orthoptera) hosts. The sexually dimorphic tympanal organs of both fly species are located at the prosternum. For comparison a homologous chordotonal organ in the non-hearing fly Phormia regina, Meigen (Phoridae) is also described. The scolopidial sense organs of the ears have approximately 180 sensory cells in Th. leonidei and 250 cells in H. alleni. Interspecific analysis indicates that the cell number and arrangement might be genus specific in Tachinidae. The mononematic scolopidia, each with one sensory cell, are of different sizes and insert at the tympanal membrane. Large scolopidial units (diameter of sensory cells up to 50 μm) extend longitudinally from the centre of the sensory organ towards the ligament, whereas small units (sensory cell diameter up to 10 μm) are arranged sequentially within the sensory organ. This arrangement is discussed to be a possible basis for frequency discrimination. The ultrastructure of the scolopidia is similar in the hearing and non-hearing flies. In both groups, the majority of scolopales has a diameter from 2 to 2.9 μm, although hearing species have additionally wider scolopales. The homologous chordotonal organ of Ph. regina consists of approximately 55 sensory cells of uniform direction. The data are discussed in comparison to the ears of other Diptera.     

The locust abdominal muscle receptor organ: response characteristics and its role in the control of segmental distance

A single mutipolar receptor cell is located at the dorsal edge of the lateral internal dorsal muscle in each abdominal segment of the locust (Locusta migratoria). Muscle and receptor cell form the abdominal muscle receptor organ. The receptor cell monitors length changes in the intersegmental muscle, and as a consequence also detects the length of an abdominal segment (cuticule and intersegmental membrane).The muscle receptor organ responds in a phasictonic fashion. The phasic component encodes the rate of change in the stimulus independent from the prevailing length of the muscle receptor organ. The tonic component monitors the absolute length of the muscle.Stimulation of a single muscle receptor organ leads to reflex effects on the ipsilateral longitudinal muscles in at least three adjacent segments. Muscles that shorten the abdomen are activated while their extending antagonists receive reduced activity.The reflex activation of the muscles is polysynaptic. Monosynaptic connections between the receptor and the motoneurones were not found.We identified an interneurone that receives monosynaptic input from the muscle receptor organs in at least three adjacent segments. The interneurone excites motorneurones to the longitudinal muscles of the next posterior segment.Abbreviations aMROII abdominal muscle receptor interneurone 1 - AS3 third abdominal segment - AS4 fourth abdominal segment - AS5 fifth abdominal segment - AS6 sixth abdominal segment - EPSP excitatory postsynaptic potential - MN median nerve - MR multipolar receptor cell - MRO muscle receptor organ - N1 tergal nerve - N2 sternal nerve     

The mandibular muscle receptor organ of Homarus gammarus (L.) (crustacea,decapoda)

Summary A muscle receptor organ is present in the mandible of macruran decapods. The mandibular muscle receptor organ (Mand. MRO) of Homarus gammarus (L.) consists of a ribbon of muscle innervated at its ventral insertion by 10–20 multiterminal sensory neurones. The sensory cells have a small number of dendritic processes.The receptor muscle exhibits some structural properties of both fast and slow muscle. The mean sarcomere length is similar to that of the slow abdominal MRO but the receptor muscle in cross section has a punctate distribution of myofibril bundles more typical of fast muscle.This work was supported by Science Research Council grants B/SR/1871 and BR/G/585.     

Zwei Muskelrezeptoren an der Mandibel von Leuctra (Insecta,Plecoptera) — Beispiele für nicht-ciliäre Sinnesorgane mit Tubularkörper-ähnlichen Strukturen

Zusammenfassung Beide Muskelrezeptoren an der Mandibel von Leuctra ziehen vom vorderen Tentorium-Arm zur Mandibel-Basis. Der ventrale Rezeptor besteht aus zwei dünnen Muskelfasern (6 bis 7 m Durchmesser) und mindestens 10 multiterminalen Sinneszellen, deren Dendriten sich im Innern der Fasern verzweigen und an den Z-Scheiben enden. Der dorsale Rezeptor besitzt drei ähnlich dünne Muskelfasern, aber nur eine einzelne multiterminale Sinneszelle. Ihre Dendriten enden im Ansatzgebiet des Muskels, zwischen Muskelfasern und Epidermiszellen.Beide Rezeptoren haben im wesentlichen denselben Feinbau wie bei Coleopteren, jedoch treten — besonders beim dorsalen Rezeptor — in den Dendriten-Enden Strukturen auf, die den Tubularkörpern bei Mechanosensillen ähneln.

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Two muscle receptor organs at the mandible of Leuctra (Insecta, Plecoptera) — examples for non-ciliary sense organs with tubular-body-like structures

Summary The muscle receptor organs of the mandible of Leuctra extend between the anterior tentorial arm and the mandible base. The ventral receptor is composed of two thin muscle fibres (6–7 m in diameter) and at least ten multiterminal sensory cells, the dendrites of which branch in the interior of the fibres and end near the z-bands. The dorsal receptor organ consists of three muscle fibres of similar diameter and only one multiterminal sensory cell. The dendritic ends lie at the distal end of the muscle, where muscle fibres and epidermal cells make contact.Both receptor organs essentially show the same ultrastructural characteristics as in Coleoptera. However, the dorsal receptor organ in particular possesses organelles in its dendritic ends, which look like the tubular bodies in ciliary mechanoreceptors.

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Mit Unterstützung durch die Deutsche Forschungsgemeinschaft     

Ultrastructure of the cephalic sensory organs of adult Pycnophyes dentatus and of the first juvenile stage of P. kielensis (Kinorhyncha, Homalorhagida)

 The ultrastructure of the paired cephalic sensory organs of adult Pycnophyes dentatus and of the first juvenile stage of P. kielensis (Kinorhyncha, Homalorhagida) was investigated by TEM. In both species, each sensory organ is composed of one receptor cell and one enveloping cell which border a common intercellular lumen. A single receptor cilium extends from the receptor cell into this lumen. The cilium expands behind the basal body and branches into numerous processes. A pair of cephalic sensory organs with these characteristics belongs to the ground pattern of, at least, the Pycnophyidae. The sensory organs of these Kinorhyncha correspond closely with the anterior cephalic organs of the Gastrotricha, but differ from the known cephalic receptors of other Nemathelminthes. Currently, it cannot be evaluated conclusively whether the last common ancestor of the Nemathelminthes possessed cephalic sensory organs and, if it did, what these organs looked like. Accepted: 3 December 1996     

The responses of auditory ventral-cord neurons ofLocusta migratoria to vibration stimuli

Summary Most of the auditory neurons in the ventral nerve cord ofLocusta migratoria carry information not only from the tympanal organs but also from the subgenual organs (vibration sensors). Six of the eight neuron types studied electrophysiologically respond to at least these two modalities. Artificial sounds (white noise and pure tones varying in frequency and intensity) and sinusoidal vibration (200 Hz with an acceleration of 15.8 cm/s₂ or 2000 Hz and 87 cm/s₂) were used as stimuli.Complex excitatory and/or inhibitory interactions of the signals from both tympanal organs form the discharge patterns of auditory ventral-cord neurons in response to stimulation with air-borne sound. Normally the input of the ipsilateral sense organ dominates. The response patterns of these same neurons elicited by vibration stimuli are formed differently, as follows: (1) the sensory inputs of all subgenual organs are integrated in the responses of the ventral-cord neurons; in a single neuron they have either excitatory or inhibitory effects, but not both. (2) The more legs vibrated, the larger is the response. (3) The subgenual organs in the middle legs are most effective, those in the hind legs least so. (4) Ipsilateral vibration has more effect than contralateral.The six auditory neurons react to vibration combined with air-borne sound in different ways. The B neuron is the only one inhibited by vibration stimuli. The G neuron has been studied more intensively; because its anatomical arrangement and the location of the endings of the subgenual receptor fibers are known, it could be inferred from effects of transection of the connectives that interneurons are interposed between receptor cells and the G neuron.Part of the program Sonderforschungsbereich 114 (Bionach) Bochum, under the auspices of the Deutsche Forschungsgemeinschaft, with the support of the Slovenic Research Society (RSS)     

The tympanal hearing organ of the parasitoid fly Ormia ochracea (Diptera, Tachinidae, Ormiini)

Tympanate hearing has evolved in at least 6 different orders of insects, but had not been reported until recently in the Diptera. This study presents a newly discovered tympanal hearing organ, in the parasitoid tachinid fly, Ormia ochracea. The hearing organ is described in terms of external and internal morphology, cellular organization of the sensory organ and preliminary neuroanatomy of the primary auditory afferents. The ear is located on the frontal face of the prothorax, directly behind the head capsule. Conspicuously visible are a pair of thin cuticular membranes specialized for audition, the prosternal tympanal membranes. Directly attached to these membranes, within the enlarged prosternal chamber, are a pair of auditory sensory organs, the bulbae acusticae. These sensory organs are unique among all auditory organs known so far because both are contained within an unpartitioned acoustic chamber. The prosternal chamber is connected to the outside by a pair of tracheae. The cellular anatomy of the fly's scolopophorous organ was investigated by light and electron microscopy. The bulba acustica is a typical chordotonal organ and it contains approximately 70 receptor cells. It is similar to other insect sensory organs associated with tympanal ears. The similarity of the cellular organization and tympanal morphology of the ormiine ear to the ears of other tympanate insects suggests that there are potent constraints in the design features of tympanal hearing organs, which must function to detect high frequency auditory signals over long distances. Each sensory organ is innervated by a branch of the frontal nerve of the fused thoracic ganglia. The primary auditory afferents project to each of the pro-, meso-, and metathoracic neuropils. The fly's hearing organ is sexually dimorphic, whereby the tympanal membranes are larger in females and the spiracles larger in males. The dimorphism presumably reflects differences in the acoustic behavior in the two sexes.     

Thermomechanical properties of the stimulus transducing cuticle in the infrared organ of Merimna atrata (Coleoptera,Buprestidae)

The pyrophilous Australian “fire‐beetle” Merimna atrata strongly depends on the occurrence and localization of forest fires for its reproduction. As a special adaptation to its unusual biology, elaborate infrared (IR) organs have evolved in this species. The IR‐organs consist of a specialized cuticular portion, the absorbing area, innervated by a sensory complex. The sensory complex contains a thermosensitive multipolar neuron with a specialized dendritic region, the terminal dendritic mass, and a mechanosensitive unit represented by a chordotonal organ (CO). Evidence for the IR‐receptive function so far has only been provided for the multipolar neuron. Based on morphological data, it has been hypothesized that the CO could also be involved in IR‐reception by measuring minute thermal deformations of the absorbing area. To test this hypothesis, we investigated structural features like cuticle thickness, reduced Young's modulus and hardness of the absorbing area. The results were used in finite element simulations to analyze the thermomechanical behavior and performance of the IR‐organ. Our findings indicate that considerable thermal deformation of the absorbing area occurs, supporting the hypothesis that the CO could function as photomechanical IR‐receptor. Interestingly, at the innervation site of the CO the lowest relative displacements of the absorbing area were found. This may indicate that the CO as putative photomechanic IR‐receptor has not been adapted according to the requirements of highest sensitivity. Probable benefits of the bimodal innervation by a thermosensory and a mechanosensory unit and their possible interaction for an improved performance of the IR‐organ are discussed. J. Morphol. 275:991–1003, 2014. © 2014 Wiley Periodicals, Inc.     

Fine structure of a sensory organ in the arista of Drosophila melanogaster and some other dipterans

Summary The arista, a characteristic appendage of dipteran antennae, consists of 2 short segments at the base and a long distal shaft. A small sensory ganglion, from which arises the aristal nerve, is located proximally in the shaft. The fine structure of the aristal sensory organ was studied in detail in the fruitfly (Drosophila) and for comparison in the housefly (Musca) and the blowfly (Calliphora). In Drosophila, the aristal sense organ consists of 3 identical sensilla that terminate in the hemolymph space of the aristal shaft, and not in an external cuticular apparatus. Each sensillum comprises 2 bipolar neurons and 2 sheath cells; a third sheath cell envelops the somata of all six neurons of the ganglion. The neurons have long slender dendrites with the usual subdivision into an inner and an outer segment. One of the outer segments is highly lamellated and bears small particles (BOSS-structures) on the outside of its cell membrane; the other outer segment is unbranched and has a small diameter. The fine structure of the first dendrite is strongly reminiscent of thermoreceptors known from the antennae of other insects. These thermoreceptors are often coupled with hygroreceptors; however, we can only speculate whether the second dendrite of the aristal organ also has this function. Our present results argue against mechanoreceptive functions, as formerly postulated. The aristal sense organs in Musca and Calliphora are similar to those in Drosophila, but contain more sensilla (12 in Musca, 18 in Calliphora).     

Development of leg chordotonal sensory organs in normal and heat shocked embryos of the cricket Teleogryllus commodus (Walker)

This paper describes the embryonic development of some parts of the sensory peripheral nervous system in the leg anlagen of the cricket Teleogryllus commodus in normal and heat shocked embryos. The first peripheral neurons appear at the 30% stage of embryogenesis. These tibial pioneer neurons grow on a stereotyped path to the central nervous system and form a nerve which is joined by the growth cones of axons that arise later, including those from the femoral chordotonal organ, subgenual organ and tympanal organ. The development of these organs is described with respect to the increase in number of sensory receptor cells and the shape and position of the organs. At the 100% stage of embryogenesis all three organs have completed their development in terms of the number of sense cells and have achieved an adult shape. To study the function of the tibial pioneer neurons during embryogenesis a heat shock was used to prevent their development. Absence of these neurons has no effect on the development of other neurons and organs proximal to them. However, the development of distal neurons and organs guided by them is impaired. The tibial pioneer neurons grow across the segmental boundary between femur and tibia early in development, and the path they form seems to be essential for establishing the correct connections of the distal sense organs with the central nervous system.     

The activity of abdominal stretch receptors during non-giant swimming in the crayfish<Emphasis Type="Italic"> Cherax destructor</Emphasis> and their role in hydrodynamic efficiency

Recordings were made from the nerve innervating the stretch receptors of the abdominal muscle receptor organs and slow extensor muscles of tethered crayfish, Cherax destructor, during so-called non-giant swimming. The stretch receptors were active during the flexor phase of swimming but the duration and pattern of activity varied from cycle to cycle. Their pattern of firing was modified by the activity of the large accessory neurons which make direct inhibitory synapses upon them. Neither the stretch receptors nor the accessory neurons were active during the extensor phase of the cycle. The timing and extent of tailfan movements during the period of stretch receptor activity were measured from video records before and after the stretch receptor nerves were cut in the second to fifth segments. The promotion of the tailfan during flexion was significantly delayed and the minimum angle to which the uropods were remoted at the end of flexion significantly larger in denervated animals. We propose that afferent information from the stretch receptors coordinates the timing and extent of tailfan movements according to variations in the positioning and movement of the abdominal segments such that the hydrodynamic efficiency of the tailfan is enhanced on a cycle by cycle basis during non-giant swimming.Abbreviations A# abdominal segment number - Acc accessory neuron - LUU large unidentified unit - MRO muscle receptor organ - NGS non-giant swimming - SEMN slow extensor motor neuron - SR stretch receptor neuron     

TEM studies on the lattice organs of cirripede cypris larvae (Crustacea, Thecostraca, Cirripedia)

 Lattice organs consist of five pairs of sensory organs situated on the dorsal carapace in cypris larvae of the Crustacea Cirripedia. The lattice organs in cypris larvae of Trypetesa lampas (Acrothoracica) and Peltogaster paguri (Rhizocephala) represent the two main types found in cirripedes, but only minor differences exist at the TEM level. Each lattice organ is innervated by two bipolar, primary receptor cells. The inner dendritic segment of each receptor cell carries two outer dendritic segments. The outer dendritic segments contain modified cilia with a short ciliary segment (9×2+0 structure). Two sheath cells envelop the dendrite except for the distal ends of the outer dendritic segments. This distal end enters a cavity in the carapace cuticle and reaches a terminal pore situated at the far end of the cavity. The cuticle above the cavity is modified. In both species the epicuticle is partly perforated by numerous small pores and the underlying exocuticle is much thinner and less electron dense than the regular exocuticle. Lattice organs very probably have a chemosensory function and are homologous with the sensory dorsal organ of other crustacean taxa. Accepted: 18 August 1998     

The abdominal muscle receptor organ in Astacus leptodactylus (Crustacea)

The structure of both the slow- and the fast-adapting abdominal muscle receptor organ of Astacus leptodactylus is described with particular reference to differences between the two systems. The receptors are composed of a thin muscle that extends from the front edge of one segment to the front edge of the following and a sensory cell connected with this muscle. In the zone where the sensory cells enter their respective muscle, muscle fibers are reduced (zone of relative muscle exclusion = ZRME) and partly replaced by connective tissue. The occurrence of dendritic processes of both the slow and the fast neurons is confined to this zone. The following differences between the two receptor types are established: (1) The fast receptor muscle reveals a smaller sarcomere length than the slow receptor muscle and a higher myosin/actin filament ratio. (2) Muscle fibers that pass the ZRME are always found at its periphery in the fast system, separated from dendritic processes by layers of connective tissue, while in the slow system muscle fibers frequently are intermingled with the sensory elements. (3) The ZRME of the slow receptor is 20-30% longer than that of the fast receptor. (4) The dendritic varicosities of the slow neuron, on an average, contain many more mitochondria than those of the fast neuron. (5) Dendritic processes (fine twigs as well as varicosities) are juxtaposed to the sarcolemma of the muscle fibers only in the slow system; in the fast system dendrites and muscle are spatially separated by connective tissue. It is assumed that these differences between the two receptor types are at least in part responsible for the different thresholds observed in physiological experiments.     

Organization of the vomeronasal organ in a plethodontid salamander

Salamanders in the family Plethodontidae show a unique behavior (nose-tapping) and have unique structures (nasolabial grooves) that may be used specifically to convey chemicals to the vomeronasal organ. The nasal structure of Plethodon cinereus was studied to determine if there is enhanced development of the vomeronasal organ compared with other salamander families that would correlate with use of these unique features. The vomeronasal organ in salamanders is found in a ventrolateral diverticulum of each main olfactory organ. P. cinereus has a more anteriorly placed vomeronasal organ within the diverticulum, and the posterior limit of each nasolabial groove is adjacent to the anterior limit of the vomeronasal organs. This suggests that the grooves deliver chemicals preferentially to the vomeronasal organs instead of to the main olfactory organs. In addition, the vomeronasal sensory epithelium is thickest anteriorly and is at its thinnest at about the level corresponding to the location of the vomeronasal organ in other salamander families. These adaptations suggest a specific mechanism of odorant delivery to the vomeronasal organ in plethodontid salamanders not found in other salamander families.     

Pharmacological evidence for the involvement of the cAMP cascade in sensory fatigue in Drosophila

Summary We have investigated the effect of systemic treatment with drugs that affect the cAMP cascade on the sensory response and sensory fatigue in an identified mechanosensory neuron of Drosophila. Forskolin, an activator of adenylate cyclase, decreases the sensory response of the neuron. H7, an inhibitor of protein kinase, inhibits sensory fatigue. Octopaminergic ligands facilitate sensory fatigue. These results, together with our previous neurogenetic analysis of sensory fatigue in Drosophila (Corfas and Dudai 1990), corroborate the hypothesis that the cAMP cascade is involved in the generation and modulation of sensory fatigue.Abbreviations ANP antero-notopleural (neuron) - CDMF chlordimeform - ISI interstimulus interval     

Role of proneural genes in the formation of the larval olfactory organ of <Emphasis Type="Italic">Drosophila</Emphasis>

In this paper, we address the role of proneural genes in the formation of the dorsal organ in the Drosophila larva. This organ is an intricate compound comprising the multineuronal dome—the exclusive larval olfactory organ—and a number of mostly gustatory sensilla. We first determine the numbers of neurons and of the different types of accessory cells in the dorsal organ. From these data, we conclude that the dorsal organ derives from 14 sensory organ precursor cells. Seven of them appear to give rise to the dome, which therefore may be composed of seven fused sensilla, whereas the other precursors produce the remaining sensilla of the dorsal organ. By a loss-of-function approach, we then analyze the role of atonal, amos, and the achaete-scute complex (AS-C), which in the adult are the exclusive proneural genes required for chemosensory organ specification. We show that atonal and amos are necessary and sufficient in a complementary way for four and three of the sensory organ precursors of the dome, respectively. AS-C, on the other hand, is implicated in specifying the non-olfactory sensilla, partially in cooperation with atonal and/or amos. Similar links for these proneural genes with olfactory and gustatory function have been established in the adult fly. However, such conserved gene function is not trivial, given that adult and larval chemosensory organs are anatomically very different and that the development of adult olfactory sensilla involves cell recruitment, which is unlikely to play a role in dome formation. N. Grillenzoni and V. de Vaux contributed equally to this work.     

Special cutaneous receptor organs of fish. IV. Ampullary organs of the nonelectric catfish, Kryptopterus

Ampullary organs of the transparent catfish, Kryptopterus bicirrhus, are present in large numbers on the head and in a regular pattern of lines on the body and fins. The organs lie in the epidermis, and have a pore that opens to the surface. Flattened cells form a roof and walls. On the floor of the organ there are a “sensory hillock,” composed of spherical receptor cells and columnar supporting cells, and a “secretory hillock” composed of columnar secretory cells. The receptor cells are nonciliated and have only afferent innervation. The organ cavity is filled with jelly. The organs are compared with ampullary organs of the weakly electric fish Eigenmannia, ampullae of Lorenzini of Raja, and small pit organs of Amiurus. Structural characteristics of the ampullary organs of Kryptopterus make them especially suitable for electrophysiological studies.     

Anatomy and ultrastructure of ventral pharyngeal organs and their phylogenetic importance in Polychaeta (Annelida)

Summary Transmission electron microscopic studies were carried out on the ventral pharyngeal organs in Ctenodrilus serratus and Scoloplos armiger. The pharyngeal organs are composed of a muscle bulbus and a tongue-like organ. In both species the muscle bulbus consists of transverse muscle fibres and interstitial cells with voluminous cell bodies and dorsoventral tonofilaments; the investing muscle runs into the tongue-like organ; the nuclei of the investing muscle fibres are located in caudal bulges; salivary glands are not present, but numerous gland cells occur in the bulbus epithelium. The tongue-like organ, however, is formed by lateral folds (C. serratus) or a bridge-like structure (S. armiger). The specific structure of the bulbus muscle is probably a homologous characteristic also occurring in several other polychaete families. The phylogenetic importance of this ventral pharynx is discussed and a hypothesis is suggested to explain the differentiation of certain other ventral pharyngeal organs from this probably primitive type.