ABSTRACT
The organ of mollusc equilibrium - statocyst appears to be the analogue of acoustic-vestibular system in vertebrate animals. In terrestrial pulmonary snail the epithelial lining of statocyst cavity is created by two types of the cells - a small amount of large cells, provided with kinocilia of sensitive cells and considerably a large number of small supporting or inserted cells, covered with the microvilli. By means of transmission and scanning electron microscopy the ultrastructure and intercellular connections of these cells were studied. The sensitive cells have in a certain way structured cytoplasm, which consists of three layers: ectoplasm, granular layer and hyaloplasm. Myelin-like bodies having the granular, vesicular and drop-like formations in the centre appear to be the special structure of the cytoplasm. In the cytoplasm there are areas, saturated with electron dense glycogen granules. On the electronograms sometimes it is observed how the pinocytic vesicles in the supporting cells are created from the diverticulum of plasmatic membrane of sensitive cells. The boundary areas of plasmatic membrane of adjacent cells (sensitive cells with supporting or supporting cells with the support) are also characterized by the presence of specialized contacts, which are analogous to desmosomes in the epithelial tissues, as well as by the existence of cellular desmosomes, interdigitations. Numerous lacunas have been revealed in the intercellular space, which are connected by the thin tubules and ducts resulting in the formation of a complicated configuration of extensive system of communicating with each other lacunae, which have the exit in statocyst cavity.
Subject(s)
Helix, Snails/cytology , Animals , Epithelial Cells/ultrastructure , Gravity Sensing , Helix, Snails/ultrastructureABSTRACT
Statocysts H. Lucorum appear to be the paired formations having a spherical form and locating on dorsolateral surface of pedal ganglia of subesophageal ganglionic complex. Using the method of reconstruction, as well as the method of scanning electron microscopy on paraffin and semithin slices it has been revealed that the epithelial lining of H. Lucorum appears to be a spatially ordered complex, consisting of 13 cell assemblies. in each of them one sensory cell is surrounded by the satellite cells. The sensory cell has a star shape on the front pole of statocyst because of many protoplasmic processes branching off from its body. The other 12 cells have polygonal shape and form three belts around the inside perimeter of statocyst: interior, middle or equatorial and posterior. There are 4 cells in each belt. The sensory cells forming anterior and posterior belts turned out to be displaced in relation to the cells of equatorial belt and for this reason the whole cell structure resembles a brickwork. The distribution of sensory cells on the inner surfce of statocyst creates the structural polarization of this formtion. First of all, this is evidenced by the presence of the sensory cell on the anterior pole of statocyst and by the absence of those on opposite, posterior pole. The topography of each sensory cell on the inner surface of statocyst, the sizes and shapes of the nuclei, the quantity of nucleoli, the peculiarities of cytoplasm vacuolation and interrelation of sensory and supporting cells have been established.
Subject(s)
Helix, Snails/ultrastructure , Imaging, Three-Dimensional/methods , Sensory Receptor Cells/ultrastructure , Animals , Gravity Sensing/physiology , Helix, Snails/physiology , Image Processing, Computer-Assisted/statistics & numerical data , Microscopy, Electron, Scanning , Sensory Receptor Cells/physiologyABSTRACT
Bending, twitching and quivering are different types of tentacle movements observed during olfactory orientation of the snail. Three recently discovered special muscles, spanning along the length of superior tentacles from the tip to the base, seem to be responsible for the execution of these movements. In this study we have investigated the ultrastructure, contractile properties and protein composition of these muscles. Our ultrastructural studies show that smooth muscle fibers are loosely embedded in a collagen matrix and they are coupled with long sarcolemma protrusions. The muscle fibers apparently lack organized SR and transverse tubular system. Instead subsarcolemmal vesicles and mitochondria have been shown to be possible Ca2+ pools for contraction. It was shown that external Ca2+ is required for contraction elicited by high (40 mM) K+ or 10-4 M ACh. Caffeine (5 mM) induced contraction in Ca2+-free solution suggesting the presence of a substantial intracellular Ca2+ pool. High-resolution electrophoretic analysis of columellar and tentacular muscles did not reveal differences in major contractile proteins, such as actin, myosin and paramyosin. Differences were observed however in several bands representing presumably regulatory enzymes. It is concluded that, the ultrastructural, biochemical and contractile properties of the string muscles support their special physiological function.
Subject(s)
Contractile Proteins/metabolism , Helix, Snails/ultrastructure , Muscle Contraction , Muscles/ultrastructure , Animals , Helix, Snails/physiology , Muscles/metabolismABSTRACT
In the procerebrum of terrestrial snails, 5-HT is a key modulatory substance of the generation of synchronous oscillatory activity and odor learning capability. In this study, we have analyzed the characteristics of the 5-HT-immunoreactive (5-HT-IR) innervation of the distinct anatomical regions of the procerebrum of Helix pomatia, applying correlative light- and electron microscopic immunocytochemistry. A dense network of 5-HT-IR innervation was demonstrated in the cell body layer, meanwhile a varicose fiber system of different density occurred in the different neuropil regions. At the ultrastructural level, labeled varicosities were found to contact both procerebral cell bodies, and different unlabeled axon profiles in the neuropils. The labeled structures established mostly close non-specialized membrane contacts with the postsynaptic profiles. The overall dense distribution of 5-HT-IR innervation supports a general modulatory role of 5-HT in processing different olfactory events.
Subject(s)
Central Nervous System/ultrastructure , Helix, Snails/ultrastructure , Serotonin/metabolism , Animals , Central Nervous System/metabolism , Helix, Snails/metabolism , Immunohistochemistry , SmellABSTRACT
In terrestrial pulmonate snails, cadmium (Cd) uptake leads to the induction of a Cd-specific metallothionein isoform (Cd-MT) that protects against adverse interactions of this toxic metal ion. Increasing concentrations of Cd cause increased individual mortality possibly linked to pathological alterations in the snail midgut gland. Histological, immuno-histochemical, and electron-microscopic methods in combination with tissue metal analyses and quantification of MT induction parameters were applied to the midgut gland of Cd-exposed Roman snails (Helix pomatia). Conspicuous concentration-dependent alterations occurred in this organ, including the metal-induced increase of Cd-MT concentration and manifestation of Cd-MT mRNA precipitations in all midgut gland cell types. The most evident alteration was an increase of cellular turnover reflected by enhanced cell proliferation. Intensified vesiculation of endoplasmic reticulum was noted in basophilic cells and an increasing formation of lipofuscin granules in excretory cells. At the highest Cd concentrations, mitochondrial membranes were disrupted in basophilic cells, and lipofuscin granules were released from excretory cells into the midgut gland tubular system. Some of these alterations (e.g., increased cell proliferation rate, vesiculation of endoplasmic reticulum) detected at low Cd concentrations were interpreted as adaptive response processes enhancing the tolerance of exposed individuals to metal stress. Cellular alterations at higher Cd concentrations (e.g., mitochondrial structural damage) clearly represented ongoing irreversible cellular disruption. Combined evaluation of cellular biomarkers and MT saturation levels indicated that the transition from stress resistance to depletion of resistance capacity occurred above a threshold of 0.8 micromol Cd/g dry weight in the midgut gland of H. pomatia. At these Cd concentrations, Cd-MT was saturated with Cd(2+) ions, whereas at the cellular level, structural alterations turned into pathological deterioration.
Subject(s)
Adaptation, Physiological/drug effects , Animal Structures/cytology , Cadmium/toxicity , Digestive System/cytology , Helix, Snails/cytology , Helix, Snails/drug effects , Stress, Physiological/drug effects , Animal Structures/drug effects , Animal Structures/metabolism , Animal Structures/ultrastructure , Animals , Cadmium/metabolism , Cell Proliferation/drug effects , Digestive System/drug effects , Digestive System/metabolism , Digestive System/ultrastructure , Helix, Snails/ultrastructure , Intracellular Space/drug effects , Intracellular Space/metabolismABSTRACT
The use of manufactured nanoparticles (NPs) is spreading rapidly across technology and medicine fields, posing concerns about their consequence on ecosystems and human health. The present study aims to assess the biological responses triggered by iron oxide NPs (IONPs) and iron oxide NPs incorporated into zeolite (IONPZ) in relation to oxidative stress on the land snail Helix aspersa in order to investigate its use as a biomarker for terrestrial environments. Morphology and structure of both NPs were characterized. Snail food was supplemented with a range of concentrations of IONPs and IONPZ and values of the hemocyte lysosomal membranes' destabilization by 50% were estimated by the neutral red retention (NRRT50) assay. Subsequently, snails were fed with NPs concentrations equal to half of the NRRT50 values, 0.05â¯mgâ¯L-1 for IONPs and 1â¯mgâ¯L-1 for IONPZ, for 1, 5, 10 and 20â¯days. Both effectors induced oxidative stress in snails' hemocytes compared to untreated animals. The latter was detected by NRRT changes, reactive oxygen species (ROS) production, lipid peroxidation estimation, DNA integrity loss, measurement of protein carbonyl content by an enzyme-linked immunoabsorbent assay (ELISA), determination of ubiquitin conjugates and cleaved caspases conjugates levels. The results showed that the simultaneous use of the parameters tested could constitute possible reliable biomarkers for the evaluation of NPs toxicity. However, more research is required in order to enlighten the disposal and toxic impact of iron oxide NPs on the environment to ensure their safe use in the future.
Subject(s)
Environmental Pollutants/toxicity , Ferric Compounds/toxicity , Helix, Snails/drug effects , Hemocytes/drug effects , Lysosomes/drug effects , Metal Nanoparticles/toxicity , Zeolites/toxicity , Administration, Oral , Animals , Comet Assay , DNA Damage , Dose-Response Relationship, Drug , Environmental Monitoring , Environmental Pollutants/administration & dosage , Environmental Pollutants/chemistry , Ferric Compounds/administration & dosage , Ferric Compounds/chemistry , Helix, Snails/metabolism , Helix, Snails/ultrastructure , Hemocytes/metabolism , Hemocytes/ultrastructure , Intracellular Membranes/drug effects , Intracellular Membranes/metabolism , Lipid Peroxidation/drug effects , Lysosomes/metabolism , Lysosomes/ultrastructure , Metal Nanoparticles/chemistry , Metal Nanoparticles/ultrastructure , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Oxidative Stress/drug effects , Particle Size , Protein Carbonylation/drug effects , Surface Properties , Time Factors , Zeolites/administration & dosage , Zeolites/chemistryABSTRACT
A bursa tract diverticulum is widespread in the female part of the hermaphroditic reproductive system of stylommatophoran pulmonates. However, the ultrastructure of the diverticulum is unknown and there is only anecdotal evidence for a spermatophore-dissolving function for this organ. In the present study, we examined the ultrastructure of the diverticulum and investigated histological, histochemical, and morphometric changes at different time intervals after mating in the simultaneously hermaphroditic land snail Arianta arbustorum. The diverticulum in this species of snail is a prominent organ, consisting of a luminal columnar epithelium surrounded by a thick layer of connective tissue. During mating, the diverticulum functions as the site of spermatophore uptake. Within the lumen of the diverticulum the spermatophore wall is dissolved or at least partly broken down. The digested material is taken up by epithelial cells and accumulated in molluscan-specific cells of the connective tissue, the so-called rhogocytes. Subsequent to copulation, the total diameter of the diverticulum increases markedly, reaching a maximum size 12 h after mating, while at the same time the thicknesses of the diverticulum wall and diverticulum epithelium decrease. The length of the diverticulum shows a positive allometry and a high phenotypic variation compared to snail size, which suggests that the diverticulum is under directional sexual selection. We propose that the diverticulum in A. arbustorum has evolved in response to selection pressures imposed by divergent evolutionary interests between male and female function.
Subject(s)
Biological Evolution , Genitalia, Female/physiology , Genitalia, Female/ultrastructure , Helix, Snails/physiology , Helix, Snails/ultrastructure , Animals , Female , Male , Reproduction/physiologyABSTRACT
Distinguishing features of biological constructions are high stability and adaptation to their environment. Beside biocompatibility, nontoxicity and degradability these characteristics are demanded for new biomaterials in the field of tissue engineering. This study investigated the chemical composition, the organization and the in vitro osteoconductive potential of the terrestrial gastropod shell (Helix pomatia) on CAL72 and human osteoblast-like cells. Chemical composition of the biomaterial was examined by X-ray diffraction (XRD) and scanning electron microscopy (SEM) was performed to analyze the architecture of the snail shell and the morphology of the seeded cells. A double staining procedure (FDA/PI) and a proliferation test (EZ4U) assessed the viability of the cells. Microscopical images showed the multilayered architecture of the aragonite shell with hexagonal crystals on the inner side. The cells spread well on the biomaterial and the highest proliferation rate could be measured with CAL72 cells on the inner shell surface. The osteoconductive effects of this natural biomaterial could encourage further experiments in the field of tissue engineering.
Subject(s)
Biocompatible Materials/chemistry , Bone Substitutes/chemistry , Helix, Snails/chemistry , Helix, Snails/ultrastructure , Tissue Engineering/methods , Animals , Bone Matrix/physiology , Bone Matrix/ultrastructure , Calcium Carbonate/chemistry , Calcium Carbonate/therapeutic use , Calcium Phosphates/chemistry , Calcium Phosphates/therapeutic use , Cell Line, Tumor , Cell Proliferation , Cell Survival/physiology , Humans , Microscopy, Electron, Scanning , Osteoblasts/physiology , Osteoblasts/ultrastructure , Osteogenesis/physiology , Tissue Engineering/trends , Tooth/chemistry , Tooth/ultrastructure , Tooth, Artificial/trends , X-Ray DiffractionABSTRACT
The three-dimensional (3D) reconstructions of the di-decameric forms of alpha D and beta C-hemocyanins of the Roman snail Helix pomatia and of the decameric half molecules of alpha D-hemocyanin were carried out on frozen-hydrated specimens observed in the electron microscope by using the random conical tilt series method. The three 3D volumes were examined by computing solid-body surface representations and slices through the volume and by eroding the structure progressively through raising of the threshold. The di-decameric molecule of alpha D and beta C-hemocyanins, reconstructed from side views, are very similar and are composed of a cylindrical wall, comprising ten oblique wall units, and of two collar complexes located at both ends of the cylinder, comprising each five arches and an annular collar made up of five collar units. Erosion of the structure reveals that the wall looks like a segment of a five-stranded right-handed helix and that each oblique wall unit resembles a figure 8 inclined to the right. The decameric half molecule of alpha D-hemocyanin, reconstructed from end-on views, resembles the whole molecule, except that the collar is thinner and appears composed of five independent collar complex units. It is suggested that the difference in structural appearance of the collar complex between the whole and the half alpha D-hemocyanin may be due to the missing cone artifact, induced by the angular limitations imposed by the goniometer of the electron microscope. The comparison between the alpha D-hemocyanin and the beta C-di-decameric hemocyanin at high thresholds suggests that in the beta C-hemocyanin the oblique wall units of each half molecule may be linked by two connections, whereas in alpha D-hemocyanin there may be only one. This difference in the number of connections may be responsible for the lower stability of the alpha D molecule at high salt concentration.
Subject(s)
Helix, Snails/ultrastructure , Hemocyanins/ultrastructure , Animals , Image Processing, Computer-Assisted , Microscopy, Electron , Models, Molecular , Protein Conformation , Species SpecificityABSTRACT
Comparative studies on the nervous system revealed that nitric oxide (NO) retains its function through the evolution. In vertebrates NO can act in different ways: it is released solely or as a co-transmitter, released from presynaptic or postsynaptic site, spreads as a volumetric signal or targets synaptic proteins. In invertebrates, however, the possible sites of NO release have not yet been identified. Therefore, in the present study, the subcellular distribution of the NO synthase (NOS) was examined in the central nervous system (CNS) of two gastropod species, the terrestrial snail, Helix pomatia and the pond snail, Lymnaea stagnalis, which are model species in comparative neurobiology. For the visualization of NOS NADPH-diaphorase histochemistry and an immunohistochemical procedure using a universal anti-NOS antibody were applied. At light microscopic level both techniques labeled identical structures in sensory tracts ramifying in the neuropils of central ganglia and cell bodies of the Lymnaea and Helix CNS. At ultrastructural level NADPH-d reactive/NOS-immunoreactive materials were localized on the nuclear envelope and membrane segments of the rough and smooth endoplasmic reticulum, as well as the cell membrane and axolemma of positive perikarya. NADPH-d reactive and NOS-immunoreactive varicosities connected to neighboring neurons with both unspecialized and specialized synaptic contacts. In the varicosities, the majority of the NADPH-d reactive/NOS-immunoreactive membrane segments were detected in round and pleomorph agranular vesicles of small size (50-200 nm). However, only a small portion (16%) of the vesicles displayed the NADPH-d reactivity/NOS-immunoreactivity. No evidence for the postsynaptic location of NOS was found. Our results suggest that the localization of NADPH-diaphorase and NOS is identical in the snail nervous system. In contrast to vertebrates, however, NO seems to act exclusively in an anterograde way possibly released from membrane segments of the presynaptic transmitter vesicle surface. Based on the subcellular distribution of NOS, NO could be both a volume and a synaptic mediator, in addition NO may function as a co-transmitter.
Subject(s)
Helix, Snails/enzymology , Lymnaea/enzymology , NADPH Dehydrogenase/analysis , Neuropil/enzymology , Nitric Oxide Synthase/analysis , Snails/enzymology , Animals , Central Nervous System/enzymology , Helix, Snails/ultrastructure , Histocytochemistry , Immunohistochemistry , Lymnaea/ultrastructure , Neurons/enzymology , Neurons/ultrastructure , Neuropil/ultrastructure , Snails/ultrastructureABSTRACT
The procerebrum is believed to be important for processing olfactory information and storing olfactory memories in terrestrial pulmonate molluscs. Previous results have demonstrated that the procerebral cell population is morphologically heterogeneous. In the present study, serial sections and electron microscopy were used to investigate differences in synapse distributions. The results demonstrate that procerebral neurons with different sites of arborization have distinct patterns of synapse distribution that probably reflect different functional contributions to the olfactory pathway. Cells that have all their arborizations in the procerebrum, but none in the internal mass, have multiple large varicosities that are specialized for output. On the other hand, cells that arborize in the internal mass or outside the procerebrum have mostly input synapses proximal to the soma and mostly output synapses in the terminal region of the neurites. These cells appear to transmit information from the procerebral cell body mass to other central nervous system regions, e.g., the internal mass and the mesocerebrum. The implications of these data are twofold. Firstly, the procerebrum directly participates in distributing processed olfactory information to more central regions of the nervous system. Secondly, the procerebral neuronal population may be divisible into two subgroups: 1) intrinsically arborizing interneurons; and 2) projection neurons. This is significant because the neural organization of the procerebrum may now be compared with that of olfactory systems in other organisms.
Subject(s)
Helix, Snails/cytology , Animals , Ganglia, Invertebrate/cytology , Ganglia, Invertebrate/ultrastructure , Helix, Snails/ultrastructure , Interneurons/cytology , Interneurons/ultrastructure , Olfactory Pathways/cytology , Olfactory Pathways/ultrastructure , Synapses/ultrastructureABSTRACT
The ultrastructural characteristics of peptidergic peripheral contacts in the snail, Helix pomatia, were investigated, with special attention to the innervation of the heart, buccal mass, and salivary gland by Mytilus inhibitory peptide-immunoreactive neurons. Following the application of correlative light- and electron-microscopic pre-embedding immunocytochemistry, the peripheral tissues reveal a rich innervation by Mytilus inhibitory peptide-immunoreactive elements. These neurons establish three types of neuromuscular contacts in the heart and buccal mass: (1) close (16-20 nm) unspecialized membrane contacts; (2) contacts with a relative wide (40-100 nm) intersynaptic cleft; and (3) labeled varicosties located freely in the extracellular space, far (0. 5-several microm) from the muscle cells. In the salivary gland, the immunoractive profiles contact both the muscular and glandular elements with close (type 1) and wider (type 2) membrane attachments. The great majority of Mytilus inhibitory peptide-immunoreactive profiles contain an ultrastructurally uniform population of large (120-150 nm) electron dense granules. The ultrastructural features of the innervation by Mytilus inhibitory peptide-immunoreactive elements are compared with those established by immunogold labelled FMRFamide-containing profiles in the heart and salivary gland. These latter display similarities in forming the different kinds of intercellular contacts, and differences in the morphological variability of the content of granules in the immunolabeled profiles. The results suggest diverse, non-synaptic modulatory roles of neuropeptides in the peripheral nervous system of Helix pomatia, including localized membrane effects and neurohormonal-like remote global controls, that may also be of significance in orchestrating the effects of neuropeptides released at the same time on different targets.
Subject(s)
Helix, Snails/metabolism , Nervous System/metabolism , Animals , FMRFamide/analysis , Heart/innervation , Helix, Snails/ultrastructure , Immunohistochemistry , Microscopy, Electron , Mouth Mucosa/innervation , Nervous System/ultrastructure , Oligopeptides/analysis , Salivary Glands/innervationABSTRACT
The ultrastructure of the muscle-shell attachment was investigated in the land pulmonate snails Helix aspersa, Anguispira alternata, in the freshwater pulmonate Laevipex sp., and in the freshwater prosobranch Pomacea paludosa. In all cases, a collagenous intercellular matrix and a specialized epithelium (tendon cells) intervene between the columellar muscle and the shell. These tendon cells are characterized by hemidesmosomes at both apical and basal ends, connected by thick bundles of microfilaments. The tendon cells do not insert into the shell directly by microvilli, as formerly thought, but by an extensive network of extracellular organic fibers.
Subject(s)
Helix, Snails/ultrastructure , Muscles/ultrastructure , Snails/ultrastructure , Animals , Microscopy, Electron , Species Specificity , Tendons/ultrastructureABSTRACT
The fine structural and cytochemical characteristics of sensory nerve cells have been studied in the lip of Helix pomatia. A ruthenium red positive cuticular layer was found on the surface of the sensory epithelium. Among the undifferentiated epithelial cells two types of sensory dendrites were observed, namely ciliated and non-ciliated ones. A large amount of smooth surfaced endoplasmic reticulum, microtubes and ribosomes were present in the neuroplasm of the sensory dendrites. However, rough surfaced endoplasmic reticulum, mitochondria, and electrodense bundles of long filaments were characteristic in the simple epithelial cells. The cell bodies of the sensory dendrites lie subepithelially among the muscle cells and they generally contain empty or dense core vesicles.
Subject(s)
Helix, Snails/ultrastructure , Nerve Endings/ultrastructure , Animals , Cilia/ultrastructure , Dendrites/ultrastructure , Endoplasmic Reticulum/ultrastructure , Epithelium/innervation , Epithelium/ultrastructure , Microvilli/ultrastructure , Mouth/innervation , Neurons/ultrastructure , Ruthenium RedABSTRACT
Recording of the integrative electrical activity of the retina of the snail and electron microscopic study of its eye have shown the following. The electrical activity of the photoreceptors is a source of the retinogram (ERG) of the snail. ERG reaction form is characterized by two phases of a response: the initial spike and the following slow fading. For each given value of the photometric brightness of a light signal there exists a low limit of its length, beginning from which the ERG reaction of the snail assumes the form described. The value of the ERG response is a logarithmic function of brightness of the light stimulus.
Subject(s)
Helix, Snails/physiology , Retina/physiology , Vision, Ocular/physiology , Animals , Dark Adaptation/physiology , Electroretinography , Helix, Snails/ultrastructure , In Vitro Techniques , Membrane Potentials/physiology , Microscopy, Electron , Photic Stimulation/methods , Photoreceptor Cells/physiology , Photoreceptor Cells/ultrastructure , Retina/ultrastructureABSTRACT
By electrophysiological and microanatomical methods of analysis of snail CNS small neurones it was shown that a number of neurones form a monosynaptic connection (MSC) with the gigantic polyfunctional neurone LPa3. By using cobalt and nickel staining, the structure of MSC cells LPa7--LPa3 was studied. Six identified synapses in two LPa3 processes zones were found. Physiological analysis showed that the revealed MSC was plastic. The described MSC with identified synapses is convenient for studying synaptic transmission mechanisms.
Subject(s)
Central Nervous System/physiology , Helix, Snails/physiology , Synapses/physiology , Animals , Central Nervous System/ultrastructure , Helix, Snails/ultrastructure , In Vitro Techniques , Membrane Potentials/physiology , Microelectrodes , Neuronal Plasticity/physiology , Receptors, Neurotransmitter/physiology , Receptors, Neurotransmitter/ultrastructure , Staining and Labeling/methods , Synapses/ultrastructureABSTRACT
Recently, three novel flexor muscles (M1, M2 and M3) in the posterior tentacles of the snail have been described, which are responsible for the patterned movements of the tentacles of the snail, Helix pomatia. In this study, we have demonstrated that the muscles received a complex innervation pattern via the peritentacular and olfactory nerves originating from different clusters of motoneurons of the cerebral ganglia. The innervating axons displayed a number of varicosities and established neuromuscular contacts of different ultrastructural forms. Contractions evoked by nerve stimulation could be mimicked by external acetylcholine (ACh) and glutamate (Glu), suggesting that ACh and Glu are excitatory transmitters at the neuromuscular contacts. Choline acetyltransferase and vesicular glutamate transporter immunolabeled axons innervating flexor muscles were demonstrated by immunohistochemistry and in Western blot experiments. Nerve- and transmitter-evoked contractions were similarly attenuated by cholinergic and glutamatergic antagonists supporting the dual excitatory innervation. Dopamine (DA, 10â»5 M) oppositely modulated thin (M1/M2) and thick (M3) muscle responses evoked by stimulation of the olfactory nerve, decreasing the contractions of the M1/M2 and increasing those of M3. In both cases, the modulation site was presynaptic. Serotonin (5-HT) at high concentration (10â»5 M) increased the amplitude of both the nerve- and the ACh-evoked contractions in all muscles. The relaxation rate was facilitated suggesting pre- and postsynaptic site of action. Our data provided evidence for a DAergic and 5-HTergic modulation of cholinergic nerves innervating flexor muscles of the tentacles as well as the muscles itself. These effects of DA and 5-HT may contribute to the regulation of sophisticated movements of tentacle muscles lacking inhibitory innervation.
Subject(s)
Helix, Snails/physiology , Neurotransmitter Agents/metabolism , Smell/physiology , Space Perception/physiology , Animals , Blotting, Western , Helix, Snails/ultrastructure , Immunohistochemistry , Microscopy, Electron, Transmission , Motor Neurons/ultrastructure , Movement , Muscles/innervation , Muscles/metabolism , Muscles/ultrastructureABSTRACT
The synaptology of the cell body layer of the olfactory center, procerebrum, was investigated in two prominent terrestrial pulmonate gastropod species, Helix pomatia and Limax valentianus. In addition, the analysis of the 5-HT-immunoreactive innervation, including ultrastructural level, was performed at high resolution in H. pomatia. A highly complex system of synaptic and non-synaptic connections was found in the procerebrum of both species connected to local neuropil areas of different size. The procerebral (globuli) cell perikarya were richly innervated by varicosities meanwhile the axon profiles also established contacts with each other. Synaptic configurations including convergence, divergence and presynaptic modulation were also revealed. The frequent occurrence of unspecialized but close axo-somatic and axo-axonic membrane contacts referring to the modulatory forms of transmitter release were also accompanied by membrane configurations indicative of active exocytosis. In H. pomatia, the cell mass layer was shown to receive a rich 5-HT-immunoreactive innervation, forming a dense network around the cell bodies. At ultrastructural level, 5-HT-immunoreactive varicosities contacted both cell bodies and different unlabeled axon profiles. Our results suggest that the local neuropil regions in the cell body layer are site of local circuits, which may play a decisive role in olfactory integrative processes bound to the procerebrum. The pattern and form of the 5-HT-immunoreactive innervation of extrinsic origin suggest an overall modulatory role in the cell body layer. The results may serve a basis for considering the role of local intercellular events, connected to microcircuits, within the procerebrum cell body layer involved in oscillation activities.