Distribution of serotonin-containing neurons in the central nervous system of the snail Helix pomatia

Summary The distribution of serotonin (5HT)-containing neurons in the central nervous system of the snail Helix pomatia has been determined in whole-mount preparations by use of immunocytochemical and in vivo 5,6-dihydroxy-tryptamine labelling. 5HT-immunoreactive neuronal somata occur in all but the buccal and pleural ganglia. Immunoreactive fibres are present throughout the central nervous system. The 5HT-immunoreactive neuronal somata characteristically appear in groups, located mainly in the cerebral, pedal, visceral and right parietal ganglia. The majority of 5HT-immunoreactive neurons is located in the pedal ganglia. Additionally a dense network of 5HT-immunoreactive varicose fibres is found in the neural sheath of the central nervous system including all the nerves and ganglia. The number and distribution of 5HT-immunoreactive neurons correlates with that demonstrated by 5,6-dihydroxytryptamine labelling method.     

Neurons of the central nervous system innervating the lips and oral area of the pond snail

By means of retrograde transport methods, CoCl2 and horseradish peroxidase, localization and morphological peculiarities of the CNS neurons, that innervate lips and oral area, have been studied in the pond snail (Gastropoda). The neurons, sending their processes into the anterior and middle labial nerves, are found nearly in all ganglia of the parapharyngeal nervous ring on the distal and ventral surface. In the cerebral ganglia they situate as several symmetrical groups. Among the neurons revealed, there are cells with rather local distribution of the terminal branches of the processes in the CNS neuropil and neurons with vast branching areas in the neuropil not only of its own ganglion, but also of the neighbouring ones. The problem concerning the zones of possible intersensory interaction in the cerebral ganglia is discussed and presence in them, together with complex reflectory arches, of bisegmental reflectory arches is considered.     

A theory of cerebral learning regulated by the reward system

Hypothetical mechanisms of the neocorticohippocampal system are presented. Neurophysiological and neuroanatomical findings concerning the system are integrated to demonstrate how animals associate sensory stimuli with rewarding actions: (1) cortical plasticity regulated by cholinergic/noradrenergic inputs from the hypothalamic reward system reinforces association connections between the most activated columns in the cortex; (2) the repetitive reinforcement forms association pathways connecting sensory cortical columns activated by the stimuli with motor cortical columns producing the rewarding actions; (3) after the pathways are formed, the cortex is capable of temporarily memorizing the stimuli by producing long-term potentiation through the cortico-hippocampal circuits; and (4) the memory allows the cortex to extend correct association pathways even in an environment where sensory stimuli rapidly change. A mathematical model of parts of the nervous system is presented to quantitatively examine the mechanisms. Membrane characteristics of single neurons are given by the Hodgkin-Huxley electric circuit. According to anatomical data, neural circuits of the neocortico-hippocampal system are composed by connecting populations of the model neurons. Computer simulation using physiological data concerning ion channels demonstrates how the mechanisms work and how to test the hypotheses presented.A preliminary version of this paper was presented at the Fifteenth Annual Meeting of the Japan Neuroscience Society, Tokyo, December 1991     

Dynamics of FMRFamide immunoreactivity in response to physiologically active substances in the central nervous system of the snail, Achatina fulica

1. The changes in FMRFamide (Phe-Met-Arg-Phe-NH2) immunoreactivity in response to incubation in dopamine, serotonin, met-enkephalin, oxytocin, arg-vasopressin and FMRFamide were examined in the central nervous system of the snail, Achatina fulica. 2. When the central nervous system was cultured in medium which contained dopamine and in medium which contained serotonin, the number of immunoreactive neurons increased in the anterior part of the cerebral ganglion and decreased in the sub-esophageal ganglion. 3. When arg-vasopressin was added to the culture medium, the number of immunoreactive neurons increased in the pedal ganglion and decreased in the other sub-esophageal ganglion. 4. By contrast, when the central nervous system was cultured in medium which contained oxytocin, the number of immunoreactive neurons did not increase, but rather decreased, in each ganglion. 5. No changes in immunoreactivity were detected in the central nervous system when it was cultured in medium which contained FMRFamide. 6. It appears, from these results, that the production and release of FMRFamide from different neurons are differentially affected by the physiologically active substances tested.     

Neurofilaments of the neurosecretory cells of a snail

Following brief formaldehyde fixation and detergent extraction numerous neurofilaments (NF) were seen in the nervous system of the gastropod snail Helisoma. NF are present in perikarya, axons and release sites of the neurosecretory (NS) cells. The NS neurons and their axons contain actin and microtubules, stain positively with NBD-phallacidin, and react positively to antibodies against mammalian tubulin, myosin and NF. In the perikarya of colchicine treated cells large masses of NF were seen. Extraction of NF from the nervous system was accomplished by a disassembly and reassembly method.     

Effects of dephosphorylated core of 2',5'-oligoadenylate (2',5'-ApApA) on the electric activity of snail neurons

On nervous ganglion of snail Helix pomatia was shown the effect of dephosphorylated core of 2',5'-oligoadenylate (2',5'-ApApA) on pacemaker electrical activity of RPa2 snail neurons. In experiments, solution of 2',5'-ApApA in concentration 5 x 10(-5) mol/l effected snail nervous ganglion in the course of 2 min then it was washed in the course of 2 hours.     

Distribution and function of an Aplysia cardioexcitatory peptide, NdWFamide, in pulmonate snails

The distribution and function of an Aplysia cardioexcitatory peptide, NdWFamide, were examined in the nervous system of pulmonate snails. We chemically identified the authentic NdWFamide from a land snail (Euhadra congenita) and a freshwater snail (Lymnaea stagnalis). NdWFamide potentiated the heartbeat of those snails. Immunohistochemistry using anti-NdWFamide antibody demonstrated the distribution of NdWFamide-containing neurons and fibers in the central nervous system, as well as peripheral tissues, such as the cardiovascular region and accessory sex organs. These results suggest that NdWFamide is a neuropeptide mediating the neural regulation of the activity of the cardiovascular and reproductive systems of snails.     

FMRFamide immunoreactive neurons in the central nervous system of the snail,Achatin a fulica

• 1.1. FMRFamide immunoreactive neurons were detected in the central nervous system of the snail, Achatina fulica.
• 2.2. FMRFamide immunoreactive neurons were found in all the ganglia comprising the central nervous system. In particular, the immunoreactivity was recognized in both the ordinary and giant neurons of the visceral and right parietal ganglia.
• 3.3. In the cerebral and pleural ganglia, FMRFamide immunoreactive neurons were found only in the ordinary neurons. The immunoreactivity was shown to have a tendency to form a group in the cerebral and pedal ganglia.

     

On the number and spatial distribution of the catecholamine-containing (GA-positive) neurons in some higher and lower turbellarians — a comparison

Original data on the distribution of catecholamines in Provortex karlingi Ax (Rhabdocoela), Microstomum sp. (Macrostomida), and three species of Acoela are presented. Three groups of homologous CA-ergic (catecholaminergic) neurons are discussed: (1) pharyngeal neurons, (2) L-neurons lying postcerebrally in the lateral body regions, and (3) brain neurons. The pharyngeal neurons constitute a synapomorphy of the Rhabditophora. The systematic distribution of the L- and brain neurons, together with the character concerning number of longitudinal nervous trunks, implies that the Catenulida and Rhabditophora are more closely related to each other than to Acoelomorpha. Though these conclusions need confirmation, they show that knowledge of the distribution of neurons containing a given transmitter may be useful for elucidating phylogenetic relationships of lower plathelminths.     

Somatic polyploidy in neurons from gastropod mollusks. I. Morphological characteristics of ganglia and neurons in the CNS of the snail Succinea lauta

A study was made of general anatomy and histological organization of the central nervous system in Succinea lauta, a gastropod pulmonate snail. Neurons grow by means of polyploidy during the postnatal succineid ontogeny. In the adult individuals diameters of perikaria of large neurons increase 2.5 to 5 times, in comparison with young individuals. As a whole, in adult snails sizes of ganglian cells vary from 3 to 380 mkm. Most of giant neurons are in parietal, abdominal and pallial ganglia. The chromatin structure has been described in neurons of young and adult snails. The endomitotic mechanism of polyploidization in the succineid ganglioneurons is proposed.     

Identified neuronal individuals in the buccal ganglia of Helix pomatia.

The buccal ganglia of Helix pomatia are used as model nervous structures in neurophysiological and in epileptological studies. Many basic problems concerning membrane physics, functioning of the single neurons and of neuronal networks can be studied easily using these ganglia. The model character mainly comes from the relative simplicity of this nervous system and that it contains large visually identifiable neurons. As in other invertebrate nervous systems, the large neurons have proved to be individuals showing the same functional and structural properties from one animal to the next.     

The ultrastructure of the central nervous system neurons and synapses in the edible snail under a high concentration of potassium ions]

The morphometric and electron microscopic results on neuronal and synaptic ultrastructure of central nervous system of Helix pomatia snail, incubated in vitro in media with high potassium ion concentration are represented in the present paper. The activation of glial cells is revealed with its close attachment to neurons. The energization of neuronal mitochondria and signs of cytoplasmatic oedema are clearly visible. The penetration of glial endings in the large neuronal branches and the synaptic vesicles confluence in neuronal endings are found.     

Electrical connection between two bursting neurons inHelix pomatia

In some preparations of the CNS ofHelix pomatia, two neurons with bursting activity may be present in the right parietal ganglion, where usually there is only one bursting neuron RPal. If electrical activity of these neurons is recorded simultaneously, fluctuations of membrane potential are almost completely synchronized. Artificial depolarization and hyperpolarization of the membrane of one neuron caused depolarization or hyperpolarization of the other neuron. During long-term recording of the activity of both neurons synchronous modulation of their bursting activity was observed. Modulating factor (a peptide fraction obtained from the water-soluble part of snail brain homogenate) led to potentiation of the bursting activity of both neurons. It is concluded from the results of these experiments that two bursting RPal neurons, connected electrically with one another, may exist in the snail nervous system. In cases when the parameters of pacemaker activity of these two neurons are closely similar, electrical connection guarantees synchronization of their bursting activity and ensures a common frequency of changes in their membrane potential.     

Immunocytochemical identification of serotoninergic neurons in planaria <Emphasis Type="Italic">Girardia tigrina</Emphasis>

Flatworms occupy an important position among simple organisms, which were first in the evolution having bilateral symmetry and centralized nervous system. This paper provides evidence of the presence of a biogenic amine serotonin in free-living flatworms planarians Girardia tigrina (Turbellaria, Platyhelminthes). Using immunohistochemical method, fluorescence and confocal laser scanning microscopy, we have identified serotonin neurons and their fibers using planarian whole-mount preparations and got important information about distribution of serotoninergic components in their body. Information on the number and size of serotonin-immunopositive neurons in the brain ganglion of G. tigrina and on the distribution density of serotoninergic neurons in the central nervous system of worms is presented for the first time. The published data concerning the serotoninergic signalization in flatworms are briefly overviewed.     

The expression pattern of CREB genes in the central nervous system of the pond snail Lymnaea stagnalis

To analyze the expression pattern of genes of cAMP responsive element binding protein (CREB), we performed in situ hybridization for the whole central nervous system (CNS) of the pond snail Lymnaea stagnalis. The CREB1 (activator) and CREB2 (repressor) homologues have already been cloned in L. stagnalis, and they are referred to as LymCREB1 and LymCREB2. Using the frozen sections and the whole mount preparations of the CNS, we mapped the distribution of LymCREB1 and LymCREB2 mRNA containing neurons. The present findings showed that the LymCREB1 mRNA containing neurons are a relatively few, whereas LymCREB2 mRNA is contained ubiquitously in the whole CNS of L. stagnalis.     

Neurogenesis in the procerebrum of the snail Helix aspersa: a quantitative analysis

The procerebrum, a specialized structure for olfaction in terrestrial pulmonate molluscs, contains 20,000 to 50,000 small, uniformly sized neurons that increase in number with age. Here I show the likely source of neurons added to the procerebrum of Helix aspersa and that the rate of neuron addition depends on snail weight. After hatching, during the initial exponential growth phase, H. aspersa adds neurons to the procerebral apex by mitosis and from a cerebral tube. In the logistic growth phase beginning 30-40 days post-hatch, neurons also seem to be added to the procerebrum from the peritentacular and olfactory nerves, causing the rate of neuron addition to approximately double; but as in the earlier exponential growth phase, this rate remains a function of snail weight. This neuron addition throughout the life of the snail can be predicted by snail weight. In the two growth phases, the number of neurons in the procerebrum is given by logarithmic functions of snail weight. The results here for H. aspersa provide the basis for experiments to determine the peripheral origin and destination of neuronal precursors that are added to the procerebrum and to determine how neuron addition affects the function of the procerebrum.     

Morphologic characteristics and responses of the neurons of the right parietal ganglion in Lymnaea stagnalis to stimulation of the sensory structures

Intracellular recordings have been made of the responses of 22 neurons of the central part of the dorsal surface of the right parietal ganglion of the snail Lymnaea stagnalis to adequate stimulation of chemo-, photo- and mechanoreceptor cells of the mantle and head skin including tentacles and lips. It was shown that the main bulk of the neurons investigated has broad receptive fields in the body wall and mantle, being able to respond to all types of the applied stimuli. Alongside, single neurons were revealed which receive single-mode input, either a mechanosensory or chemosensory one. Morphological studies indicate that the neurons are unipolar and have usually one, sometimes several projections. They differ in the pattern of branching as well as in the projections to peripheral nerves. However, almost all of them have vast dendritic regions in the central nervous system including central sensory nucleus of the right parietal ganglion.     

Neuron-specific modulation by serotonin of regenerative outgrowth and intracellular calcium within the CNS of Helisoma trivolvis

We have investigated the cell-specific effect of serotonin (5-HT) on regenerating neurons within the adult central nervous system of the pond snail, Helisoma trivolvis. In culture, 5-HT arrests outgrowth of buccal neurons B19 but not neurons B5 (Haydon, McCobb, and Kater, 1984). After axotomy, neurons within the Helisoma nervous system typically exhibit profuse regenerative outgrowth. This study, on neurons within the CNS, shows that 5-HT selectively inhibits the outgrowth of specific identified neurons, and also causes significant elevations in intracellular calcium concentrations as measured by the calcium indicator dye, Fura-2. The outgrowth of neurons B19 and C1 was selectively inhibited when ganglia were incubated in 5 X 10(-5) M 5-HT. The outgrowth of buccal neurons B5, however, was not affected. Moreover, 5-HT caused significant transient elevations of calcium concentrations in neurons B19 over 30 minutes, but neurons B5 did not show any increases in calcium concentrations with the addition of 5-HT. These results suggest that the effect of 5-HT upon outgrowth of regenerating neurons may be due to an increase in the intracellular calcium concentration.     

Mytilus inhibitory peptides (MIP) in the central and peripheral nervous system of the pulmonate gastropods, Lymnaea stagnalis and Helix pomatia: distribution and physiological actions

The distribution and neuroanatomy of Mytilus inhibitory peptides (MIP)-containing neurons in the central nervous system and their innervation pattern in the peripheral nervous system of the pulmonate snail species, Lymnaea stagnalis and Helix pomatia, have been investigated immunocytochemically, by applying an antibody raised to GSPMFVamide. A significant number of immunoreactive neurons occurs in the central nervous system of both species (Lymnaea: ca 600-700, Helix: ca 400-500), but their distribution is different. In Lymnaea, labeled neurons are found in all central ganglia where a number of large and giant neurons, previously identified physiologically, reveal MIP immunoreactivity. In Helix, most of the immunolabeled neurons are small (12-30 microm) and concentrated in the buccal and cerebral ganglia; the parietal ganglia are free of labeled cells. In both species, the ganglionic neuropils, peripheral nerves, connectives, and commissures are richly supplied with immunolabeled fibers. The MIP-immunoreactive innervation pattern in the heart, intestine, buccal mass and radula, and foot is similar in both species, with labeled axonal bundles and terminal-like arborizations (buccal mass, foot) or a network of varicose fibers (heart, intestine). Intrinsic neurons are not present in these tissues. The application of GSPYFVamide inhibits the spontaneous contractions of the esophageal longitudinal musculature in Helix, indicating the bioactivity of the peptide. An outside-out patch-clamp technique has demonstrated that GSPYFVamide opens the K+ channels in central nerve cells of Helix. Injection of GSPYFVamide into the body cavity inhibits the feeding of starved Helix. A wide modulatory role of MIP at central and peripheral levels is suggested in Lymnaea and Helix, including the participation in intercellular signalling processes and remote neurohormonal-like control effects.