Tracing neural pathways in snail olfaction: From the tip of the tentacles to the brain and beyond

The anatomical organization of the olfactory system of terrestrial snails and slugs is described in this paper, primarily on the basis of experiments using the African snail Achatina fulica. Behavioral studies demonstrate the functional competence of olfaction in mediating food finding, conspecific attraction, and homing. The neural substrate for olfaction is characterized by an extraordinarily large number of neurons relative to the rest of the nervous system, and by the fact that many of them are unusually small. There exist multiple serial and parallel pathways connecting the olfactory organ, located at the tip of the tentacle, with integrative centers in the central nervous system. Our methods of studying these pathways have relied on the selective neural labels horseradish peroxidase and hexamminecobaltous chloride. One afferent pathway contains synaptic glomeruli whose ultrastructure is similar to that of the glomeruli seen in the mammalian olfactory bulb and the insect olfactory lobe. All of the olfactory neuropils, but especially the tentacle ganglion, contain large numbers of morphologically symmetrical chemical synapses. The procerebrum is a unique region of the snail brain that possesses further features analogous with olfactory areas in other animal groups. Olfactory axons from the tentacle terminate in the procerebrum, but the intrinsic neurons do not project outside of it. An output pathway from the procerebrum to the pedal ganglion has been identified and found to consist of inter‐ganglionic dendrites. The major challenge for future studies is to elucidate the pattern of connectivity within, rather than between, the various olfactory neuropils. © 1993 Wiley‐Liss, Inc.

[1]  Bertil Hanström ÜBER DIE SOGENANNTEN INTELLIGENZSPHÄREN DES MOLLUSKENGEHIRNS UND DIE INNERVATION DES TENTAKELS VON HELIX , 1925 .

[2]  P. A. Anderson,et al.  Action potential in neurons of motor nerve net of Cyanea (Coelenterata). , 1983, Journal of neurophysiology.

[3]  E R Kandel,et al.  Input organization of two symmetrical giant cells in the snail brain , 1966, The Journal of physiology.

[4]  A. Spurr A low-viscosity epoxy resin embedding medium for electron microscopy. , 1969, Journal of ultrastructure research.

[5]  R. Chase,et al.  Responses to conspecific chemical stimuli in the terrestrial snail Achatina fulica (Pulmonata: Sigmurethra) , 1978 .

[6]  N. Takeda,et al.  A sex pheromone secreting gland in the terrestrial snail, Euhadra peliomphala , 1979 .

[7]  Alan Gelperin,et al.  Olfactory Processing and Associative Memory: Cellular and Modeling Studies , 1989 .

[8]  N. T. Davis Improved methods for cobalt filling and silver intensification of insect motor neurons. , 1982, Stain technology.

[9]  A. Gelperin Olfactory Basis of Homing Behavior in the Giant Garden Slug, Limax maximus. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[10]  S. Cullheim,et al.  A quantitative light microscopic study of the dendrites of cat spinal γ‐motoneurons after intracellular staining with horseradish peroxidase , 1981, The Journal of comparative neurology.

[11]  R. Vogt,et al.  Expression of pheromone binding proteins during antennal development in the gypsy moth Lymantria dispar , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  R. Croll Modified cobalt staining and silver intensification techniques for use with whole-mount gastropod ganglion preparations. , 1986, Journal of neurobiology.

[13]  R. Chase,et al.  Responses to odors mapped in snail tentacle and brain by [14C]-2- deoxyglucose autoradiography , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  R. Chase,et al.  Autoradiographic evidence for receptor cell renewal in the olfactory epithelium of a snail , 1986, Brain Research.

[15]  B. Jahan-Parwar,et al.  Cobalt mapping of the nervous system: evidence that cobalt can cross a neuronal membrane. , 1980, Journal of neurobiology.

[16]  M. Colonnier,et al.  An electron microscope study of synaptic contacts in the abdominal ganglion of Aplysia californica , 1979, The Journal of comparative neurology.

[17]  M. Burrows,et al.  The morphology of two groups of spiking local interneurons in the metathoracic ganglion of the locust , 1984, The Journal of comparative neurology.

[18]  J. S. Altman,et al.  A silver intensification method for cobalt-filled neurones in wholemount preparations , 1977, Brain Research.

[19]  R. Chase Lessons from snail tentacles , 1986 .

[20]  A. Gelperin,et al.  OLFACTORY INPUTS TO A BURSTING SEROTONERGIC INTERNEURON IN A TERRESTRIAL MOLLUSC , 1981 .

[21]  S. Kataoka Fine structure of the epidermis of the optic tentacle in a slug, Limax flavus L. , 1976, Tissue & cell.

[22]  R. Chase,et al.  Neuronal elements in snail tentacles as revealed by horseradish peroxidase backfilling. , 1983, Journal of neurobiology.

[23]  E. Kandel,et al.  Ultrastructure of the synapses of sensory neurons that mediate the gill-withdrawal reflex inAplysia , 1979, Journal of neurocytology.

[24]  G. Shepherd Synaptic organization of the mammalian olfactory bulb. , 1972, Physiological reviews.

[25]  D. Tank,et al.  Odour-modulated collective network oscillations of olfactory interneurons in a terrestrial mollusc , 1990, Nature.

[26]  R. Chase,et al.  Synaptic innervation of the giant cerebral neuron in sated and hungry snails , 1992, The Journal of comparative neurology.

[27]  D. Emery Fine structure of olfactory epithelia of gastropod molluscs , 1992, Microscopy research and technique.

[28]  R. Chase,et al.  Interganglionic dendrites constitute an output pathway from the procerebrum of the sanil Achatina fulica , 1989, The Journal of comparative neurology.

[29]  S. Snyder,et al.  Odorant-binding protein: localization to nasal glands and secretions. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[30]  J. Hildebrand,et al.  Organization and synaptic ultrastructure of glomeruli in the antennal lobes of the moth Manduca sexta: a study using thin sections and freeze-fracture , 1981, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[31]  R. Chase,et al.  Quantification of ultrastructural symmetry at molluscan chemical synapses. , 1985, Journal of neurobiology.

[32]  Mitchell J. Weiss Neuronal connections and the function of the corpora pedunculata in the brain of the American cockroach, Periplaneta americana (L.) , 1974, Journal of morphology.

[33]  I. Zs.-Nagy,et al.  The fine structure of the procerebrum of pulmonate molluscs, Helix and Limax. , 1970, Tissue & cell.