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Functional neuroanatomy of the rhinophore of Aplysia punctata

BACKGROUND: For marine snails, olfaction represents a crucial sensory modality for long-distance reception, as auditory and visual information is limited. The posterior tentacle of Aplysia, the rhinophore, is a chemosensory organ and several behavioural studies showed that the rhinophores can detect...

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Autores principales: Wertz, Adrian, Rössler, Wolfgang, Obermayer, Malu, Bickmeyer, Ulf
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526719/
https://www.ncbi.nlm.nih.gov/pubmed/16597345
http://dx.doi.org/10.1186/1742-9994-3-6
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author Wertz, Adrian
Rössler, Wolfgang
Obermayer, Malu
Bickmeyer, Ulf
author_facet Wertz, Adrian
Rössler, Wolfgang
Obermayer, Malu
Bickmeyer, Ulf
author_sort Wertz, Adrian
collection PubMed
description BACKGROUND: For marine snails, olfaction represents a crucial sensory modality for long-distance reception, as auditory and visual information is limited. The posterior tentacle of Aplysia, the rhinophore, is a chemosensory organ and several behavioural studies showed that the rhinophores can detect pheromones, initiate orientation and locomotion toward food. However the functional neuroanatomy of the rhinophore is not yet clear. Here we apply serotonin-immunohistochemistry and fluorescent markers in combination with confocal microscopy as well as optical recording techniques to elucidate the structure and function of the rhinophore of the sea slug Aplysia punctata. RESULTS: With anatomical techniques an overview of the neuroanatomical organization of the rhinophore is presented. Labelling with propidium iodide revealed one layer of cell nuclei in the sensory epithelium and densely packed cell nuclei beneath the groove of the rhinophore, which extends to about two third of the total length of the rhinophore. Serotonin immunoreactivity was found within the olfactory glomeruli underneath the epithelium as well as in the rhinophore ganglion. Retrograde tracing from the rhinophore ganglion with 4-(4-(dihexadecylamino)styryl)-N-methylpyridinium iodide (DiA) demonstrated the connection of glomeruli with the ganglion. Around 36 glomeruli (mean diameter 49 μm) were counted in a single rhinophore. Fluorimetric measurements of intracellular Ca(2+ )levels using Fura-2 AM loading revealed Ca(2+)-responses within the rhinophore ganglion to stimulation with amino acids. Bath application of different amino acids revealed differential responses at different positions within the rhinophore ganglion. CONCLUSION: Our neuroanatomical study revealed the number and position of glomeruli in the rhinophore and the rhinophore ganglion as processing stage of sensory information. Serotonin-immunoreactive processes were found extensively within the rhinophore, but was not detected within any peripheral cell body. Amino acids were used as olfactory stimuli in optical recordings and induced sensory responses in the rhinophore ganglion. The complexity of changes in intracellular Ca(2+)-levels indicates, that processing of odour information takes place within the rhinophore ganglion. Our neuroanatomical and functional studies of the rhinophore open up a new avenue to analyze the olfactory system in Aplysia.
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spelling pubmed-15267192006-08-04 Functional neuroanatomy of the rhinophore of Aplysia punctata Wertz, Adrian Rössler, Wolfgang Obermayer, Malu Bickmeyer, Ulf Front Zool Research BACKGROUND: For marine snails, olfaction represents a crucial sensory modality for long-distance reception, as auditory and visual information is limited. The posterior tentacle of Aplysia, the rhinophore, is a chemosensory organ and several behavioural studies showed that the rhinophores can detect pheromones, initiate orientation and locomotion toward food. However the functional neuroanatomy of the rhinophore is not yet clear. Here we apply serotonin-immunohistochemistry and fluorescent markers in combination with confocal microscopy as well as optical recording techniques to elucidate the structure and function of the rhinophore of the sea slug Aplysia punctata. RESULTS: With anatomical techniques an overview of the neuroanatomical organization of the rhinophore is presented. Labelling with propidium iodide revealed one layer of cell nuclei in the sensory epithelium and densely packed cell nuclei beneath the groove of the rhinophore, which extends to about two third of the total length of the rhinophore. Serotonin immunoreactivity was found within the olfactory glomeruli underneath the epithelium as well as in the rhinophore ganglion. Retrograde tracing from the rhinophore ganglion with 4-(4-(dihexadecylamino)styryl)-N-methylpyridinium iodide (DiA) demonstrated the connection of glomeruli with the ganglion. Around 36 glomeruli (mean diameter 49 μm) were counted in a single rhinophore. Fluorimetric measurements of intracellular Ca(2+ )levels using Fura-2 AM loading revealed Ca(2+)-responses within the rhinophore ganglion to stimulation with amino acids. Bath application of different amino acids revealed differential responses at different positions within the rhinophore ganglion. CONCLUSION: Our neuroanatomical study revealed the number and position of glomeruli in the rhinophore and the rhinophore ganglion as processing stage of sensory information. Serotonin-immunoreactive processes were found extensively within the rhinophore, but was not detected within any peripheral cell body. Amino acids were used as olfactory stimuli in optical recordings and induced sensory responses in the rhinophore ganglion. The complexity of changes in intracellular Ca(2+)-levels indicates, that processing of odour information takes place within the rhinophore ganglion. Our neuroanatomical and functional studies of the rhinophore open up a new avenue to analyze the olfactory system in Aplysia. BioMed Central 2006-04-06 /pmc/articles/PMC1526719/ /pubmed/16597345 http://dx.doi.org/10.1186/1742-9994-3-6 Text en Copyright © 2006 Wertz et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Wertz, Adrian
Rössler, Wolfgang
Obermayer, Malu
Bickmeyer, Ulf
Functional neuroanatomy of the rhinophore of Aplysia punctata
title Functional neuroanatomy of the rhinophore of Aplysia punctata
title_full Functional neuroanatomy of the rhinophore of Aplysia punctata
title_fullStr Functional neuroanatomy of the rhinophore of Aplysia punctata
title_full_unstemmed Functional neuroanatomy of the rhinophore of Aplysia punctata
title_short Functional neuroanatomy of the rhinophore of Aplysia punctata
title_sort functional neuroanatomy of the rhinophore of aplysia punctata
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526719/
https://www.ncbi.nlm.nih.gov/pubmed/16597345
http://dx.doi.org/10.1186/1742-9994-3-6
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