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Non-topographical contrast enhancement in the olfactory bulb

BACKGROUND: Contrast enhancement within primary stimulus representations is a common feature of sensory systems that regulates the discrimination of similar stimuli. Whereas most sensory stimulus features can be mapped onto one or two dimensions of quality or location (e.g., frequency or retinotopy)...

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Detalles Bibliográficos
Autores principales: Cleland, Thomas A, Sethupathy, Praveen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1368991/
https://www.ncbi.nlm.nih.gov/pubmed/16433921
http://dx.doi.org/10.1186/1471-2202-7-7
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author Cleland, Thomas A
Sethupathy, Praveen
author_facet Cleland, Thomas A
Sethupathy, Praveen
author_sort Cleland, Thomas A
collection PubMed
description BACKGROUND: Contrast enhancement within primary stimulus representations is a common feature of sensory systems that regulates the discrimination of similar stimuli. Whereas most sensory stimulus features can be mapped onto one or two dimensions of quality or location (e.g., frequency or retinotopy), the analogous similarities among odor stimuli are distributed high-dimensionally, necessarily yielding a chemotopically fragmented map upon the surface of the olfactory bulb. While olfactory contrast enhancement has been attributed to decremental lateral inhibitory processes among olfactory bulb projection neurons modeled after those in the retina, the two-dimensional topology of this mechanism is intrinsically incapable of mediating effective contrast enhancement on such fragmented maps. Consequently, current theories are unable to explain the existence of olfactory contrast enhancement. RESULTS: We describe a novel neural circuit mechanism, non-topographical contrast enhancement (NTCE), which enables contrast enhancement among high-dimensional odor representations exhibiting unpredictable patterns of similarity. The NTCE algorithm relies solely on local intraglomerular computations and broad feedback inhibition, and is consistent with known properties of the olfactory bulb input layer. Unlike mechanisms based upon lateral projections, NTCE does not require a built-in foreknowledge of the similarities in molecular receptive ranges expressed by different olfactory bulb glomeruli, and is independent of the physical location of glomeruli within the olfactory bulb. CONCLUSION: Non-topographical contrast enhancement demonstrates how intrinsically high-dimensional sensory data can be represented and processed within a physically two-dimensional neural cortex while retaining the capacity to represent stimulus similarity. In a biophysically constrained computational model of the olfactory bulb, NTCE successfully mediates contrast enhancement among odorant representations in the natural, high-dimensional similarity space defined by the olfactory receptor complement and underlies the concentration-independence of odor quality representations.
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spelling pubmed-13689912006-02-28 Non-topographical contrast enhancement in the olfactory bulb Cleland, Thomas A Sethupathy, Praveen BMC Neurosci Research Article BACKGROUND: Contrast enhancement within primary stimulus representations is a common feature of sensory systems that regulates the discrimination of similar stimuli. Whereas most sensory stimulus features can be mapped onto one or two dimensions of quality or location (e.g., frequency or retinotopy), the analogous similarities among odor stimuli are distributed high-dimensionally, necessarily yielding a chemotopically fragmented map upon the surface of the olfactory bulb. While olfactory contrast enhancement has been attributed to decremental lateral inhibitory processes among olfactory bulb projection neurons modeled after those in the retina, the two-dimensional topology of this mechanism is intrinsically incapable of mediating effective contrast enhancement on such fragmented maps. Consequently, current theories are unable to explain the existence of olfactory contrast enhancement. RESULTS: We describe a novel neural circuit mechanism, non-topographical contrast enhancement (NTCE), which enables contrast enhancement among high-dimensional odor representations exhibiting unpredictable patterns of similarity. The NTCE algorithm relies solely on local intraglomerular computations and broad feedback inhibition, and is consistent with known properties of the olfactory bulb input layer. Unlike mechanisms based upon lateral projections, NTCE does not require a built-in foreknowledge of the similarities in molecular receptive ranges expressed by different olfactory bulb glomeruli, and is independent of the physical location of glomeruli within the olfactory bulb. CONCLUSION: Non-topographical contrast enhancement demonstrates how intrinsically high-dimensional sensory data can be represented and processed within a physically two-dimensional neural cortex while retaining the capacity to represent stimulus similarity. In a biophysically constrained computational model of the olfactory bulb, NTCE successfully mediates contrast enhancement among odorant representations in the natural, high-dimensional similarity space defined by the olfactory receptor complement and underlies the concentration-independence of odor quality representations. BioMed Central 2006-01-24 /pmc/articles/PMC1368991/ /pubmed/16433921 http://dx.doi.org/10.1186/1471-2202-7-7 Text en Copyright © 2006 Cleland and Sethupathy; licensee BioMed Central Ltd.
spellingShingle Research Article
Cleland, Thomas A
Sethupathy, Praveen
Non-topographical contrast enhancement in the olfactory bulb
title Non-topographical contrast enhancement in the olfactory bulb
title_full Non-topographical contrast enhancement in the olfactory bulb
title_fullStr Non-topographical contrast enhancement in the olfactory bulb
title_full_unstemmed Non-topographical contrast enhancement in the olfactory bulb
title_short Non-topographical contrast enhancement in the olfactory bulb
title_sort non-topographical contrast enhancement in the olfactory bulb
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1368991/
https://www.ncbi.nlm.nih.gov/pubmed/16433921
http://dx.doi.org/10.1186/1471-2202-7-7
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