Literature DB >> 3404204

Spatial patterns of olfactory bulb single-unit responses to learned olfactory cues in young rats.

D A Wilson1, M Leon.   

Abstract

1. Neonatal rat pups were classically conditioned to an odor stimulus from postnatal day 1 (PN1) to PN18. Tactile stimulation (stroking) was used as the unconditioned stimulus. On PN19, mitral/tufted cell single-unit responses to the conditioned odor were examined in both conditioned and control pups. Recordings were made from mitral/tufted cells in two regions of the olfactory bulb: 1) an area typically associated with focal [14C]2-deoxyglucose (2-DG) uptake in response to the conditioned odor and 2) an area distant from focal 2-DG uptake to the conditioned odor. Animals were anesthetized with urethane and were naturally respiring during the single-unit recording procedure. 2. Changes in mitral/tufted cell firing rate in response to odors in both bulbar regions and all training groups were classified as either excitatory, suppressive, or no response. This response classification was used to compare response patterns to the conditioned odor between bulbar regions and training groups. 3. Classical conditioning selectively modified the response patterns of mitral/tufted cells to the conditioned odor when those cells were associated with regions of focal 2-DG uptake for that odor. Mitral/tufted cells demonstrated significantly more suppressive and fewer excitatory responses to the conditioned odor than cells in control pups. Response patterns to a novel odor were not similarly modified. 4. Response patterns of mitral/tufted cells distant from the focal region of 2-DG uptake to the conditioned odor were not modified by conditioning compared with control pups. 5. The difference in response pattern between cells in the 2-DG focus and cells distant to the 2-DG focus was apparent within 500 ms of the stimulus onset. Given the respiratory rate of these pups (2 Hz), these data suggest that the modified response pattern occurred on the first inhalation of the learned odor. 6. These data demonstrate that both spatial and temporal patterns of olfactory bulb output neuron activity are used in the coding of olfactory information in the bulb. Furthermore, these spatial/temporal response patterns can be modified by early learning.

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Year:  1988        PMID: 3404204     DOI: 10.1152/jn.1988.59.6.1770

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  38 in total

1.  Olfactory fingerprints for major histocompatibility complex-determined body odors.

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2.  Molecular biology of early olfactory memory.

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3.  Low-dimensional chaos maps learning in a model neuropil (olfactory bulb).

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4.  Informatics approaches to functional MRI odor mapping of the rodent olfactory bulb: OdorMapBuilder and OdorMapDB.

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5.  Neural correlates of olfactory learning: Critical role of centrifugal neuromodulation.

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Review 6.  Plasticity in the olfactory system: lessons for the neurobiology of memory.

Authors:  D A Wilson; A R Best; R M Sullivan
Journal:  Neuroscientist       Date:  2004-12       Impact factor: 7.519

7.  Exposure to a broad range of odorants decreases cell mortality in the olfactory bulb.

Authors:  Cynthia C Woo; Edna E Hingco; Gordon E Taylor; Michael Leon
Journal:  Neuroreport       Date:  2006-05-29       Impact factor: 1.837

8.  Associative Processes in Early Olfactory Preference Acquisition: Neural and Behavioral Consequences.

Authors:  Regina M Sullivan; Donald A Wilson; Michael Leon
Journal:  Psychobiology (Austin, Tex)       Date:  1989

9.  Unique Characteristics of Neonatal Classical Conditioning: The Role of the Amygdala and Locus Coeruleus.

Authors:  Regina M Sullivan
Journal:  Integr Physiol Behav Sci       Date:  2001-10

10.  Ontogeny of the enhanced fetal-ethanol-induced behavioral and neurophysiologic olfactory response to ethanol odor.

Authors:  Amber M Eade; Paul R Sheehe; Steven L Youngentob
Journal:  Alcohol Clin Exp Res       Date:  2009-11-24       Impact factor: 3.455

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