Medical Journals

Conditioning Method Determines Patterns of C-fos Expression Following Novel Taste-illness Pairing.

Authors:
  • Wilkins Emily E
  • Bernstein Ilene L

From: University of Washington, Seattle, WA 98195, USA. ewilkins@u.washington.edu

Behavioural brain research

  • Publish Date: Apr 2006
  • ISSN: 0166-4328
  • Volume: 169
  • Issue: 1
  • Pages: 93-7
  • Medium: Print
  • Language: English
  • Citation (JAMA): Wilkins Emily E, Bernstein Ilene L, et al. Conditioning Method Determines Patterns of C-fos Expression Following Novel Taste-illness Pairing.. Behav. Brain Res. Apr 2006;169:93-7

Abstract

Conditioned taste aversions (CTAs) can be established by exposing rats to a novel taste CS through a bottle or through intra-oral (IO) infusion. Lesion studies suggest differences between the two methods in their engagement of brain circuits, as excitotoxic amygdala lesions have no effect on bottle-conditioned CTAs, but eliminate CTAs produced using IO infusion. Fos-like immunoreactivity (FLI) was used to compare patterns of brain activation after pairing CS taste and US drug using bottle and IO methods. Conditioning rats using the bottle method was associated with widespread elevations in FLI throughout the putative CTA circuit (basolateral and central nuclei of amygdala, insular cortex and nucleus of the solitary tract). In contrast, IO conditioning led to activation only in the central nucleus of amygdala. This supports the suggestion of differences in aversion processing as a function of conditioning method and may explain the greater reliance on amygdala of IO-conditioned CTAs due to engagement of a less distributed neural network.

Mesh Headings (Keywords): Administration, Oral, Amygdala, Animals, Association Learning, Avoidance Learning, Behavioral Research, Cerebral Cortex, Conditioning (Psychology), Drinking Behavior, Lithium Chloride, Male, Neural Pathways, Proto-Oncogene Proteins c-fos, Rats, Rats, Long-Evans, Solitary Nucleus, Taste, Tissue Distribution


Check for Full Text / PubMed Unique Identifier (PMID): 16427145


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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