Vagotomy facilitates extinction of conditioned taste aversions in rats

Results from three experiments indicate that severing the subdiaphragmatic vagus in rats increased the rate of extinction of learned taste aversions. In Experiment 1, although vagotomized rats acquired a saccharin aversion equivalent to that of controls when the illness-inducing agent was the blood-...

Full description

Saved in:
Bibliographic Details
Published inJournal of comparative & physiological psychology Vol. 95; no. 1; p. 114
Main Authors Kiefer, S W, Rusiniak, K W, Garcia, J, Coil, J D
Format Journal Article
LanguageEnglish
Published United States 01.02.1981
Subjects
Online AccessGet more information

Cover

Loading…
More Information
Summary:Results from three experiments indicate that severing the subdiaphragmatic vagus in rats increased the rate of extinction of learned taste aversions. In Experiment 1, although vagotomized rats acquired a saccharin aversion equivalent to that of controls when the illness-inducing agent was the blood-borne toxin apomorphine, vagotomized rats tended to consume more saccharin than controls during repeated extinction tests. In Experiment 2, vagotomy disrupted retention and increased extinction of a preoperatively acquired saccharin aversion. Disruptions were found when the taste aversion was induced by copper sulfate, a local gastric irritant (Experiment 2A), or apomorphine, a systemic toxin (Experiment 2B); in each experiment vagotomized rats consumed more saccharin than controls on the first retention test and extinguished the prior to surgery. Experiment 3 demonstrated that vagotomy did not affect retention or extinction of a shock-induced conditioned emotional response (lick to suppression) to noise. It is concluded that integrity of the vagus is not necessary for acquisition of a learned taste aversion when a blood-borne toxin is used as the ill-inducing agent. However, the vagus apparently mediates an integral portion of the conditioned response following taste-illness acquisition regardless of whether the illness agent is a local gastric irritant or a systemic toxin.
ISSN:0021-9940
DOI:10.1037/h0077751