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Conditioned taste aversion and motion sickness in cats and squirrel monkeys
R A Fox1, M Corcoran, K R Brizzee
1Department of Psychology, San Jose State University, CA 95192.
Canadian Journal of Physiology and Pharmacology
|February 1, 1990
Summary
Ablating the area postrema in cats and monkeys prevents conditioned taste aversion induced by drugs but not by motion. This suggests the area postrema is crucial for drug-induced aversion, not motion sickness.
Area of Science:
- Neuroscience
- Behavioral Pharmacology
- Gastroenterology
Background:
- The area postrema is a key chemosensory organ in the brainstem involved in emesis.
- Conditioned taste aversion (CTA) is a learned response to avoid substances that cause illness.
- The role of the area postrema in CTA, particularly for motion sickness, requires further investigation.
Purpose of the Study:
- To investigate the necessity of the area postrema for drug- and motion-induced conditioned taste aversion (CTA).
- To determine if CTA can serve as a valid measure for subemetic motion sickness.
Main Methods:
- Area postrema ablation was performed in cats and squirrel monkeys using thermal cautery.
- Conditioned taste aversion was induced using xylazine (cats) or lithium chloride (monkeys) in both ablated and intact animals.
- Motion-induced CTA was assessed in ablated and intact animals exposed to a vomiting-inducing motion.
Main Results:
- Ablation of the area postrema prevented xylazine- and lithium chloride-induced vomiting and CTA in cats and monkeys.
- Intact animals exhibited vomiting and CTA following drug administration.
- Motion-induced CTA and vomiting were observed in ablated animals, indicating the area postrema is not essential for this form of aversion.
Conclusions:
- The area postrema is critical for drug-induced conditioned taste aversion but not for motion-induced CTA.
- Motion can induce CTA even after area postrema destruction, suggesting alternative neural pathways.
- Caution is advised when interpreting CTA as a measure of nausea, necessitating identification of physiological nausea correlates.

