5-HT3 receptors are not involved in conditioned taste aversions induced by 5-hydroxytryptamine, ipecacuanha or cisplatin

Eur J Pharmacol. 1998 Jul 10;352(2-3):143-9. doi: 10.1016/s0014-2999(98)00359-8.

Abstract

We have used the rat to examine the involvement of the 5-HT3 receptor in the mechanism(s) of conditioned taste aversion induced by 5-hydroxytryptamine (5-HT) and selected emetic drugs. 5-HT, ipecacuanha and cisplatin all induced conditioned taste aversion at doses known to induce emesis in other species but the responses were resistant to treatment with the 5-HT3 receptor antagonists ondansetron and granisetron. Further, m-chlorophenylbiguanide, a selective and potent 5-HT3 receptor agonist, failed to induce a conditioned taste aversion. The data provide strong evidence that the 5-HT3 receptor is not involved in conditioned taste aversion mechanisms in the rat. Results are discussed in terms of the usefulness of the rat conditioned taste aversion paradigm to anti-emetic research.

MeSH terms

  • Animals
  • Antineoplastic Agents / adverse effects
  • Avoidance Learning / physiology
  • Cisplatin / adverse effects
  • Cisplatin / pharmacology*
  • Conditioning, Classical
  • Drinking Behavior
  • Granisetron / pharmacology
  • Ipecac / pharmacology*
  • Male
  • Ondansetron / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Serotonin / physiology*
  • Receptors, Serotonin, 5-HT3
  • Serotonin / pharmacology*
  • Serotonin Antagonists / pharmacology
  • Taste / physiology*

Substances

  • Antineoplastic Agents
  • Receptors, Serotonin
  • Receptors, Serotonin, 5-HT3
  • Serotonin Antagonists
  • Serotonin
  • Ondansetron
  • Ipecac
  • Cisplatin
  • Granisetron