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Attenuation of cyclophosphamide-induced taste aversions in mice by prochlorperazine, delta 9-tetrahydrocannabinol, nabilone and levonantradol.

Abstract
A series of experiments were performed with adult CD-1 male mice to evaluate the antiemetic effects of several compounds using the conditioned taste aversion procedure. The antiemetics were administered IP immediately prior to a 30-min conditioning trial in which a novel tasting solution (0.3% saccharin) was presented to the subjects. The emetics, apomorphine and the cancer chemotherapeutic drug cyclophosphamide, were given IP immediately after the conditioning trial at doses that induced taste aversions. Three days later the mice received a two bottle preference test (saccharin vs. water) and the percent saccharin consumed of the total fluid intake was calculated. Doses of the phenothiazine antiemetic prochlorperazine (1 and 3 mg/kg) attenuated the aversions produced by 0.3 and 1.0 mg/kg apomorphine. Doses of drugs currently approved or under clinical investigation as antiemetics in conjunction with cancer chemotherapy, i.e., prochlorperazine (1.0 mg/kg), delta 9-tetrahydrocannabinol (0.3 and 1.0 mg/kg) and nabilone (0.01 and 0.03 mg/kg), significantly attenuated the taste aversions induced by cyclophosphamide. Levonantradol at doses of 0.03 and 0.06 mg/kg, however, did not attenuate cyclophosphamide-induced taste aversions. Conditioned taste aversions produced by emetic drugs warrants investigation as a model for evaluating potential antiemetics.
AuthorsM R Landauer, R L Balster, L S Harris
JournalPharmacology, biochemistry, and behavior (Pharmacol Biochem Behav) Vol. 23 Issue 2 Pg. 259-66 (Aug 1985) ISSN: 0091-3057 [Print] United States
PMID2997807 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Phenanthridines
  • nabilone
  • Dronabinol
  • Cyclophosphamide
  • nantradol
  • Apomorphine
  • Prochlorperazine
Topics
  • Animals
  • Apomorphine (pharmacology)
  • Avoidance Learning (drug effects)
  • Cyclophosphamide (antagonists & inhibitors)
  • Dose-Response Relationship, Drug
  • Dronabinol (analogs & derivatives, pharmacology)
  • Male
  • Mice
  • Phenanthridines (pharmacology)
  • Prochlorperazine (pharmacology)
  • Taste (drug effects)

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