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Modification of the behavioural effects of haloperidol and of dopamine receptor regulation by altered thyroid status.

Abstract
Rats made hypothyroid by the chronic oral administration of 200 mg/kg propylthiouracil were less sensitive to the cataleptic effects of haloperidol (0.1 mg/kg) treatment than were euthyroid rats chronically treated with isotonic saline. However, rats made hyperthyroid by the chronic injection of 200 micrograms/kg thyroxine were not more sensitive to the cataleptic suppressant effects of haloperidol (0.1 mg/kg). Higher doses of haloperidol (1 and 5 mg/kg) produced significantly greater catalepsy in the hyperthyroid rats and significantly reduced catalepsy in the hypothyroid rats. Receptor binding studies carried out on the striata from rats sacrificed 48 h after a 6-day course of chronic haloperidol (0.1 mg/kg once daily) treatment revealed a significant upregulation (increase) of dopamine receptors in the hypothyroid rats only. These findings are consistent with the hypothesis that altered thyroid status can modify the sensitivity of dopamine receptors.
AuthorsA D Crocker, D H Overstreet
JournalPsychopharmacology (Psychopharmacology (Berl)) Vol. 82 Issue 1-2 Pg. 102-6 ( 1984) ISSN: 0033-3158 [Print] Germany
PMID6420818 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Receptors, Dopamine
  • Thyroid Hormones
  • Spiperone
  • Haloperidol
Topics
  • Animals
  • Behavior, Animal (drug effects)
  • Body Temperature
  • Catalepsy (chemically induced)
  • Haloperidol (pharmacology)
  • Humans
  • Hyperthyroidism (psychology)
  • Hypothyroidism (psychology)
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptors, Dopamine (drug effects)
  • Spiperone (metabolism)
  • Thyroid Hormones (physiology)

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