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

Psychopharmacology

Volumn 82, Issue 1-2, 1983, Pages 102-106

  Crocker, Ann D ^a   Overstreet, D H ^b  

^a University of Adelaide: North Terrace   (Australia)

^b FLINDERS UNIVERSITY   (Australia)

Author keywords

Catalepsy; Dopamine receptors; Haloperidol; Hyperthyroid; Hypothyroid; Locomotor activity; Propylthiouracil; Thyroxine

Indexed keywords

BUTACLAMOL; DOPAMINE RECEPTOR; HALOPERIDOL; PROPYLTHIOURACIL; SPIPERONE; THYROXINE; THYROXINE I 125;

ANIMAL EXPERIMENT; CATALEPSY; CENTRAL NERVOUS SYSTEM; CORPUS STRIATUM; DRUG BINDING; DRUG EFFICACY; ENDOCRINE SYSTEM; HYPERTHYROIDISM; HYPOTHYROIDISM; LOCOMOTION; MUSCLE; MUSCULOSKELETAL SYSTEM; NONHUMAN; RAT;

ANIMAL; BEHAVIOR, ANIMAL; BODY TEMPERATURE; CATALEPSY; HALOPERIDOL; HUMAN; HYPERTHYROIDISM; HYPOTHYROIDISM; MALE; RATS; RATS, INBRED STRAINS; RECEPTORS, DOPAMINE; SPIPERONE; SUPPORT, NON-U.S. GOV'T; THYROID HORMONES;

EID: 0021369908     PISSN: 00333158     EISSN: 14322072     Source Type: Journal    
DOI: 10.1007/BF00426390     Document Type: Article

References (14)

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11. 2-γ-endorphin
12. Catecholamines: Diminished rate of synthesis in rat brain and hart after thyroxine pretreatment
13. Hyperthyroidism: Specifically increased response to central NA-(a) receptor stimulation and generally increased monoamine turnover in brain