Literature DB >> 6425895

Treatment schedule as a determinant of the development of tolerance to haloperidol.

R J Carey, J DeVeaugh-Geiss.   

Abstract

Three groups of rats received haloperidol 0.5 mg/kg IP twice daily for 20 days, twice daily for 10 days, or every other day for 40 days. The rats in control groups received saline injections according to the same schedules as the experimental groups. During the chronic treatments, spontaneous motor activity was measured as an indicator of behavioral tolerance, and at the completion of treatments, limbic and striatal homovanillic acid (HVA) levels were determined in order to provide a biochemical indication of tolerance. Both of the haloperidol groups on twice-daily injection schedules exhibited a trend towards recovery of spontaneous motor activity during treatment, indicative of behavioral tolerance, as well as reduced HVA levels indicative of near complete biochemical tolerance. The group receiving haloperidol every other day exhibited a trend toward behavioral intolerance to haloperidol, along with elevated HVA levels that indicated a complete absence of tolerance. The suggested importance of treatment schedule rather than cumulative drug dosage in the development of tolerance to haloperidol may have significance to long-term side effects of chronic neuroleptic treatment such as tardive dyskinesia and clinical issues such as drug holidays.

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Year:  1984        PMID: 6425895     DOI: 10.1007/bf00427766

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  17 in total

1.  Tolerance phenomena with neuroleptics catalepsy, apomorphine stereotypies and striatal dopamine metabolism in the rat after single and repeated administration of loxapine and haloperidol.

Authors:  H Asper; M Baggiolini; H R Burki; H Lauener; W Ruch; G Stille
Journal:  Eur J Pharmacol       Date:  1973-06       Impact factor: 4.432

Review 2.  Dopamine and the pathophysiology of dyskinesias induced by antipsychotic drugs.

Authors:  R J Baldessarini; D Tarsy
Journal:  Annu Rev Neurosci       Date:  1980       Impact factor: 12.449

3.  Antischizophrenic drugs: chronic treatment elevates dopamine receptor binding in brain.

Authors:  D R Burt; I Creese; S H Snyder
Journal:  Science       Date:  1977-04-15       Impact factor: 47.728

4.  The effect of drug holidays in an animal model of tardive dyskinesia.

Authors:  J Bannet; R H Belmaker; R P Ebstein
Journal:  Psychopharmacology (Berl)       Date:  1980       Impact factor: 4.530

5.  Influence of drugs on striatal and limbic homovanillic acid concentration in the rat brain.

Authors:  B H Westerink; J Korf
Journal:  Eur J Pharmacol       Date:  1975-08       Impact factor: 4.432

6.  Behavioral supersensitivity to apomorphine and amphetamine after chronic high dose haloperidol treatment.

Authors:  R C Smith; J M Davis
Journal:  Psychopharmacol Commun       Date:  1975

7.  Neuroleptic-induced hypersensitivity of striatal dopamine receptors in the rat as a model of tardive dyskinesias. Effects of clozapine, haloperidol, loxapine and chlorpromazine.

Authors:  A C Sayers; H R Bürki; W Ruch; H Asper
Journal:  Psychopharmacologia       Date:  1975

Review 8.  Tardive dyskinesia: prevalence and risk factors, 1959 to 1979.

Authors:  J M Kane; J M Smith
Journal:  Arch Gen Psychiatry       Date:  1982-04

9.  Tardive dyskinesia: summary of a Task Force Report of the American Psychiatric Association. By the Task Force on Late Neurological Effects of Antipsychotic Drugs.

Authors: 
Journal:  Am J Psychiatry       Date:  1980-10       Impact factor: 18.112

10.  Tolerance of haloperidol catalepsy.

Authors:  C Ezrin-Waters; P Seeman
Journal:  Eur J Pharmacol       Date:  1977-02-07       Impact factor: 4.432

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  8 in total

Review 1.  Antipsychotic dosing: how much but also how often?

Authors:  Gary Remington; Shitij Kapur
Journal:  Schizophr Bull       Date:  2010-07-21       Impact factor: 9.306

2.  Parametric studies of antipsychotic-induced sensitization in the conditioned avoidance response model: roles of number of drug exposure, drug dose, and test-retest interval.

Authors:  Natashia Swalve; Ming Li
Journal:  Behav Pharmacol       Date:  2012-08       Impact factor: 2.293

3.  Intermittent and continuous haloperidol regimens produce different types of oral dyskinesias in rats.

Authors:  R E See; G Ellison
Journal:  Psychopharmacology (Berl)       Date:  1990       Impact factor: 4.530

4.  Persistent vacuous chewing in rats following neuroleptic treatment: relationship to dopaminergic and cholinergic function.

Authors:  B Glenthøj
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

5.  Sensitization to haloperidol-induced suppression of milk intake: effect of interdose interval.

Authors:  D L Wolgin; J Moore
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

6.  Tardive dyskinesia in relation to estimated dopamine D2 receptor occupancy in patients with schizophrenia: analysis of the CATIE data.

Authors:  Kazunari Yoshida; Robert R Bies; Takefumi Suzuki; Gary Remington; Bruce G Pollock; Yuya Mizuno; Masaru Mimura; Hiroyuki Uchida
Journal:  Schizophr Res       Date:  2014-02-01       Impact factor: 4.939

7.  Haloperidol prevents ethanol-stimulated locomotor activity but fails to block sensitization.

Authors:  J Broadbent; N J Grahame; C L Cunningham
Journal:  Psychopharmacology (Berl)       Date:  1995-08       Impact factor: 4.530

Review 8.  Antipsychotic-induced sensitization and tolerance: Behavioral characteristics, developmental impacts, and neurobiological mechanisms.

Authors:  Ming Li
Journal:  J Psychopharmacol       Date:  2016-07-01       Impact factor: 4.153

  8 in total

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