Literature DB >> 22903071

Drug-drug conditioning between citalopram and haloperidol or olanzapine in a conditioned avoidance response model: implications for polypharmacy in schizophrenia.

Nathan L Sparkman1, Ming Li.   

Abstract

Patients with schizophrenia often have anxiety and depression, and thus are treated with multiple psychotherapeutic medications. This practice of polypharmacy increases the possibility for drug-drug interactions. However, the pharmacological and behavioral mechanisms underlying drug-drug interactions in schizophrenia remain poorly understood. In the present study, we adopted a preclinical approach and examined a less known behavioral mechanism, drug-drug conditioning (DDC) between haloperidol (a typical antipsychotic) or olanzapine (atypical antipsychotic) and citalopram (a selective serotonin reuptake inhibitor). A rat two-way conditioned avoidance response paradigm was used to measure antipsychotic activity and determine how DDC may alter the antipsychotic efficacy in this model. Following acquisition of the avoidance response, rats were then randomly assigned to receive vehicle, citalopram (10.0 mg/kg, intraperitoneally), haloperidol (0.05 mg/kg, subcutaneously), olanzapine (1.0 mg/kg, subcutaneously), combined haloperidol with citalopram, or combined olanzapine with citalopram treatment for seven avoidance test sessions. In comparison with antipsychotic treatment alone, combined treatment with citalopram potentiated the antiavoidance effect of olanzapine or haloperidol (to a lesser extent) during the seven drug-test sessions. In addition, repeated pairing of citalopram with haloperidol or olanzapine caused citalopram to show a newly acquired avoidance-disruptive effect. This effect was context specific because citalopram paired with haloperidol or olanzapine outside the avoidance testing context (i.e. home cages) did not show such an effect. These findings indicate that concurrent antidepressant and antipsychotic treatments may engender a DDC process that follows the general Pavlovian associative conditioning principles. They also indicate that adjunctive citalopram treatment may enhance the antipsychotic efficacy of haloperidol and olanzapine in the treatment of schizophrenia.

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Year:  2012        PMID: 22903071      PMCID: PMC4755296          DOI: 10.1097/FBP.0b013e328358590d

Source DB:  PubMed          Journal:  Behav Pharmacol        ISSN: 0955-8810            Impact factor:   2.293


  48 in total

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4.  Brain region and dose effects of an olanzapine/fluoxetine combination on extracellular monoamine concentrations in the rat.

Authors:  Susanne Koch; Kenneth W Perry; Frank P Bymaster
Journal:  Neuropharmacology       Date:  2004-02       Impact factor: 5.250

5.  Heart rate conditioning with pentobarbital as a conditioned stimulus and amphetamine as an unconditioned stimulus.

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Journal:  Behav Neurosci       Date:  1989-04       Impact factor: 1.912

6.  Biochemical effects and drug levels in rats after long-term treatment with the specific 5-HT-uptake inhibitor, citalopram.

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Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1982-10

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Authors:  P C Waldmeier; A A Delini-Stula
Journal:  Eur J Pharmacol       Date:  1979-05-15       Impact factor: 4.432

9.  Pavlovian conditioning with ethanol and lithium: effects on heart rate and taste aversion in rats.

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Journal:  J Comp Physiol Psychol       Date:  1982-10

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Authors:  H K Taukulis; M T Fillmore; J L Ruggles
Journal:  Pharmacol Biochem Behav       Date:  1992-01       Impact factor: 3.533

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  7 in total

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Journal:  Neuropharmacology       Date:  2013-08-14       Impact factor: 5.250

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5.  Effect of environmental cues on the behavioral efficacy of haloperidol, olanzapine, and clozapine in rats.

Authors:  Tao Sun; Xinfeng Liu; Ming Li
Journal:  Behav Pharmacol       Date:  2014-08       Impact factor: 2.293

6.  Olanzapine sensitization and clozapine tolerance: from adolescence to adulthood in the conditioned avoidance response model.

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Journal:  Neuropsychopharmacology       Date:  2012-11-07       Impact factor: 7.853

Review 7.  Antipsychotic-induced sensitization and tolerance: Behavioral characteristics, developmental impacts, and neurobiological mechanisms.

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  7 in total

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