Literature DB >> 16470402

Withdrawal from continuous amphetamine administration abolishes latent inhibition but leaves prepulse inhibition intact.

Daria Peleg-Raibstein1, Esther Sydekum, Holger Russig, Joram Feldon.   

Abstract

RATIONALE: Schizophrenia has been associated with dysregulation of dopamine (DA) transmission and impairment in a number of experimental tasks, including sensorimotor gating assessed using prepulse inhibition (PPI) and selective attention assessed using latent inhibition (LI). We have demonstrated in previous studies that after withdrawal from escalating (ESC) dosages of amphetamine (AMPH), animals exhibited disruption of LI but no alteration of PPI. Moreover, these animals always showed behavioural sensitization to an AMPH challenge.
OBJECTIVE: In this study, we were interested in testing whether a different administration schedule would elicit disruption of both LI and PPI.
METHODS: Animals were treated with continuous AMPH release (via osmotic mini-pumps at a dosage of 10 mg kg(-1) day(-1) for 7 days) and tested for their performance in L and PPI during withdrawal in a drug free state. Rats received AMPH treatment during the induction phase in their home cages or in the activity chambers. Following withdrawal, the expression of behavioural sensitization to an AMPH challenge was tested in both cases in the activity chambers.
RESULTS: Animals pretreated with AMPH from both groups did not exhibit behavioural sensitization. Withdrawal from continuous administration induced LI attenuation with no effect on PPI.
CONCLUSIONS: These findings are similar to what was previously found with respect to an ESC AMPH regime. The only difference between the schedules was that the ESC AMPH schedule led to behavioural sensitization whereas the continuous AMPH did not. It is suggested that the expression of sensitization may not be a prerequisite for observed LI disruption.

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Year:  2006        PMID: 16470402     DOI: 10.1007/s00213-005-0286-y

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


  68 in total

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Review 3.  The neurotoxic effects of continuous cocaine and amphetamine in Habenula: implications for the substrates of psychosis.

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4.  Differential performance of acute and chronic schizophrenics in a latent inhibition task.

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Journal:  J Nerv Ment Dis       Date:  1988-10       Impact factor: 2.254

5.  Clozapine and haloperidol reinstate latent inhibition following its disruption during amphetamine withdrawal.

Authors:  Holger Russig; Carol A Murphy; Joram Feldon
Journal:  Neuropsychopharmacology       Date:  2002-06       Impact factor: 7.853

6.  Differential effects of withdrawal from chronic amphetamine or fluoxetine administration on brain stimulation reward in the rat--interactions between the two drugs.

Authors:  D Lin; G F Koob; A Markou
Journal:  Psychopharmacology (Berl)       Date:  1999-08       Impact factor: 4.530

7.  Latent inhibition in drug naive schizophrenics: relationship to duration of illness and dopamine D2 binding using SPET.

Authors:  N S Gray; L S Pilowsky; J A Gray; R W Kerwin
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8.  Further evidence that amphetamines produce long-lasting dopamine neurochemical deficits by destroying dopamine nerve fibers.

Authors:  G A Ricaurte; L S Seiden; C R Schuster
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Review 9.  Effects of typical and atypical antipsychotics on prepulse inhibition in schizophrenia: a critical evaluation of current evidence and directions for future research.

Authors:  Veena Kumari; Tonmoy Sharma
Journal:  Psychopharmacology (Berl)       Date:  2002-06-05       Impact factor: 4.530

10.  The Effects of dizocilpine and phencyclidine on prepulse inhibition of the acoustic startle reflex and on prepulse-elicited reactivity in C57BL6 mice.

Authors:  Benjamin K Yee; D L Tilly Chang; Joram Feldon
Journal:  Neuropsychopharmacology       Date:  2004-10       Impact factor: 7.853

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  1 in total

1.  Baseline prepulse inhibition expression predicts the propensity of developing sensitization to the motor stimulant effects of amphetamine in C57BL/6 mice.

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Journal:  Psychopharmacology (Berl)       Date:  2012-08-17       Impact factor: 4.530

  1 in total

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