Literature DB >> 26660648

Norepinephrine in prelimbic cortex delays extinction of amphetamine-induced conditioned place preference.

Emanuele Claudio Latagliata1, Pamela Saccoccio2, Chiara Milia2, Stefano Puglisi-Allegra2,3.   

Abstract

RATIONALE: Drug-associated cues exposure to induce extinction is a useful strategy to contrast cue-induced drug seeking. Treatments aimed at reducing motivational properties of cues are considered highly promising since they could decrease their ability to induce drug-conditioned behaviors. Norepinephrine (NE) in the medial prefrontal cortex (mPFC) is critical for attribution of motivational salience to highly salient stimuli, suggesting a major role in prelimbic (PL) mpFC to modulate the motivational properties of drug-related cues, invigorating them, and consequently, delaying extinction.
OBJECTIVES: To investigate if NE in PL fosters the maintenance of drug-seeking behavior, we assessed its role on amphetamine-induced conditioned place preference (CPP). Moreover, to affirm the specificity of NE in PL, we also assessed the role of NE in the infralimbic (IL) mPFC.
METHODS: The effects of selective NE depletion in the PL or in the IL of C57BL/6J mice were assessed on the expression of amphetamine-induced CPP before and after extinction procedure.
RESULTS: NE-depleted mice in PL extinguished preference for Amph-paired chamber long before sham animals. By contrast, IL-depleted animals maintained place preference for more than 4 weeks after the procedure of extinction, having at that moment interrupted the test.
CONCLUSIONS: Inactivation of NE in PL cortex blunts amphetamine-induced CPP, thus fostering extinction and showing to be critical for the maintenance of conditioned Amph-seeking behavior. Opposite effects of NE depletion in IL, seemingly in agreement with literature on extinction, are discussed in terms of balance of activity between PL and IL in extinction.

Entities:  

Keywords:  Amphetamine; Conditioned place preference (CPP); Extinction; Infralimbic cortex; Motivational salience; Norepinephrine; Prelimbic cortex

Mesh:

Substances:

Year:  2015        PMID: 26660648     DOI: 10.1007/s00213-015-4177-6

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


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