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Behav Neurosci ; 125(5): 705-13, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21942433

ABSTRACT

Various lines of evidence suggest that disruptions in brain dopamine (DA) transmission produce behavioral impairments that can be overcome by salient response-eliciting environmental stimuli. We examined here whether D1 receptor blockade within striatal or frontal cortical DA target regions would differentially affect head entry responses elicited by an auditory cue compared with those occurring during noncued intertrial intervals. Rats received 2 drug-free 28-trial daily sessions in which an auditory cue was immediately followed by food delivery. On the following day, separate groups of rats received bilateral infusions of D1 antagonist SCH23390 to the dorsomedial striatum (DMS), nucleus accumbens (NAcc) core, or the medial prefrontal cortex (mPFC). SCH23390 infused into the DMS and NAcc core suppressed noncued head entries but had no effect on head entries in response to the auditory cue. SCH23390 infused to the mPFC did not reduce either cued or noncued approach responses. Systemic administration of the drug, in contrast, reduced the frequency of both cued and noncued approaches. The results are consistent with the notion that has emerged from the Parkinson's literature that reduced DA transmission produces behavioral suppression that can be overcome by salient environmental response elicitors, and extends this notion by showing that D1 receptor transmission within the striatum strongly suppresses noncued responses while leaving the identical behavior intact when cued by an environmental stimulus.


Subject(s)
Cues , Dopamine Antagonists/pharmacology , Motor Activity/physiology , Prefrontal Cortex/physiology , Receptors, Dopamine D1/antagonists & inhibitors , Receptors, Dopamine D1/physiology , Animals , Benzazepines/pharmacology , Motor Activity/drug effects , Prefrontal Cortex/drug effects , Rats , Rats, Sprague-Dawley
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