Baclofen, raclopride, and naltrexone differentially reduce solid fat emulsion intake under limited access conditions

Pharmacology Biochemistry and Behavior

Volumn 89, Issue 4, 2008, Pages 581-590

  Rao, R E ^a   Wojnicki, F H E ^a   Coupland, J ^a   Ghosh, S ^a   Corwin, R L W ^a  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

Author keywords

Binge eating; Binge type behavior; D2 receptors; Dopamine; Fat emulsions; Fat intake; GABAB; Opioid

Indexed keywords

4 AMINOBUTYRIC ACID B RECEPTOR BLOCKING AGENT; BACLOFEN; DOPAMINE 2 RECEPTOR BLOCKING AGENT; LIPID EMULSION; NALTREXONE; OPIATE ANTAGONIST; RACLOPRIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; DOPAMINE RECEPTOR BLOCKING; DRUG EFFECT; DRUG INHIBITION; FAT INTAKE; FEEDING BEHAVIOR; LIPID TRANSPORT; MALE; NONHUMAN; PRIORITY JOURNAL; SPRAGUE DAWLEY RAT;

ANIMALS; BACLOFEN; BULIMIA; DIETARY FATS; DOPAMINE ANTAGONISTS; EATING; EMULSIONS; FEEDING BEHAVIOR; GABA AGONISTS; MALE; NALTREXONE; NARCOTIC ANTAGONISTS; RACLOPRIDE; RATS; RATS, SPRAGUE-DAWLEY;

RATTUS;

EID: 41949102699     PISSN: 00913057     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pbb.2008.02.013     Document Type: Article

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