α5GABAA subunit-containing receptors and sweetened alcohol cue-induced reinstatement and active sweetened alcohol self-administration in male rats

Autor:	Toufiqur Rahman, Sherman A. Jones, Guanguan Li, J. Abigail McDonald, Jaren A. Reeves-Darby, James M. Cook, Cassie M. Chandler, Donna M. Platt
Rok vydání:	2019
Předmět:	Male Agonist Sucrose medicine.medical_specialty Alcohol Drinking Drug Inverse Agonism medicine.drug_class Self Administration Alcohol Stimulus (physiology) Article Naltrexone Extinction Psychological Rats Sprague-Dawley 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Internal medicine Animals Medicine Inverse agonist Receptor Pharmacology Ethanol business.industry Imidazoles Receptors GABA-A Rats 030227 psychiatry Endocrinology chemistry Sweetening Agents Conditioning Operant Cues business Self-administration Reinforcement Psychology 030217 neurology & neurosurgery medicine.drug
Zdroj:	Psychopharmacology (Berl)
ISSN:	1432-2072 0033-3158
Popis:	RATIONALE: GABA(A) receptors containing the α5 subunit (i.e., α5GABA(A)) appear to be critically involved in the reinforcing and subjective effects of alcohol. Their role in alcohol relapse remains unknown. OBJECTIVES: Pharmacological approaches were used to probe the role of α5GABA(A) receptors in alcohol seeking induced by re-exposure to an sweetened alcohol-paired cue, as well as in alcohol+sucrose vs. sucrose self-administration. METHODS: For reinstatement studies, rats were trained to self-administer alcohol under a fixed-ratio schedule in which responding was maintained by alcohol+sucrose deliveries and an alcohol-paired stimulus. Sweetened alcohol seeking was extinguished by eliminating solution deliveries and the sweetened alcohol-paired stimulus. During reinstatement tests, animals received pretreatments of an α5GABA(A) inverse agonist (L-655,708) or an agonist (QH-ii-066) prior to sessions in which presentation of the sweetened alcohol-paired stimulus was restored, but no solution was delivered. For self-administration studies, rats were trained to self-administer alcohol+sucrose or sucrose under a fixed-ratio schedule. Once stable, animals received pretreatments of QH-ii-066, L-655,708, the inverse agonist RY-023 or naltrexone. RESULTS: L-655,708 attenuated reinstatement of sweetened alcohol seeking by alcohol+sucrose-paired cues; whereas sweetened alcohol-seeking behavior was augmented by QH-ii-066, albeit at different doses in different rats. Both L-655,708 and RY-023 selectively reduced alcohol+sucrose vs. sucrose self-administration. In contrast, naltrexone reduced both alcohol+sucrose and sucrose self-administration; whereas QH-ii-066 enhanced sucrose self-administration only. CONCLUSIONS: α5GABA(A) receptors play a key role in the modulation of sweetened alcohol cue-induced reinstatement, as well as in alcohol+sucrose but not sucrose self-administration. Inverse agonist activity at α5GABA(A) receptors may offer a novel strategy for both reduction of problematic drinking and the prevention of relapse.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14c6a8e71c7b9626f8f9767503ea87ef https://doi.org/10.1007/s00213-018-5163-6 Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
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