Effects of naltrexone on alcohol, sucrose, and saccharin binge-like drinking in C57BL/6J mice: a study with a multiple bottle choice procedure
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Altres documents de l'autoria: Morales, Ileana; Rodríguez Borillo, Olga; Font Hurtado, Laura; Pastor Medall, Raúl
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INVESTIGACIONMetadades
Títol
Effects of naltrexone on alcohol, sucrose, and saccharin binge-like drinking in C57BL/6J mice: a study with a multiple bottle choice procedureData de publicació
2020-04Editor
Lippincott, Williams & WilkinsISSN
0955-8810; 1473-5849Cita bibliogràfica
Morales, Ileana; Rodríguez-Borillo, Olga; Font, Laura; Pastor, Raúl. Effects of naltrexone on alcohol, sucrose, and saccharin binge-like drinking in C57BL/6J mice, Behavioural Pharmacology: April 2020 - Volume 31 - Issue 2&3 - p 256-271 doi: 10.1097/FBP.0000000000000553Tipus de document
info:eu-repo/semantics/articleVersió de l'editorial
https://journals.lww.com/behaviouralpharm/Abstract/2020/04000/Effects_of_naltrex ...Versió
info:eu-repo/semantics/submittedVersionParaules clau / Matèries
Resum
Chronic alcohol (ethyl alcohol, EtOH) binging has been associated with long-term neural adaptations that lead to the development of addiction. Many of the neurobiological features of EtOH abuse are shared with other ... [+]
Chronic alcohol (ethyl alcohol, EtOH) binging has been associated with long-term neural adaptations that lead to the development of addiction. Many of the neurobiological features of EtOH abuse are shared with other forms of binging, like pathological feeding. The drinking-in-the-dark (DID) paradigm has been used extensively to study the neurobiology of EtOH binge-like drinking due to its ability to promote high intakes relevant to human behavior. DID can also generate high consumption of other tastants, but this procedure has not been fully adapted to study forms of binging behavior that are not alcohol-driven. In the present study, we used a modified version of DID that uses multiple bottle availability to promote even higher levels of EtOH drinking in male C57BL/6J mice and allows a thorough investigation of tastant preferences. We assessed whether administration of systemic naltrexone could reduce binging on EtOH, sucrose, and saccharin separately as well as in combination. Our multiple bottle DID procedure resulted in heightened levels of consumption compared with previously reported data using this task. We found that administration of the opioid receptor antagonist naltrexone reduced intakes of preferred, highly concentrated EtOH, sucrose, and saccharin. We also report that naltrexone was able to reduce overall intakes when animals were allowed to self-administer EtOH, sucrose, or saccharin in combination. Our modified DID procedure provides a novel approach to study binging behavior that extends beyond EtOH to other tastants (i.e. sucrose and artificial sweeteners), and has implications for the study of the neuropharmacology of binge drinking. [-]
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Behavioural Pharmacology, 2020, vol. 31, no 2/3Proyecto de investigación
Plan de Promoción de la Investigación-UJI: PR00092/B2018-80; Generalitat Valenciana: AICO/2019/202; The Fulbright U.S. Student Program and NIH Training Grant: DC00011Drets d'accés
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