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dc.contributor.author
Miranda Morales, Roberto Sebastián  
dc.contributor.author
Nizhnikov, Michael E.  
dc.contributor.author
Waters, Dustin H.  
dc.contributor.author
Spear, Norman  
dc.date.available
2017-12-27T15:19:22Z  
dc.date.issued
2014-06  
dc.identifier.citation
Miranda Morales, Roberto Sebastián; Nizhnikov, Michael E.; Waters, Dustin H.; Spear, Norman; New evidence of ethanol's anxiolytic properties in the infant rat; Elsevier Science Inc; Alcohol; 48; 4; 6-2014; 367-374  
dc.identifier.issn
0741-8329  
dc.identifier.uri
http://hdl.handle.net/11336/31639  
dc.description.abstract
Ethanol induces appetitive, aversive, and anxiolytic effects that are involved in the development ofethanol use and dependence. Because early ethanol exposure produces later increased responsiveness toethanol, considerable effort has been devoted to analysis of ethanol’s appetitive and aversive propertiesduring early ontogeny. Yet, there is a relative scarcity of research related to the anxiolytic effects ofethanol during early infancy, perhaps explained by a lack of age-appropriate tests. The main aim of thisstudy was to validate a model for the assessment of ethanol’s anxiolytic effects in the infant rat (postnataldays 13e16). The potentially anxiolytic effects of ethanol tested included: i) amelioration of conditionedplace aversion, ii) ethanol intake in the presence of an aversive conditioned stimulus, iii) the inhibitorybehavioral effect in an anxiogenic environment, and iv) innate aversion to a brightly illuminated area in amodified light/dark paradigm. Ethanol doses employed across experiments were 0.0, 0.5, and 2.0 g/kg.Results indicated that a low ethanol dose (0.5 g/kg) was effective in attenuating expression of a condi-tioned aversion. Ethanol intake, however, was unaffected by simultaneous exposure to an aversivestimulus. An anxiogenic environment diminished ethanol-induced locomotor stimulation. Finally, ani-mals given 0.5 g/kg ethanol and evaluated in a light/dark box showed increased time spent in the illu-minated area and increased latency to escape from the brightly lit compartment than rats treated with ahigher dose of ethanol or vehicle. These new results suggest that ethanol doses as low as 0.5 g/kg areeffective in ameliorating an aversive and/or anxiogenic state in preweanling rats. These behavioralpreparations can be used to assess ethanol’s anxiolytic properties during early development.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Science Inc  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Anxiolysis  
dc.subject
Ethanol Motivational Properties  
dc.subject
Conditioned Aversion  
dc.subject
Light/Dark Test  
dc.subject
Infant Rat  
dc.subject.classification
Inmunología  
dc.subject.classification
Medicina Básica  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
New evidence of ethanol's anxiolytic properties in the infant rat  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-12-26T20:37:14Z  
dc.journal.volume
48  
dc.journal.number
4  
dc.journal.pagination
367-374  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
New York  
dc.description.fil
Fil: Miranda Morales, Roberto Sebastián. University Of Binghamton; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Nizhnikov, Michael E.. University Of Binghamton; Estados Unidos  
dc.description.fil
Fil: Waters, Dustin H.. University Of Binghamton; Estados Unidos  
dc.description.fil
Fil: Spear, Norman. University Of Binghamton; Estados Unidos  
dc.journal.title
Alcohol  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.alcohol.2014.01.007  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0741832914000706  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4035812/