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dc.contributor.authorMillón-Peñuela, Carmelo 
dc.contributor.authorFlores-Burgess, Antonio 
dc.contributor.authorCastilla-Ortega, María Estela 
dc.contributor.authorGago-Calderón, Belén 
dc.contributor.authorSerrano, Antonia
dc.contributor.authorSturla, Antonella
dc.contributor.authorGarcía-Durán, Laura 
dc.contributor.authorNarváez-Bueno, José Ángel 
dc.contributor.authorFuxe, Kjell
dc.contributor.authorSantín-Núñez, Luis Javier 
dc.contributor.authorDíaz-Cabiale, Zaida 
dc.date.accessioned2018-06-28T06:44:52Z
dc.date.available2018-06-28T06:44:52Z
dc.date.created2018
dc.date.issued2018-06-28
dc.identifier.urihttps://hdl.handle.net/10630/16037
dc.description.abstractGalanin (GAL) is involved in drug abuse and addiction including alcohol intake. In this work, we have analysed the role of the N-terminal GAL fragment (1-15) [GAL(1-15)] in voluntary ethanol consumption in rats using the two-bottle choice paradigm as well as compare the effects of GAL(1-15) with GAL. The two-bottle choice test was used to determine the voluntary ethanol consumption of rats (Castilla-Ortega et al., 2016). Three sets of experiments were conducted. In the first set of experiments, a dose-response curve of GAL(1-15) was performed. Groups of rats (n=7-9) received i.c.v. GAL(1-15) 1 nmol, 3 nmol or vehicle 2, 14 and 24 hours before the measures. In the second set of experiments, the effects in two-bottle choice test of GAL 3 nmol, and GAL(1-15) 3 nmol were compared. In the last set of experiments rats received i.c.v. GAL(1-15) 3nmol combined with GALR2 antagonist M871 3 nmol 2 hours before the measures. GAL(1-15) 3nmol significantly decreased the alcohol intake 2 (p<0.05), 14 (p<0.05) and 24 (p<0.05) hours after its administration. Moreover, 2 hours after i.c.v. GAL(1-15) 3nmol a significantly decreased by 90% in preference was observed (p<0.05). This effect was maintained 24hours. GAL(1-15) also significantly reduced the alcohol intake (p<0.05) and preference (p<0.05) compared with GAL. GALR2 antagonist M871 significantly blocked the decreased in the ethanol intake (p<0.05) and preference (p<0.05) induced by GAL(1-15) 2 hours after its administration. These results indicates that GAL(1-15) induces a strong reduction in preference and alcohol consumption in rat, showing a differential role than GAL. These results may give basis for the development of novel therapeutic strategies using GAL(1-15) for treatment of alcohol addiction.en_US
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Tech. This study was supported by Spanish SAF2016-79008-P and PPIT.UMA.B1.2017/17.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPéptidosen_US
dc.subjectAlcoholismoen_US
dc.subject.otherGalaninen_US
dc.subject.otherGalanin (1-15)en_US
dc.subject.otherAlcoholismen_US
dc.subject.otherAddictionen_US
dc.titleGalanin n-terminal fragment (1-15) decreases the voluntary alcohol intake in ratsen_US
dc.typeinfo:eu-repo/semantics/conferenceObjecten_US
dc.centroFacultad de Medicinaen_US
dc.relation.eventtitleCINP 31st World Congressen_US
dc.relation.eventplaceViena, Austriaen_US
dc.relation.eventdate16/06/2018 al 19/06/2018en_US


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