Show simple item record

dc.contributor.authorRanson, Daniel C
dc.contributor.authorAyoub, Samir S.
dc.contributor.authorCorcoran, Olivia
dc.contributor.authorCasalotti, Stefano O
dc.date.accessioned2022-03-09T12:29:12Z
dc.date.available2022-03-09T12:29:12Z
dc.date.issued2020-02-13
dc.identifier.citationRanson, D.C., Ayoub, S.S., Corcoran, O., Casalotti, S.O. (2020) Pharmacological targeting of the GABAB receptor alters Drosophila's behavioural responses to alcohol. Addiction Biology. 2020;25 https://doi.org/10.1111/adb.12725en
dc.identifier.issn1355-6215en
dc.identifier.pmid30761704 (pubmed)
dc.identifier.doi10.1111/adb.12725en
dc.identifier.urihttp://hdl.handle.net/2436/624640
dc.description© 2020 The Authors. Published by Wiley. This is an open access article available under a Creative Commons licence. The published version can be accessed at the following link on the publisher’s website: https://doi.org/10.1111/adb.12725en
dc.description.abstractWhen exposed to ethanol, Drosophila melanogaster display a variety of addiction-like behaviours similar to those observed in mammals. Sensitivity to ethanol can be quantified by measuring the time at which 50% of the flies are sedated by ethanol exposure (ST50); an increase of ST50 following multiple ethanol exposures is widely interpreted as development of tolerance to ethanol. Sensitivity and tolerance to ethanol were measured after administration of the gamma-aminobutyric acid receptor B (GABAB) agonist (SKF 97541) and antagonist (CGP 54626), when compared with flies treated with ethanol alone. Dose-dependent increases and decreases in sensitivity to ethanol were observed for both the agonist and antagonist respectively. Tolerance was recorded in the presence of GABAB drugs, but the rate of tolerance development was increased by SKF 97451 and unaltered in presence of CGP 54626. This indicates that the GABAB receptor contributes to both the sensitivity to ethanol and mechanisms by which tolerance develops. The data also reinforce the usefulness of Drosophila as a model for identifying the molecular components of addictive behaviours and for testing drugs that could potentially be used for the treatment of alcohol use disorder (AUD).en
dc.description.sponsorshipThis work was carried out at the University of East London with the support of a PhD Studentship awarded to DCR from the Society for the Study of Addiction.en
dc.formatapplication/pdfen
dc.languageeng
dc.language.isoenen
dc.publisherWileyen
dc.relation.urlhttps://onlinelibrary.wiley.com/doi/10.1111/adb.12725en
dc.rightsLicence for published version: Creative Commons Attribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectaddiction behavioursen
dc.subjectalcohol use disorderen
dc.subjectCGP 54626en
dc.subjectGABA(B) receptoren
dc.subjectSKF 97541en
dc.subjectdrosophila melanogasteren
dc.titlePharmacological targeting of the GABAB receptor alters Drosophila's behavioural responses to alcoholen
dc.typeJournal articleen
dc.identifier.eissn1369-1600
dc.identifier.journalAddiction Biologyen
dc.date.updated2022-03-09T07:22:23Z
dc.contributor.institutionMedicines Research Group, University of East London, London, UK.
dc.identifier.articlenumbere12725
pubs.place-of-publicationUnited States
dc.date.accepted2019-01-17
rioxxterms.fundersociety for the study of addictionen
rioxxterms.identifier.project2017 PhD Studentshipen
rioxxterms.versionVoRen
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by/4.0/en
rioxxterms.licenseref.startdate2022-03-09en
dc.source.volume25
dc.source.issue2
dc.description.versionPublished version
refterms.dateFCD2022-03-09T12:29:02Z
refterms.versionFCDVoR
refterms.dateFOA2022-03-09T12:29:13Z


Files in this item

Thumbnail
Name:
Pharmacological targeting of the ...
Size:
924.8Kb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record

Licence for published version: Creative Commons Attribution 4.0 International
Except where otherwise noted, this item's license is described as Licence for published version: Creative Commons Attribution 4.0 International