نمایش مختصر رکورد

dc.contributor.authorMohebi, Ehsanen_US
dc.contributor.authorMolavi, Mehdien_US
dc.contributor.authorMohammadzadeh, Mohammaden_US
dc.contributor.authorHosseinzadeh, Hosseinen_US
dc.contributor.authorAmin, Baharehen_US
dc.date.accessioned1399-07-09T08:23:36Zfa_IR
dc.date.accessioned2020-09-30T08:23:36Z
dc.date.available1399-07-09T08:23:36Zfa_IR
dc.date.available2020-09-30T08:23:36Z
dc.date.issued2020-06-01en_US
dc.date.issued1399-03-12fa_IR
dc.date.submitted2019-03-17en_US
dc.date.submitted1397-12-26fa_IR
dc.identifier.citationMohebi, Ehsan, Molavi, Mehdi, Mohammadzadeh, Mohammad, Hosseinzadeh, Hossein, Amin, Bahareh. (2020). Clavulanic acid improves ethanol withdrawal symptoms in rats. Iranian Journal of Basic Medical Sciences, 23(6), 730-736. doi: 10.22038/ijbms.2020.39129.9287en_US
dc.identifier.issn2008-3866
dc.identifier.issn2008-3874
dc.identifier.urihttps://dx.doi.org/10.22038/ijbms.2020.39129.9287
dc.identifier.urihttp://ijbms.mums.ac.ir/article_15478.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/340562
dc.description.abstract<em><strong>Objective(s):</strong></em> Ethanol withdrawal following chronic use, is an important challenge clinically. In this study, the effect of clavulanic acid was evaluated on the symptoms of ethanol withdrawal in rats.<br /> <em><strong>Materials and Methods:</strong></em> Alcohol dependence was induced by the gavage of ethanol (10% v/v, 2 g/kg), twice daily for 10 days. Clavulanic acid (10, 20, 40, and 80 mg/kg) was administered concurrently with ethanol (sub-acute study), or a single dose after ethanol withdrawal (acute study). Six hours after the last dose of ethanol, anxiety was assessed by the elevated plus-maze (EPM). Seizure-like behavior was evaluated by a sub-convulsive dose of pentylenetetrazol (PTZ, 25 mg/kg/IP). Locomotor activity and motor coordination were measured by the open field and rotarod tests, respectively. Lipid peroxidation marker and antioxidant content were assessed through measuring malondialdehyde (MDA) and glutathione (GSH), respectively.<br /><em><strong>Results:</strong></em> The number of entries and time spent on the open arms of EPM decreased during the withdrawal state. Motor coordination and locomotor activity were significantly decreased. In the sub-acute study, clavulanic acid 80 mg/kg increased time spent and the number of entries to the open arms of EPM, in withdrawn animals. Both motor incoordination and locomotor activity reduction were normalized by clavulanic acid (10, 20, 40 and 80 mg/kg). Withdrawal-induced PTZ kindling seizure was also suppressed by all of the doses. MDA increased, while GSH decreased after withdrawal. Clavulanic acid attenuated such changes.<br /><em><strong>Conclusion:</strong></em> Clavulanic acid could prevent the development of alcohol withdrawal-induced anxiety and seizure. Alcohol withdrawal causes oxidative stress which can be prevented by clavulanic acid.en_US
dc.format.extent719
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Basic Medical Sciencesen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ijbms.2020.39129.9287
dc.subjectAlcohol withdrawalen_US
dc.subjectClavulanic aciden_US
dc.subjectElevated plus mazeen_US
dc.subjectOxidative stressen_US
dc.subjectPentylenetetrazolen_US
dc.subjectRaten_US
dc.titleClavulanic acid improves ethanol withdrawal symptoms in ratsen_US
dc.typeTexten_US
dc.typeOriginal Articleen_US
dc.contributor.departmentStudent Research Committee, Sabzevar University of Medical Sciences, Sabzevar, Iranen_US
dc.contributor.departmentDepartment of Internal Medicine, Sabzevar University of Medical Sciences, Mashhad, I.R. Iranen_US
dc.contributor.departmentCellular and Molecular Research Center, Department of Physiology and Pharmacology, Faculty of Medicine, Sabzevar University of Medical Sciences, Sabzevar, Iranen_US
dc.contributor.departmentDepartment of Pharmacodynamics and Toxicology, Pharmaceutical Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, I.R. Iranen_US
dc.contributor.departmentCellular and Molecular Research Center, Department of Physiology and Pharmacology, Faculty of Medicine, Sabzevar University of Medical Sciences, Sabzevar, Iranen_US
dc.citation.volume23
dc.citation.issue6
dc.citation.spage730
dc.citation.epage736
nlai.contributor.orcid0000-0001-6830-6311
nlai.contributor.orcid0000-0002-5250-6092
nlai.contributor.orcid0000-0002-9121-7453


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