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Clavulanic acid improves ethanol withdrawal symptoms in rats
OBJECTIVE(S): 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. MATERIALS AND METHODS: Alcohol dependence was induced by the gavage of ethanol (10% v/v, 2 g/kg), tw...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Mashhad University of Medical Sciences
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351446/ https://www.ncbi.nlm.nih.gov/pubmed/32695288 http://dx.doi.org/10.22038/ijbms.2020.39129.9287 |
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author | Mohebbi, Ehsan Molavi, Mehdi Mohammadzadeh, Mohammad Hosseinzadeh, Hossein Amin, Bahareh |
author_facet | Mohebbi, Ehsan Molavi, Mehdi Mohammadzadeh, Mohammad Hosseinzadeh, Hossein Amin, Bahareh |
author_sort | Mohebbi, Ehsan |
collection | PubMed |
description | OBJECTIVE(S): 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. MATERIALS AND METHODS: 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. RESULTS: 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sub-acute study, clavulanic acid 80 mg/kg increased time spent and the number of entries to the open arms of EPM, in withdrawn animals.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. CONCLUSION: 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. |
format | Online Article Text |
id | pubmed-7351446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-73514462020-07-20 Clavulanic acid improves ethanol withdrawal symptoms in rats Mohebbi, Ehsan Molavi, Mehdi Mohammadzadeh, Mohammad Hosseinzadeh, Hossein Amin, Bahareh Iran J Basic Med Sci Research Article OBJECTIVE(S): 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. MATERIALS AND METHODS: 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. RESULTS: 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. CONCLUSION: 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. Mashhad University of Medical Sciences 2020-06 /pmc/articles/PMC7351446/ /pubmed/32695288 http://dx.doi.org/10.22038/ijbms.2020.39129.9287 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Mohebbi, Ehsan Molavi, Mehdi Mohammadzadeh, Mohammad Hosseinzadeh, Hossein Amin, Bahareh Clavulanic acid improves ethanol withdrawal symptoms in rats |
title | Clavulanic acid improves ethanol withdrawal symptoms in rats |
title_full | Clavulanic acid improves ethanol withdrawal symptoms in rats |
title_fullStr | Clavulanic acid improves ethanol withdrawal symptoms in rats |
title_full_unstemmed | Clavulanic acid improves ethanol withdrawal symptoms in rats |
title_short | Clavulanic acid improves ethanol withdrawal symptoms in rats |
title_sort | clavulanic acid improves ethanol withdrawal symptoms in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351446/ https://www.ncbi.nlm.nih.gov/pubmed/32695288 http://dx.doi.org/10.22038/ijbms.2020.39129.9287 |
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