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The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats
BACKGROUND: Cognitive impairment is an unpleasant and progressive mental disorder characterized by learning and memory disabilities. Stress and alcohol are two known environmental factors that increase cognitive impairment. This study was designed to evaluate the relative role of cyclooxygenase 2 in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744420/ https://www.ncbi.nlm.nih.gov/pubmed/35071112 http://dx.doi.org/10.4103/abr.abr_287_20 |
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author | Hosseini-Sharifabad, Ali Alaei, Zahra Rabbani, Mohammad Seyedabadi, Mohammad |
author_facet | Hosseini-Sharifabad, Ali Alaei, Zahra Rabbani, Mohammad Seyedabadi, Mohammad |
author_sort | Hosseini-Sharifabad, Ali |
collection | PubMed |
description | BACKGROUND: Cognitive impairment is an unpleasant and progressive mental disorder characterized by learning and memory disabilities. Stress and alcohol are two known environmental factors that increase cognitive impairment. This study was designed to evaluate the relative role of cyclooxygenase 2 in alcohol or stress-induced cognitive impairment. MATERIALS AND METHODS: Male Wistar rats were randomly divided into groups with six rats in each. The groups included sham, control, alcohol (15% ethanol in drinking water), and restraint stress (restraint 6 h per day). Three separated groups received celecoxib at a dose of 20 mg/kg in addition to those listed above. The treatments continued daily for 28 days. The object recognition task (ORT) and Morris water maze (MWM) are used to evaluate the learning and memory. RESULTS: Alcohol or restrain stress significantly increased the time and distance needed to find the hidden platform in MWM. Furthermore, they decreased the recognition index in ORT compared to the control group. Administration of celecoxib significantly decreased the required time and traveled distance to reach the platform in alcohol-treated animals but not in the stress-exposed rats. Celecoxib also significantly increased the recognition index both in alcohol- or restraint stress-exposed animals. CONCLUSION: We found that either alcohol or restraint stress impairs memory in rats. In MWM, celecoxib improved the alcohol-induced memory impairment but could not show a reduction in memory deterioration due to restraint stress. In ORT, celecoxib reversed memory impairment due to both alcohol and restraint stress. |
format | Online Article Text |
id | pubmed-8744420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-87444202022-01-21 The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats Hosseini-Sharifabad, Ali Alaei, Zahra Rabbani, Mohammad Seyedabadi, Mohammad Adv Biomed Res Original Article BACKGROUND: Cognitive impairment is an unpleasant and progressive mental disorder characterized by learning and memory disabilities. Stress and alcohol are two known environmental factors that increase cognitive impairment. This study was designed to evaluate the relative role of cyclooxygenase 2 in alcohol or stress-induced cognitive impairment. MATERIALS AND METHODS: Male Wistar rats were randomly divided into groups with six rats in each. The groups included sham, control, alcohol (15% ethanol in drinking water), and restraint stress (restraint 6 h per day). Three separated groups received celecoxib at a dose of 20 mg/kg in addition to those listed above. The treatments continued daily for 28 days. The object recognition task (ORT) and Morris water maze (MWM) are used to evaluate the learning and memory. RESULTS: Alcohol or restrain stress significantly increased the time and distance needed to find the hidden platform in MWM. Furthermore, they decreased the recognition index in ORT compared to the control group. Administration of celecoxib significantly decreased the required time and traveled distance to reach the platform in alcohol-treated animals but not in the stress-exposed rats. Celecoxib also significantly increased the recognition index both in alcohol- or restraint stress-exposed animals. CONCLUSION: We found that either alcohol or restraint stress impairs memory in rats. In MWM, celecoxib improved the alcohol-induced memory impairment but could not show a reduction in memory deterioration due to restraint stress. In ORT, celecoxib reversed memory impairment due to both alcohol and restraint stress. Wolters Kluwer - Medknow 2021-11-26 /pmc/articles/PMC8744420/ /pubmed/35071112 http://dx.doi.org/10.4103/abr.abr_287_20 Text en Copyright: © 2021 Advanced Biomedical Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Hosseini-Sharifabad, Ali Alaei, Zahra Rabbani, Mohammad Seyedabadi, Mohammad The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats |
title | The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats |
title_full | The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats |
title_fullStr | The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats |
title_full_unstemmed | The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats |
title_short | The Role of Cyclooxygenase 2 in the Cognitive Impairment Induced by Alcohol or Stress in Rats |
title_sort | role of cyclooxygenase 2 in the cognitive impairment induced by alcohol or stress in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744420/ https://www.ncbi.nlm.nih.gov/pubmed/35071112 http://dx.doi.org/10.4103/abr.abr_287_20 |
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