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The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats

OBJECTIVE: The present study examined the effects of Artemisia absinthium L. on scopolamine-induced memory dysfunction and brain tissue oxidative damage in rats. MATERIALS AND METHODS: Fifty rats were used in five groups: Control: received dimethyl sulfoxide (DMSO)/saline, Scopolamine: scopolamine (...

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Autores principales: Rahimi, Marzieh, Marefati, Narges, Beheshti, Farimah, Ahmadabady, Somaieh, Rakhshandeh, Hassan, Hosseini, Mahmoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840781/
https://www.ncbi.nlm.nih.gov/pubmed/36698740
http://dx.doi.org/10.22038/AJP.2022.62851.2991
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author Rahimi, Marzieh
Marefati, Narges
Beheshti, Farimah
Ahmadabady, Somaieh
Rakhshandeh, Hassan
Hosseini, Mahmoud
author_facet Rahimi, Marzieh
Marefati, Narges
Beheshti, Farimah
Ahmadabady, Somaieh
Rakhshandeh, Hassan
Hosseini, Mahmoud
author_sort Rahimi, Marzieh
collection PubMed
description OBJECTIVE: The present study examined the effects of Artemisia absinthium L. on scopolamine-induced memory dysfunction and brain tissue oxidative damage in rats. MATERIALS AND METHODS: Fifty rats were used in five groups: Control: received dimethyl sulfoxide (DMSO)/saline, Scopolamine: scopolamine (2 mg/kg) was administered along with DMSO/saline, and Scopolamine-Ext 50, Scopolamine-Ext 100, and Scopolamine-Ext 200 groups: A. absinthium hydroalcoholic extract 50, 100 and 200 mg/kg were administered before scopolamine. The Morris water maze (MWM) and passive avoidance (PA) tasks were used for assessment of behavioral parameters. Malondialdehyde (MDA), nitric oxide (NO) metabolites, total thiol, catalase (CAT), and superoxide dismutase (SOD) were measured in the cortex and hippocampus. RESULTS: A. absinthium decreased the delay time and distance traveled to reach the platform in the MWM test (p<0.05-p<0.001). Besides, the extract increased the delay time to pass in the dark and the light time while decreasing the number of entrances and the dark time in the PA task (p<0.05-p<0.001). In biochemical assessments, A. absinthium attenuated NO metabolites (p<0.001) and MDA (p<0.05- p<0.001) while enhanced total thiol (p<0.001), CAT and SOD (both p<0.05-p<0.001). CONCLUSION: This study revealed that A. absinthium improved memory and learning impairment and brain tissue oxidative damage in scopolamine-treated rats.
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spelling pubmed-98407812023-01-24 The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats Rahimi, Marzieh Marefati, Narges Beheshti, Farimah Ahmadabady, Somaieh Rakhshandeh, Hassan Hosseini, Mahmoud Avicenna J Phytomed Original Research Article OBJECTIVE: The present study examined the effects of Artemisia absinthium L. on scopolamine-induced memory dysfunction and brain tissue oxidative damage in rats. MATERIALS AND METHODS: Fifty rats were used in five groups: Control: received dimethyl sulfoxide (DMSO)/saline, Scopolamine: scopolamine (2 mg/kg) was administered along with DMSO/saline, and Scopolamine-Ext 50, Scopolamine-Ext 100, and Scopolamine-Ext 200 groups: A. absinthium hydroalcoholic extract 50, 100 and 200 mg/kg were administered before scopolamine. The Morris water maze (MWM) and passive avoidance (PA) tasks were used for assessment of behavioral parameters. Malondialdehyde (MDA), nitric oxide (NO) metabolites, total thiol, catalase (CAT), and superoxide dismutase (SOD) were measured in the cortex and hippocampus. RESULTS: A. absinthium decreased the delay time and distance traveled to reach the platform in the MWM test (p<0.05-p<0.001). Besides, the extract increased the delay time to pass in the dark and the light time while decreasing the number of entrances and the dark time in the PA task (p<0.05-p<0.001). In biochemical assessments, A. absinthium attenuated NO metabolites (p<0.001) and MDA (p<0.05- p<0.001) while enhanced total thiol (p<0.001), CAT and SOD (both p<0.05-p<0.001). CONCLUSION: This study revealed that A. absinthium improved memory and learning impairment and brain tissue oxidative damage in scopolamine-treated rats. Mashhad University of Medical Sciences 2023 /pmc/articles/PMC9840781/ /pubmed/36698740 http://dx.doi.org/10.22038/AJP.2022.62851.2991 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Rahimi, Marzieh
Marefati, Narges
Beheshti, Farimah
Ahmadabady, Somaieh
Rakhshandeh, Hassan
Hosseini, Mahmoud
The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats
title The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats
title_full The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats
title_fullStr The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats
title_full_unstemmed The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats
title_short The effects of Artemisia absinthium L. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats
title_sort effects of artemisia absinthium l. on scopolamine-induced learning and memory impairment and brain tissue oxidative damage in adult rats
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9840781/
https://www.ncbi.nlm.nih.gov/pubmed/36698740
http://dx.doi.org/10.22038/AJP.2022.62851.2991
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