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Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment

OBJECTIVE(S): Alzheimer’s disease (AD), the most common cause of dementia, is one of the leading causes of morbidity and death in the world. Currently, treatment mostly used to slow down the disease progression. Herbal remedies are considered by many in the community as a natural and safe treatment...

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Autores principales: Alihosseini, Tahereh, Azizi, Monireh, Abbasi, Nasser, Mohammadpour, Shahram, Bagheri, Maryam
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/PMC10311968/
https://www.ncbi.nlm.nih.gov/pubmed/37396937
http://dx.doi.org/10.22038/IJBMS.2023.66831.14665
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author Alihosseini, Tahereh
Azizi, Monireh
Abbasi, Nasser
Mohammadpour, Shahram
Bagheri, Maryam
author_facet Alihosseini, Tahereh
Azizi, Monireh
Abbasi, Nasser
Mohammadpour, Shahram
Bagheri, Maryam
author_sort Alihosseini, Tahereh
collection PubMed
description OBJECTIVE(S): Alzheimer’s disease (AD), the most common cause of dementia, is one of the leading causes of morbidity and death in the world. Currently, treatment mostly used to slow down the disease progression. Herbal remedies are considered by many in the community as a natural and safe treatment with fewer side effects. Silibinin, the active ingredient of Silybum marionum, has anti-oxidant, neurotrophic and neuroprotective characteristics. Therefore, here, the effect of different doses of Silibinin extract on oxidative stress and expression of neurotrophic factors was investigated. MATERIALS AND METHODS: Forty eight male Wistar rats were randomly divided into sham, lesion; Aβ(1-40) injection, lesion-treatment; Aβ(1-40) injection followed by different doses of silibinin (50, 100, 200 mg / kg) through gavage and lesion-vehicle group; Aβ(1-40) injection + vehicle of silibinin. Morris water Maze (MWM) was done 28 days after the last treatment. Hippocampal tissue was removed for biochemical analysis. Production of nitric oxide (NO) and reactive oxygen species (ROS), expression of BDNF/VEGF and cell viability were measured using Griess, fluorimetry, Western blotting and MTT techniques. RESULTS: Different concentrations of silibinin improved behavioral performance in animals. Higher doses of Silibinin could improve memory and learning function through MWM. Also, increasing the concentration of silibinin resulted in decreased ROS and NO production in a dose-dependent manner. CONCLUSION: Consequently, silibinin may act as a potential candidate for alleviating symptoms of AD.
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spelling pubmed-103119682023-07-01 Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment Alihosseini, Tahereh Azizi, Monireh Abbasi, Nasser Mohammadpour, Shahram Bagheri, Maryam Iran J Basic Med Sci Original Article OBJECTIVE(S): Alzheimer’s disease (AD), the most common cause of dementia, is one of the leading causes of morbidity and death in the world. Currently, treatment mostly used to slow down the disease progression. Herbal remedies are considered by many in the community as a natural and safe treatment with fewer side effects. Silibinin, the active ingredient of Silybum marionum, has anti-oxidant, neurotrophic and neuroprotective characteristics. Therefore, here, the effect of different doses of Silibinin extract on oxidative stress and expression of neurotrophic factors was investigated. MATERIALS AND METHODS: Forty eight male Wistar rats were randomly divided into sham, lesion; Aβ(1-40) injection, lesion-treatment; Aβ(1-40) injection followed by different doses of silibinin (50, 100, 200 mg / kg) through gavage and lesion-vehicle group; Aβ(1-40) injection + vehicle of silibinin. Morris water Maze (MWM) was done 28 days after the last treatment. Hippocampal tissue was removed for biochemical analysis. Production of nitric oxide (NO) and reactive oxygen species (ROS), expression of BDNF/VEGF and cell viability were measured using Griess, fluorimetry, Western blotting and MTT techniques. RESULTS: Different concentrations of silibinin improved behavioral performance in animals. Higher doses of Silibinin could improve memory and learning function through MWM. Also, increasing the concentration of silibinin resulted in decreased ROS and NO production in a dose-dependent manner. CONCLUSION: Consequently, silibinin may act as a potential candidate for alleviating symptoms of AD. Mashhad University of Medical Sciences 2023 /pmc/articles/PMC10311968/ /pubmed/37396937 http://dx.doi.org/10.22038/IJBMS.2023.66831.14665 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 Article
Alihosseini, Tahereh
Azizi, Monireh
Abbasi, Nasser
Mohammadpour, Shahram
Bagheri, Maryam
Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment
title Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment
title_full Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment
title_fullStr Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment
title_full_unstemmed Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment
title_short Amelioration of amyloid beta (Aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment
title_sort amelioration of amyloid beta (aβ(1-40)) neurotoxicity by administration of silibinin; a behavioral and biochemical assessment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311968/
https://www.ncbi.nlm.nih.gov/pubmed/37396937
http://dx.doi.org/10.22038/IJBMS.2023.66831.14665
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