Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer Disease

Background: Alzheimer disease is a progressive neurodegenerative disease, affecting a very high proportion of the aging population. Several studies have demonstrated that one of the main contributors to this disease is oxidative stress (OS), which causes peroxidation of protein, lipids, and DNA resu...

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Main Authors: Abir Abdullah Alamro, Ebtesam Atiah Alsulami, Moudhi Almutlaq, Amani Alghamedi, Majed Alokail, Samina Hyder Haq
Format: Article
Language:English
Published: SAGE Publishing 2020-05-01
Series:Journal of Central Nervous System Disease
Online Access:https://doi.org/10.1177/1179573520924311
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spelling doaj-e5ac6cf58f7749f6bcd866f4c6decdd52020-11-25T03:36:29ZengSAGE PublishingJournal of Central Nervous System Disease1179-57352020-05-011210.1177/1179573520924311Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer DiseaseAbir Abdullah AlamroEbtesam Atiah AlsulamiMoudhi AlmutlaqAmani AlghamediMajed AlokailSamina Hyder HaqBackground: Alzheimer disease is a progressive neurodegenerative disease, affecting a very high proportion of the aging population. Several studies have demonstrated that one of the main contributors to this disease is oxidative stress (OS), which causes peroxidation of protein, lipids, and DNA resulting in the formation of advanced glycosylated end products (AGE) in the brain tissues. These AGE are usually associated with the amyloid β (Aβ), which could further aggravate its toxicity and its clearance. Antioxidants counteract the deterioration caused by OS. Objective: We aimed to evaluate the effect of vitamin D3 and curcumin on primary cortical neuronal cultures exposed to Aβ 1-42 toxicity for different time periods. Methods: Primary cortical neuronal cultures were set up and exposed to Aβ 1-42 for up to 72 hours. Cell viability was studied by 3[4,5-dimethylthiazole-2-yl]-2,5-dipheyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assay. Biochemical assays for OS such as lipid peroxidation, reduced Glutathione(GSH), Glutathione S-transferase (GST), catalase, and superoxide dismutase (SOD) were conducted. Sandwich enzyme-linked immunosorbent assay (ELISA) was used to study the neurotrophic growth factor (NGF) expression. Results: Treatments with Aβ 1-42 caused an elevation in lipid peroxidation products, which were ameliorated in the presence of vitamin D3 and curcumin. Both enzymatic (GST, catalase, and SOD) and nonenzymatic antioxidants (reduced GSH) were raised significantly in the presence of vitamin D3 and curcumin, which resulted in the better recovery of neuronal cells from Aβ 1-42 treatment. Treatment with vitamin D3 and curcumin also resulted in the upregulation of NGF levels. Conclusions: This study suggests that vitamin D3 and curcumin can be a promising natural therapy for the treatment of Alzheimer disease.https://doi.org/10.1177/1179573520924311
collection DOAJ
language English
format Article
sources DOAJ
author Abir Abdullah Alamro
Ebtesam Atiah Alsulami
Moudhi Almutlaq
Amani Alghamedi
Majed Alokail
Samina Hyder Haq
spellingShingle Abir Abdullah Alamro
Ebtesam Atiah Alsulami
Moudhi Almutlaq
Amani Alghamedi
Majed Alokail
Samina Hyder Haq
Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer Disease
Journal of Central Nervous System Disease
author_facet Abir Abdullah Alamro
Ebtesam Atiah Alsulami
Moudhi Almutlaq
Amani Alghamedi
Majed Alokail
Samina Hyder Haq
author_sort Abir Abdullah Alamro
title Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer Disease
title_short Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer Disease
title_full Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer Disease
title_fullStr Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer Disease
title_full_unstemmed Therapeutic Potential of Vitamin D and Curcumin in an Model of Alzheimer Disease
title_sort therapeutic potential of vitamin d and curcumin in an model of alzheimer disease
publisher SAGE Publishing
series Journal of Central Nervous System Disease
issn 1179-5735
publishDate 2020-05-01
description Background: Alzheimer disease is a progressive neurodegenerative disease, affecting a very high proportion of the aging population. Several studies have demonstrated that one of the main contributors to this disease is oxidative stress (OS), which causes peroxidation of protein, lipids, and DNA resulting in the formation of advanced glycosylated end products (AGE) in the brain tissues. These AGE are usually associated with the amyloid β (Aβ), which could further aggravate its toxicity and its clearance. Antioxidants counteract the deterioration caused by OS. Objective: We aimed to evaluate the effect of vitamin D3 and curcumin on primary cortical neuronal cultures exposed to Aβ 1-42 toxicity for different time periods. Methods: Primary cortical neuronal cultures were set up and exposed to Aβ 1-42 for up to 72 hours. Cell viability was studied by 3[4,5-dimethylthiazole-2-yl]-2,5-dipheyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assay. Biochemical assays for OS such as lipid peroxidation, reduced Glutathione(GSH), Glutathione S-transferase (GST), catalase, and superoxide dismutase (SOD) were conducted. Sandwich enzyme-linked immunosorbent assay (ELISA) was used to study the neurotrophic growth factor (NGF) expression. Results: Treatments with Aβ 1-42 caused an elevation in lipid peroxidation products, which were ameliorated in the presence of vitamin D3 and curcumin. Both enzymatic (GST, catalase, and SOD) and nonenzymatic antioxidants (reduced GSH) were raised significantly in the presence of vitamin D3 and curcumin, which resulted in the better recovery of neuronal cells from Aβ 1-42 treatment. Treatment with vitamin D3 and curcumin also resulted in the upregulation of NGF levels. Conclusions: This study suggests that vitamin D3 and curcumin can be a promising natural therapy for the treatment of Alzheimer disease.
url https://doi.org/10.1177/1179573520924311
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