Linking Oxidative Stress and Proteinopathy in Alzheimer’s Disease

Proteinopathy and excessive production of reactive oxygen species (ROS), which are the principal features observed in the Alzheimer’s disease (AD) brain, contribute to neuronal toxicity. β-amyloid and tau are the primary proteins responsible for the proteinopathy (amyloidopathy and tauopathy, respec...

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Main Authors: Chanchal Sharma, Sang Ryong Kim
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Antioxidants
Subjects:
Online Access:https://www.mdpi.com/2076-3921/10/8/1231
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author Chanchal Sharma
Sang Ryong Kim
author_facet Chanchal Sharma
Sang Ryong Kim
author_sort Chanchal Sharma
collection DOAJ
description Proteinopathy and excessive production of reactive oxygen species (ROS), which are the principal features observed in the Alzheimer’s disease (AD) brain, contribute to neuronal toxicity. β-amyloid and tau are the primary proteins responsible for the proteinopathy (amyloidopathy and tauopathy, respectively) in AD, which depends on ROS production; these aggregates can also generate ROS. These mechanisms work in concert and reinforce each other to drive the pathology observed in the aging brain, which primarily involves oxidative stress (OS). This, in turn, triggers neurodegeneration due to the subsequent loss of synapses and neurons. Understanding these interactions may thus aid in the identification of potential neuroprotective therapies that could be clinically useful. Here, we review the role of β-amyloid and tau in the activation of ROS production. We then further discuss how free radicals can influence structural changes in key toxic intermediates and describe the putative mechanisms by which OS and oligomers cause neuronal death.
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spelling doaj.art-a7baa429a7ad4216b400aa367c156b4b2023-11-22T06:36:03ZengMDPI AGAntioxidants2076-39212021-07-01108123110.3390/antiox10081231Linking Oxidative Stress and Proteinopathy in Alzheimer’s DiseaseChanchal Sharma0Sang Ryong Kim1School of Life Sciences, Kyungpook National University, Daegu 41566, KoreaSchool of Life Sciences, Kyungpook National University, Daegu 41566, KoreaProteinopathy and excessive production of reactive oxygen species (ROS), which are the principal features observed in the Alzheimer’s disease (AD) brain, contribute to neuronal toxicity. β-amyloid and tau are the primary proteins responsible for the proteinopathy (amyloidopathy and tauopathy, respectively) in AD, which depends on ROS production; these aggregates can also generate ROS. These mechanisms work in concert and reinforce each other to drive the pathology observed in the aging brain, which primarily involves oxidative stress (OS). This, in turn, triggers neurodegeneration due to the subsequent loss of synapses and neurons. Understanding these interactions may thus aid in the identification of potential neuroprotective therapies that could be clinically useful. Here, we review the role of β-amyloid and tau in the activation of ROS production. We then further discuss how free radicals can influence structural changes in key toxic intermediates and describe the putative mechanisms by which OS and oligomers cause neuronal death.https://www.mdpi.com/2076-3921/10/8/1231proteinopathyreactive oxygen speciesAlzheimer’s diseaseamyloidopathytauopathyoxidative stress
spellingShingle Chanchal Sharma
Sang Ryong Kim
Linking Oxidative Stress and Proteinopathy in Alzheimer’s Disease
Antioxidants
proteinopathy
reactive oxygen species
Alzheimer’s disease
amyloidopathy
tauopathy
oxidative stress
title Linking Oxidative Stress and Proteinopathy in Alzheimer’s Disease
title_full Linking Oxidative Stress and Proteinopathy in Alzheimer’s Disease
title_fullStr Linking Oxidative Stress and Proteinopathy in Alzheimer’s Disease
title_full_unstemmed Linking Oxidative Stress and Proteinopathy in Alzheimer’s Disease
title_short Linking Oxidative Stress and Proteinopathy in Alzheimer’s Disease
title_sort linking oxidative stress and proteinopathy in alzheimer s disease
topic proteinopathy
reactive oxygen species
Alzheimer’s disease
amyloidopathy
tauopathy
oxidative stress
url https://www.mdpi.com/2076-3921/10/8/1231
work_keys_str_mv AT chanchalsharma linkingoxidativestressandproteinopathyinalzheimersdisease
AT sangryongkim linkingoxidativestressandproteinopathyinalzheimersdisease