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      Neuroprotective Effects of Chronic Resveratrol Treatment and Exercise Training in the 3xTg-AD Mouse Model of Alzheimer’s Disease

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          Abstract

          To date, there is no cure or effective treatment for Alzheimer’s disease (AD), a chronic neurodegenerative condition that affects memory, language, and behavior. AD is characterized by neuroinflammation, accumulation of brain amyloid-beta (Aβ) oligomers and neurofibrillary tangles, increased neuronal apoptosis, and loss of synaptic function. Promoting regular exercise and a diet containing polyphenols are effective non-pharmacological approaches that prevent the progression of neurodegenerative diseases. In this study, we measured various conformational toxic species of Aβ and markers of inflammation, apoptosis, endolysosomal degradation, and neuroprotection after 5 months of exercise training (ET), resveratrol (Resv) treatment, or combination treatment in the 3xTg-AD mouse model of AD. Our main results indicate that Resv decreased neuroinflammation and accumulation of Aβ oligomers, increased levels of neurotrophins, synaptic markers, silent information regulator, and decreased markers of apoptosis, autophagy, endolysosomal degradation and ubiquitination in the brains of 3xTg-AD mice. ET improved some markers related to neuroprotection, but when combined with Resv treatment, the benefits achieved were as effective as Resv treatment alone. Our results show that the neuroprotective effects of Resv, ET or Resv and ET are associated with reduced toxicity of Aβ oligomers, suppression of neuronal autophagy, decreased apoptosis, and upregulation of key growth-related proteins.

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          Most cited references105

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          The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics.

          It has been more than 10 years since it was first proposed that the neurodegeneration in Alzheimer's disease (AD) may be caused by deposition of amyloid beta-peptide (Abeta) in plaques in brain tissue. According to the amyloid hypothesis, accumulation of Abeta in the brain is the primary influence driving AD pathogenesis. The rest of the disease process, including formation of neurofibrillary tangles containing tau protein, is proposed to result from an imbalance between Abeta production and Abeta clearance.
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            Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis.

            Soluble oligomers are common to most amyloids and may represent the primary toxic species of amyloids, like the Abeta peptide in Alzheimer's disease (AD). Here we show that all of the soluble oligomers tested display a common conformation-dependent structure that is unique to soluble oligomers regardless of sequence. The in vitro toxicity of soluble oligomers is inhibited by oligomer-specific antibody. Soluble oligomers have a unique distribution in human AD brain that is distinct from fibrillar amyloid. These results indicate that different types of soluble amyloid oligomers have a common structure and suggest they share a common mechanism of toxicity.
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              Alzheimer's disease is a synaptic failure.

              D. Selkoe (2002)
              In its earliest clinical phase, Alzheimer's disease characteristically produces a remarkably pure impairment of memory. Mounting evidence suggests that this syndrome begins with subtle alterations of hippocampal synaptic efficacy prior to frank neuronal degeneration, and that the synaptic dysfunction is caused by diffusible oligomeric assemblies of the amyloid beta protein.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                04 October 2020
                October 2020
                : 21
                : 19
                : 7337
                Affiliations
                [1 ]Department of Physiology, College of Graduate Studies, Midwestern University, Glendale, AZ 85308, USA; lalnak@ 123456midwestern.edu
                [2 ]Laboratory of Diabetes and Exercise Metabolism, College of Graduate Studies, Midwestern University, Glendale, AZ 85308, USA; manderson92@ 123456midwestern.edu
                [3 ]Department of Nutrition, Dietetics, and Hospitality Management, Auburn University, Auburn, AL 36849, USA; suhailrasool@ 123456hotmail.com (S.R.); rzl0050@ 123456auburn.edu (R.L.); yzz0088@ 123456auburn.edu (Y.Z.); thangge@ 123456auburn.edu (T.G.)
                [4 ]Department of Medical Education, University of Central Florida, College of Medicine, 6850 Lake Nona Blvd, Orlando, FL 32827, USA; Jeffrey.Plochocki@ 123456ucf.edu
                Author notes
                [* ]Correspondence: tbrode@ 123456midwestern.edu (T.L.B.); jeganrb@ 123456auburn.edu (J.R.B.)
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0001-9309-6213
                https://orcid.org/0000-0002-9054-2078
                https://orcid.org/0000-0001-6358-0012
                Article
                ijms-21-07337
                10.3390/ijms21197337
                7582460
                33020412
                36334480-0e67-4ea7-b420-7e1f2a5f0309
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 20 August 2020
                : 24 September 2020
                Categories
                Article

                Molecular biology
                alzheimer’s disease,exercise,resveratrol,brain,neuroinflammation,amyloid-beta,apoptosis,neurotrophin,autophagy

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