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      Tocotrienol Affects Oxidative Stress, Cholesterol Homeostasis and the Amyloidogenic Pathway in Neuroblastoma Cells: Consequences for Alzheimer’s Disease

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          Abstract

          One of the characteristics of Alzheimer´s disease (AD) is an increased amyloid load and an enhanced level of reactive oxidative species (ROS). Vitamin E has known beneficial neuroprotective effects, and previously, some studies suggested that vitamin E is associated with a reduced risk of AD due to its antioxidative properties. However, epidemiological studies and nutritional approaches of vitamin E treatment are controversial. Here, we investigate the effect of α-tocotrienol, which belongs to the group of vitamin E, on AD-relevant processes in neuronal cell lines. In line with the literature, α-tocotrienol reduced the ROS level in SH-SY5Y cells. In the presence of tocotrienols, cholesterol and cholesterol esters, which have been shown to be risk factors in AD, were decreased. Besides the unambiguous positive effects of tocotrienol, amyloid-β (Aβ) levels were increased accompanied by an increase in the activity of enzymes responsible for Aβ production. Proteins and gene expression of the secretases and their components remained unchanged, whereas tocotrienol accelerates enzyme activity in cell-free assays. Besides enhanced Aβ production, tocotrienols inhibited Aβ degradation in neuro 2a (N2a)-cells. Our results might help to understand the controversial findings of vitamin E studies and demonstrate that besides the known positive neuroprotective properties, tocotrienols also have negative characteristics with respect to AD.

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          Most cited references71

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          Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families.

          The apolipoprotein E type 4 allele (APOE-epsilon 4) is genetically associated with the common late onset familial and sporadic forms of Alzheimer's disease (AD). Risk for AD increased from 20% to 90% and mean age at onset decreased from 84 to 68 years with increasing number of APOE-epsilon 4 alleles in 42 families with late onset AD. Thus APOE-epsilon 4 gene dose is a major risk factor for late onset AD and, in these families, homozygosity for APOE-epsilon 4 was virtually sufficient to cause AD by age 80.
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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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              Natural forms of vitamin E: metabolism, antioxidant, and anti-inflammatory activities and their role in disease prevention and therapy.

              Qing Jiang (2014)
              The vitamin E family consists of four tocopherols and four tocotrienols. α-Tocopherol (αT) is the predominant form of vitamin E in tissues and its deficiency leads to ataxia in humans. However, results from many clinical studies do not support a protective role of αT in disease prevention in people with adequate nutrient status. On the other hand, recent mechanistic studies indicate that other forms of vitamin E, such as γ-tocopherol (γT), δ-tocopherol, and γ-tocotrienol, have unique antioxidant and anti-inflammatory properties that are superior to those of αT in prevention and therapy against chronic diseases. These vitamin E forms scavenge reactive nitrogen species, inhibit cyclooxygenase- and 5-lipoxygenase-catalyzed eicosanoids, and suppress proinflammatory signaling such as NF-κB and STAT3/6. Unlike αT, other vitamin E forms are significantly metabolized to carboxychromanols via cytochrome P450-initiated side-chain ω-oxidation. Long-chain carboxychromanols, especially 13'-carboxychromanols, are shown to have stronger anti-inflammatory effects than unmetabolized vitamins and may therefore contribute to the beneficial effects of vitamin E forms in vivo. Consistent with mechanistic findings, animal and human studies show that γT and tocotrienols may be useful against inflammation-associated diseases. This review focuses on non-αT forms of vitamin E with respect to their metabolism, anti-inflammatory effects and mechanisms, and in vivo efficacy in preclinical models as well as human clinical intervention studies. Copyright © 2014 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Role: Academic Editor
                Role: Academic Editor
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                29 October 2016
                November 2016
                : 17
                : 11
                : 1809
                Affiliations
                [1 ]Experimental Neurology, Saarland University, Kirrberger Straße 1, 66421 Homburg/Saar, Germany; liesa.regner@ 123456uks.eu (L.R.); janine.mett@ 123456uks.eu (J.M.); christoph.stahlmann@ 123456uks.eu (C.P.S.); pascals91@ 123456gmail.com (P.S.); christophernelke@ 123456yahoo.de (C.N.); olga.streidenberger@ 123456uks.eu (O.S.); hannah.stoetzel@ 123456uks.eu (H.S.); Jakob.winkler@ 123456hotmail.de (J.W.); shatharamadhan@ 123456yahoo.com (S.R.Z.); andrea.thiel@ 123456uks.eu (A.T.); heike.grimm@ 123456uks.eu (H.S.G.); tobias.hartmann@ 123456mx.uni-saarland.de (T.H.)
                [2 ]Neurodegeneration and Neurobiology, Saarland University, Kirrberger Straße 1, 66421 Homburg/Saar, Germany
                [3 ]Deutsches Institut für DemenzPrävention (DIDP), Saarland University, Kirrberger Straße 1, 66421 Homburg/Saar, Germany
                [4 ]Institute of Bioanalytical Chemistry, Saarland University, 66123 Saarbrücken, Germany; dietrich.volmer@ 123456mx.uni-saarland.de
                [5 ]Department of Psychiatry and Psychotherapy, Clinical Research Group, University Medical Centre Johannes Gutenberg-University Mainz, Untere Zahlbacher Straße 8, 55131 Mainz, Germany; Kristina.Endres@ 123456unimedizin-mainz.de
                Author notes
                [* ]Correspondence: marcus.grimm@ 123456uks.eu ; Tel.: +49-6841-1647-919; Fax: +49-6841-1647-925
                [†]

                These authors contributed equally to this work.

                Article
                ijms-17-01809
                10.3390/ijms17111809
                5133810
                27801864
                b00f6696-e234-4fe5-9260-dfbd30d38bf6
                © 2016 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
                : 31 August 2016
                : 21 October 2016
                Categories
                Article

                Molecular biology
                tocotrienol,vitamin e,alzheimer´s disease,amyloid-β,tocopherol,aβ degradation,β-secretase,γ-secretase

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