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Effects of omega-3 PUFA on the vitamin E and glutathione antioxidant defense system in individuals at ultra-high risk of psychosis.

Identifieur interne : 001E00 ( Main/Exploration ); précédent : 001D99; suivant : 001E01

Effects of omega-3 PUFA on the vitamin E and glutathione antioxidant defense system in individuals at ultra-high risk of psychosis.

Auteurs : Stefan Smesny [Allemagne] ; Berko Milleit [Allemagne] ; Miriam R. Schaefer [Australie] ; Uta-Christina Hipler [Allemagne] ; Christine Milleit [Allemagne] ; Cornelia Wiegand [Allemagne] ; Jana Hesse [Allemagne] ; Claudia M. Klier [Autriche] ; Magdalena Holub [Autriche] ; Ingrid Holzer [Autriche] ; Michael Berk [Australie] ; Patrick D. Mcgorry [Australie] ; Heinrich Sauer [Allemagne] ; G Paul Amminger [Australie]

Source :

RBID : pubmed:26260538

Descripteurs français

English descriptors

Abstract

BACKGROUND

Oxidative stress and impaired antioxidant defenses are reported in schizophrenia and are associated with disturbed neurodevelopment, brain structural alterations, glutamatergic imbalance, increased negative symptoms, and cognitive impairment. There is evidence that oxidative stress predates the onset of acute psychotic illness. Here, we investigate the effects of omega-3 PUFA on the vitamin E and glutathione antioxidant defense system (AODS).

METHOD

In 64 help-seeking UHR-individuals (13-25 years of age), vitamin E levels and glutathione were investigated before and after 12 weeks of treatment with either 1.2g/d omega-3 (PUFA-E) or saturated fatty acids (SFA-E), with each condition also containing 30.4mg/d alpha-tocopherol to ensure absorption without additional oxidative risk.

RESULTS

In multivariate tests, the effects on the AODS (alpha-tocopherol, total glutathione) were not significantly different (p=0.13, p=0.11, respectively) between treatment conditions. According to univariate findings, only PUFA-E caused a significant alpha-tocopherol increase, while PUFA-E and SFA-E caused a significant gamma- and delta-tocopherol decrease. Total glutathione (GSHt) was decreased by PUFA-E supplementation.

CONCLUSION

Effects of the PUFA-E condition on the vitamin E and glutathione AODS could be mechanisms underlying its clinical effectiveness. In terms of the vitamin E protection system, PUFA-E seems to directly support the antioxidative defense at membrane level. The effect of PUFA-E on GSHt is not yet fully understood, but could reflect antioxidative effects, resulting in decreased demand for glutathione. It is still necessary to further clarify which type of PUFA/antioxidant combination, and in which dose, is effective at each stage of psychotic illness.


DOI: 10.1016/j.plefa.2015.07.001
PubMed: 26260538


Affiliations:


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Le document en format XML

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<name sortKey="Sauer, Heinrich" sort="Sauer, Heinrich" uniqKey="Sauer H" first="Heinrich" last="Sauer">Heinrich Sauer</name>
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<name sortKey="Amminger, G Paul" sort="Amminger, G Paul" uniqKey="Amminger G" first="G Paul" last="Amminger">G Paul Amminger</name>
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<nlm:affiliation>Department of Child and Adolescent Psychiatry, Medical University Vienna, Währingergürtel 18-20, A-1090 Vienna, Austria; Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia.</nlm:affiliation>
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<nlm:affiliation>Department of Psychiatry, University Hospital Jena, Philosophenweg 3, D-07743 Jena, Germany; Department of Psychiatry and Psychotherapy, Thueringen-Kliniken GmbH, Rainweg 68, 07318 Saalfeld/Saale, Germany.</nlm:affiliation>
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<name sortKey="Schaefer, Miriam R" sort="Schaefer, Miriam R" uniqKey="Schaefer M" first="Miriam R" last="Schaefer">Miriam R. Schaefer</name>
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<nlm:affiliation>Department of Child and Adolescent Psychiatry, Medical University Vienna, Währingergürtel 18-20, A-1090 Vienna, Austria; Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
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<name sortKey="Hipler, Uta Christina" sort="Hipler, Uta Christina" uniqKey="Hipler U" first="Uta-Christina" last="Hipler">Uta-Christina Hipler</name>
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<name sortKey="Wiegand, Cornelia" sort="Wiegand, Cornelia" uniqKey="Wiegand C" first="Cornelia" last="Wiegand">Cornelia Wiegand</name>
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<name sortKey="Hesse, Jana" sort="Hesse, Jana" uniqKey="Hesse J" first="Jana" last="Hesse">Jana Hesse</name>
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<name sortKey="Klier, Claudia M" sort="Klier, Claudia M" uniqKey="Klier C" first="Claudia M" last="Klier">Claudia M. Klier</name>
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<name sortKey="Holub, Magdalena" sort="Holub, Magdalena" uniqKey="Holub M" first="Magdalena" last="Holub">Magdalena Holub</name>
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<name sortKey="Holzer, Ingrid" sort="Holzer, Ingrid" uniqKey="Holzer I" first="Ingrid" last="Holzer">Ingrid Holzer</name>
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<nlm:affiliation>Department of Nutritional Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.</nlm:affiliation>
<country xml:lang="fr">Autriche</country>
<wicri:regionArea>Department of Nutritional Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna</wicri:regionArea>
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<name sortKey="Berk, Michael" sort="Berk, Michael" uniqKey="Berk M" first="Michael" last="Berk">Michael Berk</name>
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<nlm:affiliation>Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia; IMPACT Strategic Research Centre, Deakin University of Melbourne, School of Medicine, Barwon Health, Geelong, Australia; Florey Institute for Neuroscience and Mental Health, Parkville, Australia; Department of Psychiatry, The University of Melbourne, Royal Parade, Parkville, Melbourne 3052, Victoria, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia; IMPACT Strategic Research Centre, Deakin University of Melbourne, School of Medicine, Barwon Health, Geelong, Australia; Florey Institute for Neuroscience and Mental Health, Parkville, Australia; Department of Psychiatry, The University of Melbourne, Royal Parade, Parkville, Melbourne 3052, Victoria</wicri:regionArea>
<orgName type="university">Université de Melbourne</orgName>
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<settlement type="city">Melbourne</settlement>
<region type="état">Victoria (État)</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Mcgorry, Patrick D" sort="Mcgorry, Patrick D" uniqKey="Mcgorry P" first="Patrick D" last="Mcgorry">Patrick D. Mcgorry</name>
<affiliation wicri:level="4">
<nlm:affiliation>Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria</wicri:regionArea>
<orgName type="university">Université de Melbourne</orgName>
<placeName>
<settlement type="city">Melbourne</settlement>
<region type="état">Victoria (État)</region>
</placeName>
</affiliation>
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<author>
<name sortKey="Sauer, Heinrich" sort="Sauer, Heinrich" uniqKey="Sauer H" first="Heinrich" last="Sauer">Heinrich Sauer</name>
<affiliation wicri:level="1">
<nlm:affiliation>Department of Psychiatry, University Hospital Jena, Philosophenweg 3, D-07743 Jena, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
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<author>
<name sortKey="Amminger, G Paul" sort="Amminger, G Paul" uniqKey="Amminger G" first="G Paul" last="Amminger">G Paul Amminger</name>
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<nlm:affiliation>Department of Child and Adolescent Psychiatry, Medical University Vienna, Währingergürtel 18-20, A-1090 Vienna, Austria; Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Child and Adolescent Psychiatry, Medical University Vienna, Währingergürtel 18-20, A-1090 Vienna, Austria; Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria</wicri:regionArea>
<wicri:noRegion>Victoria</wicri:noRegion>
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<series>
<title level="j">Prostaglandins, leukotrienes, and essential fatty acids</title>
<idno type="eISSN">1532-2823</idno>
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<date when="2015" type="published">2015</date>
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<term>Adolescent (MeSH)</term>
<term>Adult (MeSH)</term>
<term>Antioxidants (administration & dosage)</term>
<term>Antioxidants (analysis)</term>
<term>Cross-Sectional Studies (MeSH)</term>
<term>Fatty Acids (administration & dosage)</term>
<term>Fatty Acids (pharmacology)</term>
<term>Fatty Acids, Omega-3 (administration & dosage)</term>
<term>Fatty Acids, Omega-3 (pharmacology)</term>
<term>Female (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Longitudinal Studies (MeSH)</term>
<term>Male (MeSH)</term>
<term>Multivariate Analysis (MeSH)</term>
<term>Psychotic Disorders (drug therapy)</term>
<term>Treatment Outcome (MeSH)</term>
<term>Vitamin E (administration & dosage)</term>
<term>Vitamin E (analysis)</term>
<term>Young Adult (MeSH)</term>
<term>alpha-Tocopherol (administration & dosage)</term>
<term>alpha-Tocopherol (analysis)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Acides gras (administration et posologie)</term>
<term>Acides gras (pharmacologie)</term>
<term>Acides gras omega-3 (administration et posologie)</term>
<term>Acides gras omega-3 (pharmacologie)</term>
<term>Adolescent (MeSH)</term>
<term>Adulte (MeSH)</term>
<term>Analyse multifactorielle (MeSH)</term>
<term>Antioxydants (administration et posologie)</term>
<term>Antioxydants (analyse)</term>
<term>Femelle (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Jeune adulte (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Résultat thérapeutique (MeSH)</term>
<term>Troubles psychotiques (traitement médicamenteux)</term>
<term>Vitamine E (administration et posologie)</term>
<term>Vitamine E (analyse)</term>
<term>alpha-Tocophérol (administration et posologie)</term>
<term>alpha-Tocophérol (analyse)</term>
<term>Études longitudinales (MeSH)</term>
<term>Études transversales (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en">
<term>Antioxidants</term>
<term>Fatty Acids</term>
<term>Fatty Acids, Omega-3</term>
<term>Vitamin E</term>
<term>alpha-Tocopherol</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en">
<term>Antioxidants</term>
<term>Vitamin E</term>
<term>alpha-Tocopherol</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Fatty Acids</term>
<term>Fatty Acids, Omega-3</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr">
<term>Acides gras</term>
<term>Acides gras omega-3</term>
<term>Antioxydants</term>
<term>Vitamine E</term>
<term>alpha-Tocophérol</term>
</keywords>
<keywords scheme="MESH" qualifier="analyse" xml:lang="fr">
<term>Antioxydants</term>
<term>Vitamine E</term>
<term>alpha-Tocophérol</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Psychotic Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Acides gras</term>
<term>Acides gras omega-3</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Troubles psychotiques</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adolescent</term>
<term>Adult</term>
<term>Cross-Sectional Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Longitudinal Studies</term>
<term>Male</term>
<term>Multivariate Analysis</term>
<term>Treatment Outcome</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adolescent</term>
<term>Adulte</term>
<term>Analyse multifactorielle</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Mâle</term>
<term>Résultat thérapeutique</term>
<term>Études longitudinales</term>
<term>Études transversales</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>Oxidative stress and impaired antioxidant defenses are reported in schizophrenia and are associated with disturbed neurodevelopment, brain structural alterations, glutamatergic imbalance, increased negative symptoms, and cognitive impairment. There is evidence that oxidative stress predates the onset of acute psychotic illness. Here, we investigate the effects of omega-3 PUFA on the vitamin E and glutathione antioxidant defense system (AODS).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHOD</b>
</p>
<p>In 64 help-seeking UHR-individuals (13-25 years of age), vitamin E levels and glutathione were investigated before and after 12 weeks of treatment with either 1.2g/d omega-3 (PUFA-E) or saturated fatty acids (SFA-E), with each condition also containing 30.4mg/d alpha-tocopherol to ensure absorption without additional oxidative risk.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>In multivariate tests, the effects on the AODS (alpha-tocopherol, total glutathione) were not significantly different (p=0.13, p=0.11, respectively) between treatment conditions. According to univariate findings, only PUFA-E caused a significant alpha-tocopherol increase, while PUFA-E and SFA-E caused a significant gamma- and delta-tocopherol decrease. Total glutathione (GSHt) was decreased by PUFA-E supplementation.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>Effects of the PUFA-E condition on the vitamin E and glutathione AODS could be mechanisms underlying its clinical effectiveness. In terms of the vitamin E protection system, PUFA-E seems to directly support the antioxidative defense at membrane level. The effect of PUFA-E on GSHt is not yet fully understood, but could reflect antioxidative effects, resulting in decreased demand for glutathione. It is still necessary to further clarify which type of PUFA/antioxidant combination, and in which dose, is effective at each stage of psychotic illness.</p>
</div>
</front>
</TEI>
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<DateCompleted>
<Year>2016</Year>
<Month>06</Month>
<Day>09</Day>
</DateCompleted>
<DateRevised>
<Year>2015</Year>
<Month>09</Month>
<Day>24</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1532-2823</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>101</Volume>
<PubDate>
<Year>2015</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>Prostaglandins, leukotrienes, and essential fatty acids</Title>
<ISOAbbreviation>Prostaglandins Leukot Essent Fatty Acids</ISOAbbreviation>
</Journal>
<ArticleTitle>Effects of omega-3 PUFA on the vitamin E and glutathione antioxidant defense system in individuals at ultra-high risk of psychosis.</ArticleTitle>
<Pagination>
<MedlinePgn>15-21</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.plefa.2015.07.001</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">S0952-3278(15)00135-0</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Oxidative stress and impaired antioxidant defenses are reported in schizophrenia and are associated with disturbed neurodevelopment, brain structural alterations, glutamatergic imbalance, increased negative symptoms, and cognitive impairment. There is evidence that oxidative stress predates the onset of acute psychotic illness. Here, we investigate the effects of omega-3 PUFA on the vitamin E and glutathione antioxidant defense system (AODS).</AbstractText>
<AbstractText Label="METHOD" NlmCategory="METHODS">In 64 help-seeking UHR-individuals (13-25 years of age), vitamin E levels and glutathione were investigated before and after 12 weeks of treatment with either 1.2g/d omega-3 (PUFA-E) or saturated fatty acids (SFA-E), with each condition also containing 30.4mg/d alpha-tocopherol to ensure absorption without additional oxidative risk.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">In multivariate tests, the effects on the AODS (alpha-tocopherol, total glutathione) were not significantly different (p=0.13, p=0.11, respectively) between treatment conditions. According to univariate findings, only PUFA-E caused a significant alpha-tocopherol increase, while PUFA-E and SFA-E caused a significant gamma- and delta-tocopherol decrease. Total glutathione (GSHt) was decreased by PUFA-E supplementation.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Effects of the PUFA-E condition on the vitamin E and glutathione AODS could be mechanisms underlying its clinical effectiveness. In terms of the vitamin E protection system, PUFA-E seems to directly support the antioxidative defense at membrane level. The effect of PUFA-E on GSHt is not yet fully understood, but could reflect antioxidative effects, resulting in decreased demand for glutathione. It is still necessary to further clarify which type of PUFA/antioxidant combination, and in which dose, is effective at each stage of psychotic illness.</AbstractText>
<CopyrightInformation>Copyright © 2015 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
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<LastName>Smesny</LastName>
<ForeName>Stefan</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Department of Psychiatry, University Hospital Jena, Philosophenweg 3, D-07743 Jena, Germany. Electronic address: stefan.smesny@med.uni-jena.de.</Affiliation>
</AffiliationInfo>
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<LastName>Milleit</LastName>
<ForeName>Berko</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Department of Psychiatry, University Hospital Jena, Philosophenweg 3, D-07743 Jena, Germany; Department of Psychiatry and Psychotherapy, Thueringen-Kliniken GmbH, Rainweg 68, 07318 Saalfeld/Saale, Germany.</Affiliation>
</AffiliationInfo>
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<ForeName>Miriam R</ForeName>
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<ForeName>Uta-Christina</ForeName>
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<Affiliation>Department of Dermatology, University Hospital Jena, Erfurter Straße 35, D-07743 Jena, Germany.</Affiliation>
</AffiliationInfo>
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<LastName>Milleit</LastName>
<ForeName>Christine</ForeName>
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<Affiliation>Department of Psychiatry, University Hospital Jena, Philosophenweg 3, D-07743 Jena, Germany; Department of Dermatology, University Hospital Jena, Erfurter Straße 35, D-07743 Jena, Germany.</Affiliation>
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<LastName>Wiegand</LastName>
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<Affiliation>Department of Dermatology, University Hospital Jena, Erfurter Straße 35, D-07743 Jena, Germany.</Affiliation>
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<LastName>Hesse</LastName>
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</AffiliationInfo>
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<Affiliation>Department of Nutritional Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.</Affiliation>
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<LastName>Holzer</LastName>
<ForeName>Ingrid</ForeName>
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<Affiliation>Department of Nutritional Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria.</Affiliation>
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<LastName>Berk</LastName>
<ForeName>Michael</ForeName>
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<Affiliation>Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia; IMPACT Strategic Research Centre, Deakin University of Melbourne, School of Medicine, Barwon Health, Geelong, Australia; Florey Institute for Neuroscience and Mental Health, Parkville, Australia; Department of Psychiatry, The University of Melbourne, Royal Parade, Parkville, Melbourne 3052, Victoria, Australia.</Affiliation>
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<Affiliation>Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia.</Affiliation>
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<Author ValidYN="Y">
<LastName>Sauer</LastName>
<ForeName>Heinrich</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Psychiatry, University Hospital Jena, Philosophenweg 3, D-07743 Jena, Germany.</Affiliation>
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<LastName>Amminger</LastName>
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<Affiliation>Department of Child and Adolescent Psychiatry, Medical University Vienna, Währingergürtel 18-20, A-1090 Vienna, Austria; Orygen, The National Centre of Excellence in Youth Mental Health and Orygen Youth Health Research Centre, The University of Melbourne, Locked Bag 10, 35 Poplar Road Parkville, Melbourne 3052, Victoria, Australia.</Affiliation>
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<Keyword MajorTopicYN="N">Follow-up</Keyword>
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<name sortKey="Holub, Magdalena" sort="Holub, Magdalena" uniqKey="Holub M" first="Magdalena" last="Holub">Magdalena Holub</name>
<name sortKey="Holzer, Ingrid" sort="Holzer, Ingrid" uniqKey="Holzer I" first="Ingrid" last="Holzer">Ingrid Holzer</name>
</country>
</tree>
</affiliations>
</record>

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