Effects of Long-Term Treatment with a Blend of Highly Purified Olive Secoiridoids on Cognition and Brain ATP Levels in Aged NMRI Mice
Aging represents a major risk factor for developing neurodegenerative diseases such as Alzheimer’s disease (AD). As components of the Mediterranean diet, olive polyphenols may play a crucial role in the prevention of AD. Since mitochondrial dysfunction acts as a final pathway in both brain aging and...
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description | Aging represents a major risk factor for developing neurodegenerative diseases such as Alzheimer’s disease (AD). As components of the Mediterranean diet, olive polyphenols may play a crucial role in the prevention of AD. Since mitochondrial dysfunction acts as a final pathway in both brain aging and AD, respectively, the effects of a mixture of highly purified olive secoiridoids were tested on cognition and ATP levels in a commonly used mouse model for brain aging. Over 6 months, female NMRI mice (12 months of age) were fed with a blend containing highly purified olive secoiridoids (POS) including oleuropein, hydroxytyrosol and oleurosid standardized for 50 mg oleuropein/kg diet (equivalent to 13.75 mg POS/kg b.w.) or the study diet without POS as control. Mice aged 3 months served as young controls. Behavioral tests showed deficits in cognition in aged mice. Levels of ATP and mRNA levels of NADH-reductase, cytochrome-c-oxidase, and citrate synthase were significantly reduced in the brains of aged mice indicating mitochondrial dysfunction. Moreover, gene expression of Sirt1, CREB, Gap43, and GPx-1 was significantly reduced in the brain tissue of aged mice. POS-fed mice showed improved spatial working memory. Furthermore, POS restored brain ATP levels in aged mice which were significantly increased. Our results show that a diet rich in purified olive polyphenols has positive long-term effects on cognition and energy metabolism in the brain of aged mice. |
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As components of the Mediterranean diet, olive polyphenols may play a crucial role in the prevention of AD. Since mitochondrial dysfunction acts as a final pathway in both brain aging and AD, respectively, the effects of a mixture of highly purified olive secoiridoids were tested on cognition and ATP levels in a commonly used mouse model for brain aging. Over 6 months, female NMRI mice (12 months of age) were fed with a blend containing highly purified olive secoiridoids (POS) including oleuropein, hydroxytyrosol and oleurosid standardized for 50 mg oleuropein/kg diet (equivalent to 13.75 mg POS/kg b.w.) or the study diet without POS as control. Mice aged 3 months served as young controls. Behavioral tests showed deficits in cognition in aged mice. Levels of ATP and mRNA levels of NADH-reductase, cytochrome-c-oxidase, and citrate synthase were significantly reduced in the brains of aged mice indicating mitochondrial dysfunction. Moreover, gene expression of Sirt1, CREB, Gap43, and GPx-1 was significantly reduced in the brain tissue of aged mice. POS-fed mice showed improved spatial working memory. Furthermore, POS restored brain ATP levels in aged mice which were significantly increased. Our results show that a diet rich in purified olive polyphenols has positive long-term effects on cognition and energy metabolism in the brain of aged mice.</description><identifier>ISSN: 1942-0900</identifier><identifier>EISSN: 1942-0994</identifier><identifier>DOI: 10.1155/2018/4070935</identifier><identifier>PMID: 30510619</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Adenosine Triphosphate - metabolism ; Advertising executives ; Aging ; Aging - drug effects ; Aging - metabolism ; Alzheimer's disease ; Analysis ; Animal cognition ; Animals ; Biosynthesis ; Brain - drug effects ; Brain - metabolism ; Brain research ; Cognition ; Cognition - drug effects ; Diet ; Disease ; Disease Models, Animal ; Fatty acids ; Female ; Gene expression ; Humans ; Iridoids - pharmacology ; Laboratory animals ; Magnetic resonance imaging ; Mice ; Nervous system diseases ; Neuroblastoma - drug therapy ; Neuroblastoma - metabolism ; Neuroblastoma - pathology ; Neurodegeneration ; Neurosciences ; Olea - chemistry ; Polyphenols ; Risk factors ; RNA ; Tumor Cells, Cultured</subject><ispartof>Oxidative medicine and cellular longevity, 2018-01, Vol.2018 (2018), p.1-10</ispartof><rights>Copyright © 2018 Martina Reutzel et al.</rights><rights>COPYRIGHT 2018 John Wiley & Sons, Inc.</rights><rights>Copyright © 2018 Martina Reutzel et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2018 Martina Reutzel et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-c2c443cc85b7433986d6526e92e36ef1b38cb26f4519960ce297398a1299d5983</citedby><cites>FETCH-LOGICAL-c499t-c2c443cc85b7433986d6526e92e36ef1b38cb26f4519960ce297398a1299d5983</cites><orcidid>0000-0002-8002-9983 ; 0000-0002-5895-6385</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232801/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232801/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30510619$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Latini, Alexandra</contributor><contributor>Alexandra Latini</contributor><creatorcontrib>Eckert, Gunter P.</creatorcontrib><creatorcontrib>Marx, Stefan</creatorcontrib><creatorcontrib>Zotzel, Jens</creatorcontrib><creatorcontrib>Silaidos, Carmina</creatorcontrib><creatorcontrib>Grewal, Rekha</creatorcontrib><creatorcontrib>Reutzel, Martina</creatorcontrib><creatorcontrib>Tretzel, Joachim</creatorcontrib><title>Effects of Long-Term Treatment with a Blend of Highly Purified Olive Secoiridoids on Cognition and Brain ATP Levels in Aged NMRI Mice</title><title>Oxidative medicine and cellular longevity</title><addtitle>Oxid Med Cell Longev</addtitle><description>Aging represents a major risk factor for developing neurodegenerative diseases such as Alzheimer’s disease (AD). As components of the Mediterranean diet, olive polyphenols may play a crucial role in the prevention of AD. Since mitochondrial dysfunction acts as a final pathway in both brain aging and AD, respectively, the effects of a mixture of highly purified olive secoiridoids were tested on cognition and ATP levels in a commonly used mouse model for brain aging. Over 6 months, female NMRI mice (12 months of age) were fed with a blend containing highly purified olive secoiridoids (POS) including oleuropein, hydroxytyrosol and oleurosid standardized for 50 mg oleuropein/kg diet (equivalent to 13.75 mg POS/kg b.w.) or the study diet without POS as control. Mice aged 3 months served as young controls. Behavioral tests showed deficits in cognition in aged mice. Levels of ATP and mRNA levels of NADH-reductase, cytochrome-c-oxidase, and citrate synthase were significantly reduced in the brains of aged mice indicating mitochondrial dysfunction. Moreover, gene expression of Sirt1, CREB, Gap43, and GPx-1 was significantly reduced in the brain tissue of aged mice. POS-fed mice showed improved spatial working memory. Furthermore, POS restored brain ATP levels in aged mice which were significantly increased. Our results show that a diet rich in purified olive polyphenols has positive long-term effects on cognition and energy metabolism in the brain of aged mice.</description><subject>Adenosine Triphosphate - metabolism</subject><subject>Advertising executives</subject><subject>Aging</subject><subject>Aging - drug effects</subject><subject>Aging - metabolism</subject><subject>Alzheimer's disease</subject><subject>Analysis</subject><subject>Animal cognition</subject><subject>Animals</subject><subject>Biosynthesis</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain research</subject><subject>Cognition</subject><subject>Cognition - drug effects</subject><subject>Diet</subject><subject>Disease</subject><subject>Disease Models, Animal</subject><subject>Fatty acids</subject><subject>Female</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Iridoids - pharmacology</subject><subject>Laboratory animals</subject><subject>Magnetic resonance imaging</subject><subject>Mice</subject><subject>Nervous system diseases</subject><subject>Neuroblastoma - drug therapy</subject><subject>Neuroblastoma - metabolism</subject><subject>Neuroblastoma - pathology</subject><subject>Neurodegeneration</subject><subject>Neurosciences</subject><subject>Olea - chemistry</subject><subject>Polyphenols</subject><subject>Risk factors</subject><subject>RNA</subject><subject>Tumor Cells, Cultured</subject><issn>1942-0900</issn><issn>1942-0994</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkk9v1DAQxSMEoqVw44wscUGCUP-LE18qbVeFVtrSCpaz5XUmWVeJXexkq36Afu862mULnDh5LP_mzTz5Zdlbgj8TUhTHFJPqmOMSS1Y8yw6J5DTHUvLn-xrjg-xVjDcYC0Y5eZkdMFwQLIg8zB7OmgbMEJFv0MK7Nl9C6NEygB56cAO6s8MaaXTagasn5ty26-4eXY_BNhZqdNXZDaAfYLwNtva2TkoOzX3r7GBTpVPbadDWodnyGi1gA11E061Nzd8uv1-gS2vgdfai0V2EN7vzKPv55Ww5P88XV18v5rNFbriUQ26o4ZwZUxWrkjMmK1GLggqQFJiAhqxYZVZUNLwgUgpsgMoyUZpQKetCVuwoO9nq3o6rHmqTHAbdqdtgex3ulddW_f3i7Fq1fqMEZbTCJAl82AkE_2uEOKjeRgNdpx34MSpKuKw4rkSZ0Pf_oDd-DC7ZSxSjGCcD_IlqdQfKusanuWYSVTOBaUlKWkx7f9pSJvgYAzT7lQlWUwrUlAK1S0HC3_1pcw___vYEfNwCa-tqfWf_Uw4SA41-oikhrGTsEQoDwJE</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Eckert, Gunter P.</creator><creator>Marx, Stefan</creator><creator>Zotzel, Jens</creator><creator>Silaidos, Carmina</creator><creator>Grewal, Rekha</creator><creator>Reutzel, Martina</creator><creator>Tretzel, Joachim</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8002-9983</orcidid><orcidid>https://orcid.org/0000-0002-5895-6385</orcidid></search><sort><creationdate>20180101</creationdate><title>Effects of Long-Term Treatment with a Blend of Highly Purified Olive Secoiridoids on Cognition and Brain ATP Levels in Aged NMRI Mice</title><author>Eckert, Gunter P. ; Marx, Stefan ; Zotzel, Jens ; Silaidos, Carmina ; Grewal, Rekha ; Reutzel, Martina ; Tretzel, Joachim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-c2c443cc85b7433986d6526e92e36ef1b38cb26f4519960ce297398a1299d5983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenosine Triphosphate - metabolism</topic><topic>Advertising executives</topic><topic>Aging</topic><topic>Aging - drug effects</topic><topic>Aging - metabolism</topic><topic>Alzheimer's disease</topic><topic>Analysis</topic><topic>Animal cognition</topic><topic>Animals</topic><topic>Biosynthesis</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain research</topic><topic>Cognition</topic><topic>Cognition - drug effects</topic><topic>Diet</topic><topic>Disease</topic><topic>Disease Models, Animal</topic><topic>Fatty acids</topic><topic>Female</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Iridoids - pharmacology</topic><topic>Laboratory animals</topic><topic>Magnetic resonance imaging</topic><topic>Mice</topic><topic>Nervous system diseases</topic><topic>Neuroblastoma - drug therapy</topic><topic>Neuroblastoma - metabolism</topic><topic>Neuroblastoma - pathology</topic><topic>Neurodegeneration</topic><topic>Neurosciences</topic><topic>Olea - chemistry</topic><topic>Polyphenols</topic><topic>Risk factors</topic><topic>RNA</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eckert, Gunter P.</creatorcontrib><creatorcontrib>Marx, Stefan</creatorcontrib><creatorcontrib>Zotzel, Jens</creatorcontrib><creatorcontrib>Silaidos, Carmina</creatorcontrib><creatorcontrib>Grewal, Rekha</creatorcontrib><creatorcontrib>Reutzel, Martina</creatorcontrib><creatorcontrib>Tretzel, Joachim</creatorcontrib><collection>الدوريات العلمية والإحصائية - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oxidative medicine and cellular longevity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eckert, Gunter P.</au><au>Marx, Stefan</au><au>Zotzel, Jens</au><au>Silaidos, Carmina</au><au>Grewal, Rekha</au><au>Reutzel, Martina</au><au>Tretzel, Joachim</au><au>Latini, Alexandra</au><au>Alexandra Latini</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Long-Term Treatment with a Blend of Highly Purified Olive Secoiridoids on Cognition and Brain ATP Levels in Aged NMRI Mice</atitle><jtitle>Oxidative medicine and cellular longevity</jtitle><addtitle>Oxid Med Cell Longev</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>2018</volume><issue>2018</issue><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>1942-0900</issn><eissn>1942-0994</eissn><abstract>Aging represents a major risk factor for developing neurodegenerative diseases such as Alzheimer’s disease (AD). As components of the Mediterranean diet, olive polyphenols may play a crucial role in the prevention of AD. Since mitochondrial dysfunction acts as a final pathway in both brain aging and AD, respectively, the effects of a mixture of highly purified olive secoiridoids were tested on cognition and ATP levels in a commonly used mouse model for brain aging. Over 6 months, female NMRI mice (12 months of age) were fed with a blend containing highly purified olive secoiridoids (POS) including oleuropein, hydroxytyrosol and oleurosid standardized for 50 mg oleuropein/kg diet (equivalent to 13.75 mg POS/kg b.w.) or the study diet without POS as control. Mice aged 3 months served as young controls. Behavioral tests showed deficits in cognition in aged mice. Levels of ATP and mRNA levels of NADH-reductase, cytochrome-c-oxidase, and citrate synthase were significantly reduced in the brains of aged mice indicating mitochondrial dysfunction. Moreover, gene expression of Sirt1, CREB, Gap43, and GPx-1 was significantly reduced in the brain tissue of aged mice. POS-fed mice showed improved spatial working memory. Furthermore, POS restored brain ATP levels in aged mice which were significantly increased. Our results show that a diet rich in purified olive polyphenols has positive long-term effects on cognition and energy metabolism in the brain of aged mice.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>30510619</pmid><doi>10.1155/2018/4070935</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-8002-9983</orcidid><orcidid>https://orcid.org/0000-0002-5895-6385</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate - metabolism Advertising executives Aging Aging - drug effects Aging - metabolism Alzheimer's disease Analysis Animal cognition Animals Biosynthesis Brain - drug effects Brain - metabolism Brain research Cognition Cognition - drug effects Diet Disease Disease Models, Animal Fatty acids Female Gene expression Humans Iridoids - pharmacology Laboratory animals Magnetic resonance imaging Mice Nervous system diseases Neuroblastoma - drug therapy Neuroblastoma - metabolism Neuroblastoma - pathology Neurodegeneration Neurosciences Olea - chemistry Polyphenols Risk factors RNA Tumor Cells, Cultured |
title | Effects of Long-Term Treatment with a Blend of Highly Purified Olive Secoiridoids on Cognition and Brain ATP Levels in Aged NMRI Mice |
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