Vitamin E dietary supplementation improves neurological symptoms and decreases c-Abl/p73 activation in Niemann-Pick C mice
Niemann-Pick C (NPC) disease is a fatal neurodegenerative disorder characterized by the accumulation of free cholesterol in lysosomes. We have previously reported that oxidative stress is the main upstream stimulus activating the proapoptotic c-Abl/p73 pathway in NPC neurons. We have also observed a...
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description | Niemann-Pick C (NPC) disease is a fatal neurodegenerative disorder characterized by the accumulation of free cholesterol in lysosomes. We have previously reported that oxidative stress is the main upstream stimulus activating the proapoptotic c-Abl/p73 pathway in NPC neurons. We have also observed accumulation of vitamin E in NPC lysosomes, which could lead to a potential decrease of its bioavailability. Our aim was to determine if dietary vitamin E supplementation could improve NPC disease in mice. NPC mice received an alpha-tocopherol (α-TOH) supplemented diet and neurological symptoms, survival, Purkinje cell loss, α-TOH and nitrotyrosine levels, astrogliosis, and the c-Abl/p73 pathway functions were evaluated. In addition, the effect of α-TOH on the c-Abl/p73 pathway was evaluated in an in vitro NPC neuron model. The α-TOH rich diet delayed loss of weight, improved coordination and locomotor function and increased the survival of NPC mice. We found increased Purkinje neurons and α-TOH levels and reduced astrogliosis, nitrotyrosine and phosphorylated p73 in cerebellum. A decrease of c-Abl/p73 activation was also observed in the in vitro NPC neurons treated with α-TOH. In conclusion, our results show that vitamin E can delay neurodegeneration in NPC mice and suggest that its supplementation in the diet could be useful for the treatment of NPC patients. |
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We have previously reported that oxidative stress is the main upstream stimulus activating the proapoptotic c-Abl/p73 pathway in NPC neurons. We have also observed accumulation of vitamin E in NPC lysosomes, which could lead to a potential decrease of its bioavailability. Our aim was to determine if dietary vitamin E supplementation could improve NPC disease in mice. NPC mice received an alpha-tocopherol (α-TOH) supplemented diet and neurological symptoms, survival, Purkinje cell loss, α-TOH and nitrotyrosine levels, astrogliosis, and the c-Abl/p73 pathway functions were evaluated. In addition, the effect of α-TOH on the c-Abl/p73 pathway was evaluated in an in vitro NPC neuron model. The α-TOH rich diet delayed loss of weight, improved coordination and locomotor function and increased the survival of NPC mice. We found increased Purkinje neurons and α-TOH levels and reduced astrogliosis, nitrotyrosine and phosphorylated p73 in cerebellum. A decrease of c-Abl/p73 activation was also observed in the in vitro NPC neurons treated with α-TOH. In conclusion, our results show that vitamin E can delay neurodegeneration in NPC mice and suggest that its supplementation in the diet could be useful for the treatment of NPC patients.</description><identifier>ISSN: 2072-6643</identifier><identifier>EISSN: 2072-6643</identifier><identifier>DOI: 10.3390/nu6083000</identifier><identifier>PMID: 25079853</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>alpha-Tocopherol ; Animals ; Antioxidants ; Apoptosis ; Ataxia ; bioavailability ; c-Abl ; Caspase 3 - genetics ; Caspase 3 - metabolism ; Cell Line ; Cell Survival - drug effects ; cerebellum ; Cholesterol ; Diet ; Dietary Supplements ; Disease Models, Animal ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; Lysosomes ; Lysosomes - drug effects ; Lysosomes - metabolism ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; Mutation ; Neurodegeneration ; neurodegenerative diseases ; Neurodegenerative Diseases - drug therapy ; Neurons ; Niemann-Pick C ; Niemann-Pick Disease, Type C - drug therapy ; Niemann-Pick Disease, Type C - genetics ; Nuclear Proteins - genetics ; Nuclear Proteins - metabolism ; Oxidative stress ; Oxidative Stress - drug effects ; patients ; Proteïna tirosina-quinasa ; Proteïnes de la sang ; Proto-Oncogene Proteins c-abl - genetics ; Proto-Oncogene Proteins c-abl - metabolism ; Receptors ; Signal Transduction ; Tumor Protein p73 ; Tumor Suppressor Proteins - genetics ; Tumor Suppressor Proteins - metabolism ; Tyrosine - analogs & derivatives ; Tyrosine - metabolism ; Vitamin E ; Vitamin E - administration & dosage ; weight loss</subject><ispartof>Nutrients, 2014-07, Vol.6 (8), p.3000-3017</ispartof><rights>Copyright MDPI AG 2014</rights><rights>This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. https://creativecommons.org/licenses/by/3.0/ info:eu-repo/semantics/openAccess</rights><rights>2014 by the authors; licensee MDPI, Basel, Switzerland. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-ec43e892790743642d3352c84f9a8eab3a623b6f93b793dcfd1a4e0a85a1d5283</citedby><cites>FETCH-LOGICAL-c478t-ec43e892790743642d3352c84f9a8eab3a623b6f93b793dcfd1a4e0a85a1d5283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145291/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145291/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,26951,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25079853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marín, Tamara</creatorcontrib><creatorcontrib>Contreras, Pablo</creatorcontrib><creatorcontrib>Castro, Juan Francisco</creatorcontrib><creatorcontrib>Chamorro, David</creatorcontrib><creatorcontrib>Balboa, Elisa</creatorcontrib><creatorcontrib>Bosch-Morató, Mònica</creatorcontrib><creatorcontrib>Muñoz, Francisco J</creatorcontrib><creatorcontrib>Alvarez, Alejandra R</creatorcontrib><creatorcontrib>Zanlungo, Silvana</creatorcontrib><title>Vitamin E dietary supplementation improves neurological symptoms and decreases c-Abl/p73 activation in Niemann-Pick C mice</title><title>Nutrients</title><addtitle>Nutrients</addtitle><description>Niemann-Pick C (NPC) disease is a fatal neurodegenerative disorder characterized by the accumulation of free cholesterol in lysosomes. We have previously reported that oxidative stress is the main upstream stimulus activating the proapoptotic c-Abl/p73 pathway in NPC neurons. We have also observed accumulation of vitamin E in NPC lysosomes, which could lead to a potential decrease of its bioavailability. Our aim was to determine if dietary vitamin E supplementation could improve NPC disease in mice. NPC mice received an alpha-tocopherol (α-TOH) supplemented diet and neurological symptoms, survival, Purkinje cell loss, α-TOH and nitrotyrosine levels, astrogliosis, and the c-Abl/p73 pathway functions were evaluated. In addition, the effect of α-TOH on the c-Abl/p73 pathway was evaluated in an in vitro NPC neuron model. The α-TOH rich diet delayed loss of weight, improved coordination and locomotor function and increased the survival of NPC mice. We found increased Purkinje neurons and α-TOH levels and reduced astrogliosis, nitrotyrosine and phosphorylated p73 in cerebellum. A decrease of c-Abl/p73 activation was also observed in the in vitro NPC neurons treated with α-TOH. In conclusion, our results show that vitamin E can delay neurodegeneration in NPC mice and suggest that its supplementation in the diet could be useful for the treatment of NPC patients.</description><subject>alpha-Tocopherol</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Ataxia</subject><subject>bioavailability</subject><subject>c-Abl</subject><subject>Caspase 3 - genetics</subject><subject>Caspase 3 - metabolism</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>cerebellum</subject><subject>Cholesterol</subject><subject>Diet</subject><subject>Dietary Supplements</subject><subject>Disease Models, Animal</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Lysosomes</subject><subject>Lysosomes - drug effects</subject><subject>Lysosomes - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Knockout</subject><subject>Mutation</subject><subject>Neurodegeneration</subject><subject>neurodegenerative diseases</subject><subject>Neurodegenerative Diseases - drug therapy</subject><subject>Neurons</subject><subject>Niemann-Pick C</subject><subject>Niemann-Pick Disease, Type C - drug therapy</subject><subject>Niemann-Pick Disease, Type C - genetics</subject><subject>Nuclear Proteins - genetics</subject><subject>Nuclear Proteins - metabolism</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>patients</subject><subject>Proteïna tirosina-quinasa</subject><subject>Proteïnes de la sang</subject><subject>Proto-Oncogene Proteins c-abl - genetics</subject><subject>Proto-Oncogene Proteins c-abl - metabolism</subject><subject>Receptors</subject><subject>Signal Transduction</subject><subject>Tumor Protein p73</subject><subject>Tumor Suppressor Proteins - genetics</subject><subject>Tumor Suppressor Proteins - metabolism</subject><subject>Tyrosine - analogs & derivatives</subject><subject>Tyrosine - metabolism</subject><subject>Vitamin E</subject><subject>Vitamin E - administration & dosage</subject><subject>weight loss</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>XX2</sourceid><recordid>eNqFkk1vFSEUhonR2KZ24R8wJG50MZbPgdmYNDfVNmnUhbolDHOmUgcYYeYm9dfLtdeb6kYSwiE854X3cBB6TskbzjtyFteWaE4IeYSOGVGsaVvBHz-Ij9BpKbdkNxRRLX-KjpgkqtOSH6OfX_1ig4_4Ag8eFpvvcFnneYIAcbGLTxH7MOe0hYIjrDlN6cY7O-FyF-YlhYJtHPAALoMtlXHNeT-dzYpj6xa_3StE_MFDsDE2n7z7jjc4eAfP0JPRTgVO9-sJ-vLu4vPmsrn--P5qc37dOKH00oATHHTHVEeU4K1gA-eSOS3GzmqwPbct4307drxXHR_cOFArgFgtLR0k0_wEvb3Xndc-wOCqsWwnM2cfql2TrDd_n0T_zdykrRFUSNbRKkDvBVxZncngIDu7_E48bHZzV3HDqZRC1JxX-0tz-rFCWUzwxcE02QhpLYYxRTXjUuv_olWQEtoRJiv68h_0Nq051upVqq2C9XtJpV7v35tTKRnGg1dKzK5nzKFnKvviYXEO5J8O4b8AT3G8bA</recordid><startdate>20140730</startdate><enddate>20140730</enddate><creator>Marín, Tamara</creator><creator>Contreras, Pablo</creator><creator>Castro, Juan Francisco</creator><creator>Chamorro, David</creator><creator>Balboa, Elisa</creator><creator>Bosch-Morató, Mònica</creator><creator>Muñoz, Francisco J</creator><creator>Alvarez, Alejandra R</creator><creator>Zanlungo, Silvana</creator><general>MDPI AG</general><general>MDPI</general><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>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>XX2</scope><scope>5PM</scope></search><sort><creationdate>20140730</creationdate><title>Vitamin E dietary supplementation improves neurological symptoms and decreases c-Abl/p73 activation in Niemann-Pick C mice</title><author>Marín, Tamara ; Contreras, Pablo ; Castro, Juan Francisco ; Chamorro, David ; Balboa, Elisa ; Bosch-Morató, Mònica ; Muñoz, Francisco J ; Alvarez, Alejandra R ; Zanlungo, Silvana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-ec43e892790743642d3352c84f9a8eab3a623b6f93b793dcfd1a4e0a85a1d5283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>alpha-Tocopherol</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Ataxia</topic><topic>bioavailability</topic><topic>c-Abl</topic><topic>Caspase 3 - genetics</topic><topic>Caspase 3 - metabolism</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>cerebellum</topic><topic>Cholesterol</topic><topic>Diet</topic><topic>Dietary Supplements</topic><topic>Disease Models, Animal</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Lysosomes</topic><topic>Lysosomes - drug effects</topic><topic>Lysosomes - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Knockout</topic><topic>Mutation</topic><topic>Neurodegeneration</topic><topic>neurodegenerative diseases</topic><topic>Neurodegenerative Diseases - drug therapy</topic><topic>Neurons</topic><topic>Niemann-Pick C</topic><topic>Niemann-Pick Disease, Type C - drug therapy</topic><topic>Niemann-Pick Disease, Type C - genetics</topic><topic>Nuclear Proteins - genetics</topic><topic>Nuclear Proteins - metabolism</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>patients</topic><topic>Proteïna tirosina-quinasa</topic><topic>Proteïnes de la sang</topic><topic>Proto-Oncogene Proteins c-abl - genetics</topic><topic>Proto-Oncogene Proteins c-abl - metabolism</topic><topic>Receptors</topic><topic>Signal Transduction</topic><topic>Tumor Protein p73</topic><topic>Tumor Suppressor Proteins - genetics</topic><topic>Tumor Suppressor Proteins - metabolism</topic><topic>Tyrosine - analogs & derivatives</topic><topic>Tyrosine - metabolism</topic><topic>Vitamin E</topic><topic>Vitamin E - administration & dosage</topic><topic>weight loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marín, Tamara</creatorcontrib><creatorcontrib>Contreras, Pablo</creatorcontrib><creatorcontrib>Castro, Juan Francisco</creatorcontrib><creatorcontrib>Chamorro, David</creatorcontrib><creatorcontrib>Balboa, Elisa</creatorcontrib><creatorcontrib>Bosch-Morató, Mònica</creatorcontrib><creatorcontrib>Muñoz, Francisco J</creatorcontrib><creatorcontrib>Alvarez, Alejandra R</creatorcontrib><creatorcontrib>Zanlungo, Silvana</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>Recercat</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nutrients</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marín, Tamara</au><au>Contreras, Pablo</au><au>Castro, Juan Francisco</au><au>Chamorro, David</au><au>Balboa, Elisa</au><au>Bosch-Morató, Mònica</au><au>Muñoz, Francisco J</au><au>Alvarez, Alejandra R</au><au>Zanlungo, Silvana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vitamin E dietary supplementation improves neurological symptoms and decreases c-Abl/p73 activation in Niemann-Pick C mice</atitle><jtitle>Nutrients</jtitle><addtitle>Nutrients</addtitle><date>2014-07-30</date><risdate>2014</risdate><volume>6</volume><issue>8</issue><spage>3000</spage><epage>3017</epage><pages>3000-3017</pages><issn>2072-6643</issn><eissn>2072-6643</eissn><abstract>Niemann-Pick C (NPC) disease is a fatal neurodegenerative disorder characterized by the accumulation of free cholesterol in lysosomes. We have previously reported that oxidative stress is the main upstream stimulus activating the proapoptotic c-Abl/p73 pathway in NPC neurons. We have also observed accumulation of vitamin E in NPC lysosomes, which could lead to a potential decrease of its bioavailability. Our aim was to determine if dietary vitamin E supplementation could improve NPC disease in mice. NPC mice received an alpha-tocopherol (α-TOH) supplemented diet and neurological symptoms, survival, Purkinje cell loss, α-TOH and nitrotyrosine levels, astrogliosis, and the c-Abl/p73 pathway functions were evaluated. In addition, the effect of α-TOH on the c-Abl/p73 pathway was evaluated in an in vitro NPC neuron model. The α-TOH rich diet delayed loss of weight, improved coordination and locomotor function and increased the survival of NPC mice. We found increased Purkinje neurons and α-TOH levels and reduced astrogliosis, nitrotyrosine and phosphorylated p73 in cerebellum. A decrease of c-Abl/p73 activation was also observed in the in vitro NPC neurons treated with α-TOH. In conclusion, our results show that vitamin E can delay neurodegeneration in NPC mice and suggest that its supplementation in the diet could be useful for the treatment of NPC patients.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>25079853</pmid><doi>10.3390/nu6083000</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alpha-Tocopherol Animals Antioxidants Apoptosis Ataxia bioavailability c-Abl Caspase 3 - genetics Caspase 3 - metabolism Cell Line Cell Survival - drug effects cerebellum Cholesterol Diet Dietary Supplements Disease Models, Animal DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism Lysosomes Lysosomes - drug effects Lysosomes - metabolism Male Mice Mice, Inbred BALB C Mice, Knockout Mutation Neurodegeneration neurodegenerative diseases Neurodegenerative Diseases - drug therapy Neurons Niemann-Pick C Niemann-Pick Disease, Type C - drug therapy Niemann-Pick Disease, Type C - genetics Nuclear Proteins - genetics Nuclear Proteins - metabolism Oxidative stress Oxidative Stress - drug effects patients Proteïna tirosina-quinasa Proteïnes de la sang Proto-Oncogene Proteins c-abl - genetics Proto-Oncogene Proteins c-abl - metabolism Receptors Signal Transduction Tumor Protein p73 Tumor Suppressor Proteins - genetics Tumor Suppressor Proteins - metabolism Tyrosine - analogs & derivatives Tyrosine - metabolism Vitamin E Vitamin E - administration & dosage weight loss |
title | Vitamin E dietary supplementation improves neurological symptoms and decreases c-Abl/p73 activation in Niemann-Pick C mice |
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