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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Veröffentlicht in:Nutrients 2014-07, Vol.6 (8), p.3000-3017
Hauptverfasser: Marín, Tamara, Contreras, Pablo, Castro, Juan Francisco, Chamorro, David, Balboa, Elisa, Bosch-Morató, Mònica, Muñoz, Francisco J, Alvarez, Alejandra R, Zanlungo, Silvana
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container_end_page 3017
container_issue 8
container_start_page 3000
container_title Nutrients
container_volume 6
creator Marín, Tamara
Contreras, Pablo
Castro, Juan Francisco
Chamorro, David
Balboa, Elisa
Bosch-Morató, Mònica
Muñoz, Francisco J
Alvarez, Alejandra R
Zanlungo, Silvana
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.
doi_str_mv 10.3390/nu6083000
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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 &amp; derivatives ; Tyrosine - metabolism ; Vitamin E ; Vitamin E - administration &amp; 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. 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source MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Recercat; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access
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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