Source:http://linkedlifedata.com/resource/pubmed/id/20183830
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2010-5-17
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pubmed:abstractText |
In Western societies the apolipoprotein E4 (apoE4) genotype is associated with increased morbidity and mortality and represents a significant risk factor for cardiovascular and Alzheimer's disease. In a recent study we observed significantly lower tissue alpha-tocopherol (alpha-TOH) concentrations in apoE4 compared with apoE3 mice. Furthermore, genes encoding for proteins involved in peripheral alpha-TOH transport and degradation were affected by the apoE genotype. Thus, the apoE4 genotype may be associated with lower vitamin E retention in peripheral tissues. This is possibly related to an altered lipoprotein metabolism including increased alpha-TOH retention in LDL, a decreased expression of lipoprotein receptors and impaired cellular vitamin E delivery system, and a greater intracellular degradation of tocopherols in the apoE4 genotype. An increasing number of studies in cultured cells, transgenic mice and human volunteers indicate a more pro-inflammatory state associated with the apoE4 allele. In apoE4 macrophages there is an enhanced transactivation of the key redox sensitive transcription factor NF-kappaB accompanied by a higher production of pro-inflammatory molecules (tumor necrosis factor alpha, interleukin 1beta, macrophage inflammatory protein 1-alpha) and a lower production of anti-inflammatory interleukin 10, as compared with apoE3 macrophages. Both tissue vitamin E retention and biomarkers of chronic inflammation may be affected by the apoE genotype.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Apolipoprotein E3,
http://linkedlifedata.com/resource/pubmed/chemical/Apolipoprotein E4,
http://linkedlifedata.com/resource/pubmed/chemical/Apolipoproteins E,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Vitamin E,
http://linkedlifedata.com/resource/pubmed/chemical/alpha-Tocopherol
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1613-4133
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
54
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
623-30
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pubmed:meshHeading |
pubmed-meshheading:20183830-Alzheimer Disease,
pubmed-meshheading:20183830-Animals,
pubmed-meshheading:20183830-Apolipoprotein E3,
pubmed-meshheading:20183830-Apolipoprotein E4,
pubmed-meshheading:20183830-Apolipoproteins E,
pubmed-meshheading:20183830-Cardiovascular Diseases,
pubmed-meshheading:20183830-Genotype,
pubmed-meshheading:20183830-Germany,
pubmed-meshheading:20183830-Humans,
pubmed-meshheading:20183830-Inflammation,
pubmed-meshheading:20183830-Mice,
pubmed-meshheading:20183830-Polymorphism, Genetic,
pubmed-meshheading:20183830-RNA, Messenger,
pubmed-meshheading:20183830-Vitamin E,
pubmed-meshheading:20183830-alpha-Tocopherol
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pubmed:year |
2010
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pubmed:articleTitle |
Implications of apolipoprotein E genotype on inflammation and vitamin E status.
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pubmed:affiliation |
Institute of Human Nutrition and Food Science, Christian-Albrechts-University, Kiel, Germany.
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pubmed:publicationType |
Journal Article,
Review
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