Literature DB >> 10781391

Effects of organic and inorganic selenium supplementation on selenoenzyme activity in blood lymphocytes, granulocytes, platelets and erythrocytes.

K M Brown1, K Pickard, F Nicol, G J Beckett, G G Duthie, J R Arthur.   

Abstract

The blood selenium (Se) concentration in the U.K. population has declined by approx. 50% between 1974 and 1991, reflecting a large decrease in dietary Se supply, with intakes only half the reference nutrient intake of 1 microg/kg body weight. Tissue levels of Se are readily influenced by dietary intake. Therefore selenoprotein activity may be sub-optimal due to low Se status, and thus compromise normal cell function. To examine the effects of changing Se intake on selenoproteins, we have determined the relative effectiveness of organic selenomethionine and inorganic sodium selenite (50 microg of Se daily for 28 days) in modulating glutathione peroxidase activities in blood cells from 45 healthy men and women, from a U.K. population. Transient and acute changes in lymphocyte, granulocyte and platelet phospholipid-hydroperoxide glutathione peroxidase (GPx4) activity occurred by day 7 or 14 of sodium selenite treatment and by day 7 in lymphocytes from selenomethionine-treated subjects compared with controls taking a placebo. In contrast, GPx4 activity in granulocytes and platelets in the selenomethionine group increased gradually over the 28 days. Cytosolic glutathione peroxidase (GPx1) activity in these blood cells from both treatment groups increased gradually over the 28 days. For each cellular selenoenzyme activity a significant inter-individual difference (P<0.001) in the extent of the response to Se supplementation was observed, but this was not related to blood Se concentrations either before or after treatments. Significant inverse correlations were evident between baseline enzyme activities and percentage change in activity after 28 days of supplementation [e.g. lymphocyte GPx4, r=-0.695 (P<0.001)], indicating that pre-treatment activity may be sub-optimal as a result of poor Se status. The different and contrasting effects that Se supplementation had on blood selenoenzyme activities may be indicative of a difference in metabolic need for Se regulated at the level of Se-dependent cell function.

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Year:  2000        PMID: 10781391

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  22 in total

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Review 3.  Selenium and selenoproteins in prostanoid metabolism and immunity.

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4.  Genetic variation in GPX1 is associated with GPX1 activity in a comprehensive analysis of genetic variations in selenoenzyme genes and their activity and oxidative stress in humans.

Authors:  Yumie Takata; Irena B King; Johanna W Lampe; Raymond F Burk; Kristina E Hill; Regina M Santella; Alan R Kristal; David J Duggan; Thomas L Vaughan; Ulrike Peters
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Authors:  Edith Lubos; Christoph R Sinning; Renate B Schnabel; Philipp S Wild; Tanja Zeller; Hans J Rupprecht; Christoph Bickel; Karl J Lackner; Dirk Peetz; Joseph Loscalzo; Thomas Münzel; Stefan Blankenberg
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Review 6.  Selenium and the prevention of prostate and colorectal cancer.

Authors:  Ulrike Peters; Yumie Takata
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7.  The impact of cardiopulmonary bypass on selenium status, thyroid function, and oxidative defense in children.

Authors:  R Holzer; B Bockenkamp; P Booker; P Newland; G Ciotti; M Pozzi
Journal:  Pediatr Cardiol       Date:  2004-05-12       Impact factor: 1.655

8.  Antibacterial action of selenium-enriched probiotics against pathogenic Escherichia coli.

Authors:  Jiajun Yang; Kehe Huang; Shunyi Qin; Xianshi Wu; Zhiping Zhao; Fu Chen
Journal:  Dig Dis Sci       Date:  2008-07-10       Impact factor: 3.199

Review 9.  Glutathione metabolism and Parkinson's disease.

Authors:  Michelle Smeyne; Richard Jay Smeyne
Journal:  Free Radic Biol Med       Date:  2013-05-08       Impact factor: 7.376

10.  A 2018 European Thyroid Association Survey on the Use of Selenium Supplementation in Hashimoto's Thyroiditis.

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Journal:  Eur Thyroid J       Date:  2020-01-14
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