Literature DB >> 1858872

Response of rat selenoprotein P to selenium administration and fate of its selenium.

R F Burk1, K E Hill, R Read, T Bellew.   

Abstract

Selenoprotein P is a glycoprotein that contains greater than 60% of the selenium in rat plasma. Physiological experiments were undertaken to gain insight into selenoprotein P function. Selenium-deficient rats were injected with doses of selenium ranging from 25 to 200 micrograms/kg, and the appearance of selenoprotein P was compared with the appearance of glutathione peroxidase activity in plasma and in liver. Selenoprotein P concentration increased to 35% of control by 6 h, whereas glutathione peroxidase activity increased minimally or not at all. Moreover, in rats given 100 and 200 micrograms selenium/kg, selenoprotein P reached 75% of its concentration in control rats at 24 h, whereas glutathione peroxidase activity reached only 6% of control. Cycloheximide pretreatment blocked the appearance of selenoprotein P in response to selenium injection. Male and female rats had similar concentrations of selenoprotein P. Partially purified selenoprotein P and plasma glutathione peroxidase labeled with 75Se were administered intravenously to selenium-deficient and control rats. 75Se given as selenoprotein P disappeared more rapidly from plasma than did 75Se given as glutathione peroxidase. Selenium deficiency did not significantly affect 75Se disappearance from plasma. At 2 h, brain, but not other tissues, took up more 75Se in selenium-deficient rats than in control rats when 75Se was given as selenoprotein P. This suggests that brain has a specific uptake mechanism for selenium given in the form of selenoprotein P. These results demonstrate that several physiological properties distinguish selenoprotein P from glutathione peroxidase. However, they do not clearly indicate its function.

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Year:  1991        PMID: 1858872     DOI: 10.1152/ajpendo.1991.261.1.E26

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  18 in total

1.  A human model of selenium that integrates metabolism from selenite and selenomethionine.

Authors:  Meryl E Wastney; Gerald F Combs; Wesley K Canfield; Philip R Taylor; Kristine Y Patterson; A David Hill; James E Moler; Blossom H Patterson
Journal:  J Nutr       Date:  2011-02-02       Impact factor: 4.798

Review 2.  Selenium metabolism and bioavailability.

Authors:  L A Daniels
Journal:  Biol Trace Elem Res       Date:  1996-09       Impact factor: 3.738

Review 3.  Selenoproteins: molecular pathways and physiological roles.

Authors:  Vyacheslav M Labunskyy; Dolph L Hatfield; Vadim N Gladyshev
Journal:  Physiol Rev       Date:  2014-07       Impact factor: 37.312

Review 4.  More roles for selenoprotein P: local selenium storage and recycling protein in the brain.

Authors:  Des R Richardson
Journal:  Biochem J       Date:  2005-03-01       Impact factor: 3.857

5.  Deletion of selenoprotein P upregulates urinary selenium excretion and depresses whole-body selenium content.

Authors:  Raymond F Burk; Kristina E Hill; Amy K Motley; Lori M Austin; Brooke K Norsworthy
Journal:  Biochim Biophys Acta       Date:  2006-08-18

6.  Uptake and Utilization of Selenium from Selenoprotein P.

Authors:  Sumangala Shetty; John R Marsicano; Paul R Copeland
Journal:  Biol Trace Elem Res       Date:  2017-05-09       Impact factor: 3.738

7.  Loss of selenium from selenoproteins: conversion of selenocysteine to dehydroalanine in vitro.

Authors:  Shuguang Ma; Richard M Caprioli; Kristina E Hill; Raymond F Burk
Journal:  J Am Soc Mass Spectrom       Date:  2003-06       Impact factor: 3.109

Review 8.  Some properties of selenoprotein P.

Authors:  R F Burk; K E Hill
Journal:  Biol Trace Elem Res       Date:  1992 Apr-Jun       Impact factor: 3.738

9.  Purification from bovine serum of a survival-promoting factor for cultured central neurons and its identification as selenoprotein-P.

Authors:  J Yan; J N Barrett
Journal:  J Neurosci       Date:  1998-11-01       Impact factor: 6.167

10.  Deletion of apolipoprotein E receptor-2 in mice lowers brain selenium and causes severe neurological dysfunction and death when a low-selenium diet is fed.

Authors:  Raymond F Burk; Kristina E Hill; Gary E Olson; Edwin J Weeber; Amy K Motley; Virginia P Winfrey; Lori M Austin
Journal:  J Neurosci       Date:  2007-06-06       Impact factor: 6.167

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