Selenium metabolism in hepatocytes incubated with selenite, selenate, selenomethionie, Se-methylselenocysteine and  methylseleninc acid and analysed by LC-ICP-MS

TY - JOUR

T1 - Selenium metabolism in hepatocytes incubated with selenite, selenate, selenomethionie, Se-methylselenocysteine and  methylseleninc acid and analysed by LC-ICP-MS

AU - Gabel-Jensen, Charlotte

AU - Gammelgaard, Bente

PY - 2010

Y1 - 2010

N2 - The aim of the present work was to estimate the amounts of selenium metabolites produced in a liver cell model. Five different selenium compounds comprising the inorganic selenium species selenate and selenite, methylseleninic acid (MeSeA) and the selenoamino acids, selenomethionine (SeMet) and Se-methylselenocysteine (Se-MeSeCys) were incubated in rat hepatocytes in amounts of 5 μM for 4 h. The distribution of selenium between media, lysate and insoluble fractions was determined by means of flow injection ICP-MS. Speciation analysis of growth media and lysate samples by LC-ICP-MS showed only limited metabolism of selenate, SeMet, and Se-MeSeCys, while MeSeA and selenite were extensively metabolized. Small molecule metabolites constituted less than 5% of the applied amount and some of the transformed selenium was detected in the protein fraction of the samples although all Se could not be accounted for. This result indicates that more important metabolism pathways may be related to protein bound selenium.

AB - The aim of the present work was to estimate the amounts of selenium metabolites produced in a liver cell model. Five different selenium compounds comprising the inorganic selenium species selenate and selenite, methylseleninic acid (MeSeA) and the selenoamino acids, selenomethionine (SeMet) and Se-methylselenocysteine (Se-MeSeCys) were incubated in rat hepatocytes in amounts of 5 μM for 4 h. The distribution of selenium between media, lysate and insoluble fractions was determined by means of flow injection ICP-MS. Speciation analysis of growth media and lysate samples by LC-ICP-MS showed only limited metabolism of selenate, SeMet, and Se-MeSeCys, while MeSeA and selenite were extensively metabolized. Small molecule metabolites constituted less than 5% of the applied amount and some of the transformed selenium was detected in the protein fraction of the samples although all Se could not be accounted for. This result indicates that more important metabolism pathways may be related to protein bound selenium.

KW - Former Faculty of Pharmaceutical Sciences

U2 - 10.1039/b921365a

DO - 10.1039/b921365a

M3 - Journal article

SN - 0267-9477

VL - 25

SP - 414

EP - 118

JO - Journal of Analytical Atomic Spectrometry

JF - Journal of Analytical Atomic Spectrometry

ER -