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Metabolic pathway for selenium in the body: speciation by HPLC-ICP MS with enriched Se.
Food Addit Contam. 2002 Oct; 19(10):974-83.FA

Abstract

Selenium (Se) is an ultramicro essential nutrient and both inorganic (selenite and selenate) and organic (selenocysteine and selenomethionine) forms of Se can be used as nutritional sources. Metabolic pathways for Se in the body were studied for selenite and selenate, with the use of enriched 82Se, by speciation with separation by gel filtration HPLC and detection by element-specific mass spectrometry with ionization with inductively coupled argon plasma (HPLC-ICP MS). The concentrations of 82Se in organs and body fluids and the distributions of their constituents depending on the dose and time after the intravenous administration of 82Se-selenite and -selenate to rats were determined. Selenite was taken up by red blood cells within several minutes, reduced to selenide by glutathione, and then transported to the plasma, bound selectively to albumin and transferred to the liver. Contrary to selenite, intact selenate was either taken up directly by the liver or excreted into the urine. The 82Se of selenite origin and that of selenate origin were detected in the forms of the two Se peak materials in the liver, A and B. The former one was methylated to the latter in vivo and in vitro. The latter one was identical with the major urinary metabolite and it was identified as Se-methyl-N-acetyl-selenohexosamine (selenosugar). The chemical species-specific metabolic pathway for Se was explained by the metabolic regulation through selenide as the assumed common intermediate for the inorganic and organic Se sources and as the checkpoint metabolite between utilization for the selenoprotein synthesis and methylation for the excretion of Se.

Authors+Show Affiliations

Graduate School of Pharmaceutical Sciences, Chiba University, Chiba 263-8522, Japan. ktsuzuki@p.chiba-u.ac.jpNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Review

Language

eng

PubMed ID

12443560

Citation

Suzuki, K T., and Y Ogra. "Metabolic Pathway for Selenium in the Body: Speciation By HPLC-ICP MS With Enriched Se." Food Additives and Contaminants, vol. 19, no. 10, 2002, pp. 974-83.
Suzuki KT, Ogra Y. Metabolic pathway for selenium in the body: speciation by HPLC-ICP MS with enriched Se. Food Addit Contam. 2002;19(10):974-83.
Suzuki, K. T., & Ogra, Y. (2002). Metabolic pathway for selenium in the body: speciation by HPLC-ICP MS with enriched Se. Food Additives and Contaminants, 19(10), 974-83.
Suzuki KT, Ogra Y. Metabolic Pathway for Selenium in the Body: Speciation By HPLC-ICP MS With Enriched Se. Food Addit Contam. 2002;19(10):974-83. PubMed PMID: 12443560.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Metabolic pathway for selenium in the body: speciation by HPLC-ICP MS with enriched Se. AU - Suzuki,K T, AU - Ogra,Y, PY - 2002/11/22/pubmed PY - 2003/1/7/medline PY - 2002/11/22/entrez SP - 974 EP - 83 JF - Food additives and contaminants JO - Food Addit Contam VL - 19 IS - 10 N2 - Selenium (Se) is an ultramicro essential nutrient and both inorganic (selenite and selenate) and organic (selenocysteine and selenomethionine) forms of Se can be used as nutritional sources. Metabolic pathways for Se in the body were studied for selenite and selenate, with the use of enriched 82Se, by speciation with separation by gel filtration HPLC and detection by element-specific mass spectrometry with ionization with inductively coupled argon plasma (HPLC-ICP MS). The concentrations of 82Se in organs and body fluids and the distributions of their constituents depending on the dose and time after the intravenous administration of 82Se-selenite and -selenate to rats were determined. Selenite was taken up by red blood cells within several minutes, reduced to selenide by glutathione, and then transported to the plasma, bound selectively to albumin and transferred to the liver. Contrary to selenite, intact selenate was either taken up directly by the liver or excreted into the urine. The 82Se of selenite origin and that of selenate origin were detected in the forms of the two Se peak materials in the liver, A and B. The former one was methylated to the latter in vivo and in vitro. The latter one was identical with the major urinary metabolite and it was identified as Se-methyl-N-acetyl-selenohexosamine (selenosugar). The chemical species-specific metabolic pathway for Se was explained by the metabolic regulation through selenide as the assumed common intermediate for the inorganic and organic Se sources and as the checkpoint metabolite between utilization for the selenoprotein synthesis and methylation for the excretion of Se. SN - 0265-203X UR - https://www.unboundmedicine.com/medline/citation/12443560/Metabolic_pathway_for_selenium_in_the_body:_speciation_by_HPLC_ICP_MS_with_enriched_Se_ DB - PRIME DP - Unbound Medicine ER -