Pregled bibliografske jedinice broj: 259886
Bioavailability of selenosugars in rat
Bioavailability of selenosugars in rat // Book of Abstracts, 6th International Symposium on Speciation of Elements in Biological, Environmental and Toxicological Sciences
Bialowieza, 2006. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 259886 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Bioavailability of selenosugars in rat
Autori
Jureša, Dijana ; Blanuša, Maja ; Francesconi, Kevin A. ; Kienzl, Norbert ; Kuehnelt, Doris
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts, 6th International Symposium on Speciation of Elements in Biological, Environmental and Toxicological Sciences
/ - Bialowieza, 2006
Skup
6th International Symposium on Speciation of Elements in Biological, Environmental and Toxicological Sciences
Mjesto i datum
Białowieża, Poljska, 21.06.2006. - 25.06.2006
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Methyl-2-acetamido-2-deoxy-1-seleno-β -D-galactopyranoside; trimethylselenonium iodide; methyl-2-acetamido-2-deoxy-1-seleno-β -D-glucopyranoside; urine; rat
Sažetak
Methyl-2-acetamido-2-deoxy-1-seleno-β -D-galactopyranoside (selenosugar 1) was recently identified as the major urinary selenium metabolite. To obtain information on biological availability and metabolism of selenosugar 1 in relation to biologically available selenite male Wistar strain rats at 8 weeks of age were exposed during 48h to sodium selenite, trimethylselenonium iodide (TMSe), selenosugar 1 or methyl-2-acetamido-2-deoxy-1-seleno-β -D-glucopyranoside (selenosugar 2) in drinking water. Selenium speciation analysis by HPLC/ICPMS was performed on urine samples collected during the exposure. Total selenium in liver, kidney, small intestine and blood was analysed at the end of the experiment by ICPMS following microwave-assisted acid digestion. The major species found in background urine of rats not supplemented with selenium were selenosugar 1 (major metabolite) and TMSe (minor metabolite). The majority of selenium excreted in the urine after ingestion of selenosugars was excreted unchanged, while one part was metabolised, resulting in selenosugar 1 and TMSe as urinary metabolites. As previously reported, ingested TMSe was excreted rapidly and unchanged. Selenium after ingestion of selenite was excreted as selenosugar 1 and TMSe and excretion was slower when compared to selenosugars or TMSe. Ingestion of selenite resulted in increased selenium in the blood and organs, whereas no significant increases in selenium concentration were observed after ingestion of selenosugars or TMSe. The work indicates that selenosugar 1 and selenosugar 2 are at least partly biologically available to rats and undergo metabolism resulting with selenosugar 1 and TMSe as the end products excreted in the urine.
Izvorni jezik
Engleski
Znanstvena područja
Javno zdravstvo i zdravstvena zaštita
POVEZANOST RADA
Projekti:
0022012
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb