2024 Volume 4 Issue 3 Pages reg07-reg13
The formation of selenium (Se) adducts of protein in the liver of rats administered Se in excess of nutritional requirements was confirmed using high-performance liquid chromatography-inductively coupled plasma mass spectrometry (HPLC-ICPMS). Male Wistar rats aged 4 weeks old were divided into three groups and fed a basal Se-deficient diet or basal diet supplemented with 0.2 or 2.0 µg Se/g of selenite for 4 weeks, respectively. The liver Se concentration and GPX activity were markedly elevated in rats fed the Se-added diet; the 2.0 µg Se/g group showed a higher Se concentration than the 0.2 µg Se/g group, but GPX did not differ between the two groups. HPLC-ICPMS analysis of liver protease hydrolysates led to the detection of only selenocystine in the 0.2 µg Se/g group, while the 2.0 µg Se/g group showed the presence of four unknown Se compounds in addition of selenocystine. In another experiment, rats weighing 250 g and previously fed the Se-deficient diet for 4 weeks were intraperitoneally administered 50 µg Se/day of selenite or L-selenomethionine for 7 days, and their liver protease hydrolysates were analyzed by HPLC-ICPMS. In selenite-treated rats, peaks of several unknown Se compounds other than selenocystine were detected. In selenomethionine-treated rats, selenomethionine was detected in addition to selenocystine. Unknown Se compounds were also present, but the number and height of peaks were smaller than in selenite-treated rats. These results indicate that with supranutritional Se, accumulation in organs occurs in the form of Se adducts on selenite exposure and mainly nonspecific insertion of selenomethionine into positions of methionine residues of proteins on selenomethionine exposure.
