Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherol
Abstract: We investigated the distribution and metabolism of SRR-α-tocopherol (SRR-α-Toc), synthetic α-Toc compared with RRR-α-Toc, in rats after a single oral administration of 2 mg (20 μCi) SRR- and RRR-α-[5-methyl-14C]Toc. In the liver, there was no difference in the recovery of radioactivity unt...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2000-03-01
|
Series: | Journal of Lipid Research |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520344746 |
id |
doaj-59444735690c4315bca63fd30f631f69 |
---|---|
record_format |
Article |
spelling |
doaj-59444735690c4315bca63fd30f631f692021-04-27T04:46:58ZengElsevierJournal of Lipid Research0022-22752000-03-01413357367Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherolKazuyo Kaneko0Chikako Kiyose1Tadahiko Ueda2Hisatsugu Ichikawa3Osamu Igarashi4Institute of Environmental Science for Human Life, Ochanomizu University, Bunkyo-ku, Tokyo 112-8610, JapanTo whom correspondence should be addressed; Institute of Environmental Science for Human Life, Ochanomizu University, Bunkyo-ku, Tokyo 112-8610, JapanTokyo Metropolitan Research Institute for Environmental Protection, Koto-ku, Tokyo 136-0075, JapanTokyo Metropolitan Research Laboratory of Public Health, Shinjuku-ku, Tokyo 169-0073, JapanInstitute of Environmental Science for Human Life, Ochanomizu University, Bunkyo-ku, Tokyo 112-8610, JapanAbstract: We investigated the distribution and metabolism of SRR-α-tocopherol (SRR-α-Toc), synthetic α-Toc compared with RRR-α-Toc, in rats after a single oral administration of 2 mg (20 μCi) SRR- and RRR-α-[5-methyl-14C]Toc. In the liver, there was no difference in the recovery of radioactivity until 12 h after administration, and it reached a maximum of 4.4% of the dose after 12 h, but in other tissues, radioactivity derived from RRR-α-Toc was clearly higher than that derived from SRR-α-Toc after 12 h. For 96 h after administration, urinary excretions of SRR-α-Toc were 7.8% of the dose and significantly greater than that of RRR-α-Toc, which was 1.3% of the dose. On the other hand, total fecal excretions of SRR- and RRR-α-Toc were 87.6% and 83.0%, respectively. Therefore, radioactivity in the urine was assumed to have transferred out of the liver. Furthermore, the urine samples were hydrolyzed with 3 N methanolic HCl and analyzed by high performance liquid chromatography (HPLC) and liquid chromatography/mass spectrometry. The results showed that about 73% of the total radioactivity injected into HPLC was found to be 2,5,7,8-tetramethyl-2-(2′-carboxyethyl)-6-hydroxy chroman (α-CEHC), as well as RRR-α-Toc. Thus, there is no difference between SRR-α-Toc and RRR-α-Toc in metabolic pathways, and it is suggested that SRR-α-Toc discriminated in the liver is rapidly metabolized by the liver and excreted as the conjugate of α-CEHC in the urine. —Kaneko, K., C. Kiyose, T. Ueda, H. Ichikawa, and O. Igarishi. Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methy1-14C]SRR- and RRR-α-tocopherol. J. Lipid Res. 2000. 41: 357–367.http://www.sciencedirect.com/science/article/pii/S0022227520344746RRR-α-tocopherolSRR-α-tocopherolRRR-α-[5-methyl-14C]tocopherolSRR-α-[5-methyl-14C]tocopherolα-CEHCα-tocopherol metabolism in vivo |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kazuyo Kaneko Chikako Kiyose Tadahiko Ueda Hisatsugu Ichikawa Osamu Igarashi |
spellingShingle |
Kazuyo Kaneko Chikako Kiyose Tadahiko Ueda Hisatsugu Ichikawa Osamu Igarashi Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherol Journal of Lipid Research RRR-α-tocopherol SRR-α-tocopherol RRR-α-[5-methyl-14C]tocopherol SRR-α-[5-methyl-14C]tocopherol α-CEHC α-tocopherol metabolism in vivo |
author_facet |
Kazuyo Kaneko Chikako Kiyose Tadahiko Ueda Hisatsugu Ichikawa Osamu Igarashi |
author_sort |
Kazuyo Kaneko |
title |
Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherol |
title_short |
Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherol |
title_full |
Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherol |
title_fullStr |
Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherol |
title_full_unstemmed |
Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14C]SRR- and RRR-α-tocopherol |
title_sort |
studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methyl-14c]srr- and rrr-α-tocopherol |
publisher |
Elsevier |
series |
Journal of Lipid Research |
issn |
0022-2275 |
publishDate |
2000-03-01 |
description |
Abstract: We investigated the distribution and metabolism of SRR-α-tocopherol (SRR-α-Toc), synthetic α-Toc compared with RRR-α-Toc, in rats after a single oral administration of 2 mg (20 μCi) SRR- and RRR-α-[5-methyl-14C]Toc. In the liver, there was no difference in the recovery of radioactivity until 12 h after administration, and it reached a maximum of 4.4% of the dose after 12 h, but in other tissues, radioactivity derived from RRR-α-Toc was clearly higher than that derived from SRR-α-Toc after 12 h. For 96 h after administration, urinary excretions of SRR-α-Toc were 7.8% of the dose and significantly greater than that of RRR-α-Toc, which was 1.3% of the dose. On the other hand, total fecal excretions of SRR- and RRR-α-Toc were 87.6% and 83.0%, respectively. Therefore, radioactivity in the urine was assumed to have transferred out of the liver. Furthermore, the urine samples were hydrolyzed with 3 N methanolic HCl and analyzed by high performance liquid chromatography (HPLC) and liquid chromatography/mass spectrometry. The results showed that about 73% of the total radioactivity injected into HPLC was found to be 2,5,7,8-tetramethyl-2-(2′-carboxyethyl)-6-hydroxy chroman (α-CEHC), as well as RRR-α-Toc. Thus, there is no difference between SRR-α-Toc and RRR-α-Toc in metabolic pathways, and it is suggested that SRR-α-Toc discriminated in the liver is rapidly metabolized by the liver and excreted as the conjugate of α-CEHC in the urine. —Kaneko, K., C. Kiyose, T. Ueda, H. Ichikawa, and O. Igarishi. Studies of the metabolism of α-tocopherol stereoisomers in rats using [5-methy1-14C]SRR- and RRR-α-tocopherol. J. Lipid Res. 2000. 41: 357–367. |
topic |
RRR-α-tocopherol SRR-α-tocopherol RRR-α-[5-methyl-14C]tocopherol SRR-α-[5-methyl-14C]tocopherol α-CEHC α-tocopherol metabolism in vivo |
url |
http://www.sciencedirect.com/science/article/pii/S0022227520344746 |
work_keys_str_mv |
AT kazuyokaneko studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol AT chikakokiyose studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol AT tadahikoueda studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol AT hisatsuguichikawa studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol AT osamuigarashi studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol |
_version_ |
1721506336477282304 |