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...

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Main Authors: Kazuyo Kaneko, Chikako Kiyose, Tadahiko Ueda, Hisatsugu Ichikawa, Osamu Igarashi
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
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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
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AT chikakokiyose studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol
AT tadahikoueda studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol
AT hisatsuguichikawa studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol
AT osamuigarashi studiesofthemetabolismofatocopherolstereoisomersinratsusing5methyl14csrrandrrratocopherol
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