Characterization of new conjugated metabolites in bile of rats administered 24,25-dihydroxyvitamin D3 and 25-hydroxyvitamin D3

被引:20
作者
Higashi, T
Miura, K
Kikuchi, R
Shimada, K
Hiyamizu, H
Ooi, H
Iwabuchi, Y
Hatakeyama, S
Kubodera, N
机构
[1] Kanazawa Univ, Fac Pharmaceut Sci, Kanazawa, Ishikawa 9200934, Japan
[2] Nagasaki Univ, Fac Pharmaceut Sci, Nagasaki 8528521, Japan
[3] Chugai Pharmaceut Co Ltd, Chuo Ku, Tokyo 1048301, Japan
关键词
24,25-dihydroxyvitamin D-3; 25-hydroxyvitamin D-3; rat bile; conjugated metabolite; liquid chromatography tandem mass spectrometry; 3-epi-24,25-dihydroxyvitamin D-3; 24-glucuronide;
D O I
10.1016/S0039-128X(00)00087-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The characterization of new conjugated vitamin D metabolites in rat bile was performed using HPLC, liquid chromatography/tandem mass spectrometry combined derivatization, and GC-MS. After the administration of 24,25-dihydroxyvitamin D-3 to rats, 23,25-dihydroxy-24-oxovitamin D-3 23-glucuronide, 3-epi-24,25-dihydroxyvitamin D-3 24-glucuronide, and 24,25-dihydroxyvitamin D-3 3-sulfate were obtained as new biliary metabolites together with 24,25-dihydroxyvitamin D-3 3- and 24-glucuronides. The above metabolites, except 24,25-dihydroxyvitamin D-3 3-glucuronide, were obtained from rats dosed with 25-hydroxyvitamin D-3. 23,25-Dihydroxyvitamin D-3 23-glucuronide was also obtained from the bile of rats administered 25-hydroxyvitamin D-3 in addition to its 3-glucuronide, 25-glucuronide, and 3-sulfate. Thus, it was found that 24,25-dihydroxyvitamin D-3 and 25-hydroxyvitamin D-3 were directly conjugated as glucuronide and sulfate, whereas at the C-23 position, they were hydroxylated and then conjugated. Furthermore, we found that the C-3 epimerization acts as one of the important pathways in vitamin D metabolism. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:281 / 294
页数:14
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