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Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph
BACKGROUND: Dietary sphingolipids have various biofunctions, including skin barrier improvement and anti-inflammatory and anti-carcinoma properties. Long-chain bases (LCBs), the essential backbones of sphingolipids, are expected to be important for these bioactivities, and they vary structurally bet...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919070/ https://www.ncbi.nlm.nih.gov/pubmed/33648494 http://dx.doi.org/10.1186/s12944-021-01448-2 |
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author | Mikami, Daisuke Sakai, Shota Nishimukai, Megumi Yuyama, Kohei Mukai, Katsuyuki Igarashi, Yasuyuki |
author_facet | Mikami, Daisuke Sakai, Shota Nishimukai, Megumi Yuyama, Kohei Mukai, Katsuyuki Igarashi, Yasuyuki |
author_sort | Mikami, Daisuke |
collection | PubMed |
description | BACKGROUND: Dietary sphingolipids have various biofunctions, including skin barrier improvement and anti-inflammatory and anti-carcinoma properties. Long-chain bases (LCBs), the essential backbones of sphingolipids, are expected to be important for these bioactivities, and they vary structurally between species. Given these findings, however, the absorption dynamics of each LCB remain unclear. METHODS: In this study, five structurally different LCBs were prepared from glucosylceramides (GlcCers) with LCB 18:2(4E,8Z);2OH and LCB 18:2(4E,8E);2OH moieties derived from konjac tuber (Amorphophallus konjac), from GlcCers with an LCB 18(9Me):2(4E,8E);2OH moiety derived from Tamogi mushroom (Pleurotus cornucopiae var. citrinopileatus), and from ceramide 2-aminoethyphosphonate with LCB 18:3(4E,8E,10E);2OH moiety and LCB 18(9Me):3(4E,8E,10E);2OH moiety derived from giant scallop (Mizuhopecten yessoensis), and their absorption percentages and metabolite levels were analyzed using a lymph-duct-cannulated rat model via liquid chromatography tandem mass spectrometry (LC/MS/MS) with a multistage fragmentation method. RESULTS: The five orally administered LCBs were absorbed and detected in chyle (lipid-containing lymph) as LCBs and several metabolites including ceramides, hexosylceramides, and sphingomyelins. The absorption percentages of LCBs were 0.10–1.17%, depending on their structure. The absorption percentage of LCB 18:2(4E,8Z);2OH was the highest (1.17%), whereas that of LCB 18:3(4E,8E,10E);2OH was the lowest (0.10%). The amount of sphingomyelin with an LCB 18:2(4E,8Z);2OH moiety in chyle was particularly higher than sphingomyelins with other LCB moieties. CONCLUSIONS: Structural differences among LCBs, particularly geometric isomerism at the C8–C9 position, significantly affected the absorption percentages and ratio of metabolites. This is the first report to elucidate that the absorption and metabolism of sphingolipids are dependent on their LCB structure. These results could be used to develop functional foods that are more readily absorbed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-021-01448-2. |
format | Online Article Text |
id | pubmed-7919070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79190702021-03-02 Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph Mikami, Daisuke Sakai, Shota Nishimukai, Megumi Yuyama, Kohei Mukai, Katsuyuki Igarashi, Yasuyuki Lipids Health Dis Research BACKGROUND: Dietary sphingolipids have various biofunctions, including skin barrier improvement and anti-inflammatory and anti-carcinoma properties. Long-chain bases (LCBs), the essential backbones of sphingolipids, are expected to be important for these bioactivities, and they vary structurally between species. Given these findings, however, the absorption dynamics of each LCB remain unclear. METHODS: In this study, five structurally different LCBs were prepared from glucosylceramides (GlcCers) with LCB 18:2(4E,8Z);2OH and LCB 18:2(4E,8E);2OH moieties derived from konjac tuber (Amorphophallus konjac), from GlcCers with an LCB 18(9Me):2(4E,8E);2OH moiety derived from Tamogi mushroom (Pleurotus cornucopiae var. citrinopileatus), and from ceramide 2-aminoethyphosphonate with LCB 18:3(4E,8E,10E);2OH moiety and LCB 18(9Me):3(4E,8E,10E);2OH moiety derived from giant scallop (Mizuhopecten yessoensis), and their absorption percentages and metabolite levels were analyzed using a lymph-duct-cannulated rat model via liquid chromatography tandem mass spectrometry (LC/MS/MS) with a multistage fragmentation method. RESULTS: The five orally administered LCBs were absorbed and detected in chyle (lipid-containing lymph) as LCBs and several metabolites including ceramides, hexosylceramides, and sphingomyelins. The absorption percentages of LCBs were 0.10–1.17%, depending on their structure. The absorption percentage of LCB 18:2(4E,8Z);2OH was the highest (1.17%), whereas that of LCB 18:3(4E,8E,10E);2OH was the lowest (0.10%). The amount of sphingomyelin with an LCB 18:2(4E,8Z);2OH moiety in chyle was particularly higher than sphingomyelins with other LCB moieties. CONCLUSIONS: Structural differences among LCBs, particularly geometric isomerism at the C8–C9 position, significantly affected the absorption percentages and ratio of metabolites. This is the first report to elucidate that the absorption and metabolism of sphingolipids are dependent on their LCB structure. These results could be used to develop functional foods that are more readily absorbed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-021-01448-2. BioMed Central 2021-03-01 /pmc/articles/PMC7919070/ /pubmed/33648494 http://dx.doi.org/10.1186/s12944-021-01448-2 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Mikami, Daisuke Sakai, Shota Nishimukai, Megumi Yuyama, Kohei Mukai, Katsuyuki Igarashi, Yasuyuki Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph |
title | Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph |
title_full | Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph |
title_fullStr | Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph |
title_full_unstemmed | Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph |
title_short | Structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph |
title_sort | structure-dependent absorption of atypical sphingoid long-chain bases from digestive tract into lymph |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919070/ https://www.ncbi.nlm.nih.gov/pubmed/33648494 http://dx.doi.org/10.1186/s12944-021-01448-2 |
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