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Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey
20(S)-Hydroxyvitamin D3 (20(OH)D3) is an endogenous metabolite produced by the action of CYP11A1 on the side chain of vitamin D3 (D3). 20(OH)D3 can be further hydroxylated by CYP11A1, CYP27A1, CYP24A1 and/or CYP27B1 to several hydroxyderivatives. CYP11A1 also hydroxylates D3 to 22-monohydroxyvitamin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321140/ https://www.ncbi.nlm.nih.gov/pubmed/32498437 http://dx.doi.org/10.3390/molecules25112583 |
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author | Kim, Tae-Kang Atigadda, Venkatram Brzeminski, Pawel Fabisiak, Adrian Tang, Edith K. Y. Tuckey, Robert C. Slominski, Andrzej T. |
author_facet | Kim, Tae-Kang Atigadda, Venkatram Brzeminski, Pawel Fabisiak, Adrian Tang, Edith K. Y. Tuckey, Robert C. Slominski, Andrzej T. |
author_sort | Kim, Tae-Kang |
collection | PubMed |
description | 20(S)-Hydroxyvitamin D3 (20(OH)D3) is an endogenous metabolite produced by the action of CYP11A1 on the side chain of vitamin D3 (D3). 20(OH)D3 can be further hydroxylated by CYP11A1, CYP27A1, CYP24A1 and/or CYP27B1 to several hydroxyderivatives. CYP11A1 also hydroxylates D3 to 22-monohydroxyvitamin D3 (22(OH)D3), which is detectable in the epidermis. 20-Hydroxy-7-dehydrocholesterol (20(OH)-7DHC) has been detected in the human epidermis and can be phototransformed into 20(OH)D3 following the absorption of ultraviolet B (UVB) energy by the B-ring. 20(OH)D3 and its hydroxyderivatives have anti-inflammatory, pro-differentiation and anti-proliferative effects, comparable to 1,25-dihydroxyvitamin D3 (1,25(OH)(2)D3). Since cytochromes P450 with 20- or 25-hydroxylase activity are found in insects participating in ecdysone synthesis from 7-dehydrocholesterol (7DHC), we tested whether D3-hydroxyderivatives are present in honey, implying their production in bees. Honey was collected during summer in the Birmingham area of Alabama or purchased commercially and extracted and analyzed using LC-MS. We detected a clear peak of m/z = 423.324 [M + Na](+) for 20(OH)D3 corresponding to a concentration in honey of 256 ng/g. We also detected peaks of m/z = 383.331 [M + H − H(2)O](+) for 20(OH)-7DHC and 25(OH)D3 with retention times corresponding to the standards. We further detected species with m/z = 407.329 [M + Na](+) corresponding to the RT of 7DHC, D3 and lumisterol3 (L3). Similarly, peaks with m/z = 399.326 [M + H − H(2)O](+) were detected at the RT of 1,25(OH)(2)D3 and 1,20-dihydroxyvitamin D3 (1,20(OH)(2)D3). Species corresponding to 20-monohydroxylumisterol3 (20(OH)L3), 22-monohydroxyvitamin D3 (22(OH)D3), 20,23-dihydroxyvitamin D3 (20,23(OH)(2)D3), 20,24/25/26-dihydroxyvitamin D3 (20,24/25/26(OH)(2)D3) and 1,20,23/24/25/26-trihydroxyvitamin D3 (1,20,23/24/25/26(OH)(3)D3) were not detectable above the background. In conclusion, the presence of 7DHC and D3 and of species corresponding to 20(OH)-7DHC, 20(OH)D3, 1,20(OH)(2)D3, 25(OH)D3 and 1,25(OH)(2)D3 in honey implies their production in bees, although the precise biochemistry and photochemistry of these processes remain to be defined. |
format | Online Article Text |
id | pubmed-7321140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73211402020-07-06 Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey Kim, Tae-Kang Atigadda, Venkatram Brzeminski, Pawel Fabisiak, Adrian Tang, Edith K. Y. Tuckey, Robert C. Slominski, Andrzej T. Molecules Article 20(S)-Hydroxyvitamin D3 (20(OH)D3) is an endogenous metabolite produced by the action of CYP11A1 on the side chain of vitamin D3 (D3). 20(OH)D3 can be further hydroxylated by CYP11A1, CYP27A1, CYP24A1 and/or CYP27B1 to several hydroxyderivatives. CYP11A1 also hydroxylates D3 to 22-monohydroxyvitamin D3 (22(OH)D3), which is detectable in the epidermis. 20-Hydroxy-7-dehydrocholesterol (20(OH)-7DHC) has been detected in the human epidermis and can be phototransformed into 20(OH)D3 following the absorption of ultraviolet B (UVB) energy by the B-ring. 20(OH)D3 and its hydroxyderivatives have anti-inflammatory, pro-differentiation and anti-proliferative effects, comparable to 1,25-dihydroxyvitamin D3 (1,25(OH)(2)D3). Since cytochromes P450 with 20- or 25-hydroxylase activity are found in insects participating in ecdysone synthesis from 7-dehydrocholesterol (7DHC), we tested whether D3-hydroxyderivatives are present in honey, implying their production in bees. Honey was collected during summer in the Birmingham area of Alabama or purchased commercially and extracted and analyzed using LC-MS. We detected a clear peak of m/z = 423.324 [M + Na](+) for 20(OH)D3 corresponding to a concentration in honey of 256 ng/g. We also detected peaks of m/z = 383.331 [M + H − H(2)O](+) for 20(OH)-7DHC and 25(OH)D3 with retention times corresponding to the standards. We further detected species with m/z = 407.329 [M + Na](+) corresponding to the RT of 7DHC, D3 and lumisterol3 (L3). Similarly, peaks with m/z = 399.326 [M + H − H(2)O](+) were detected at the RT of 1,25(OH)(2)D3 and 1,20-dihydroxyvitamin D3 (1,20(OH)(2)D3). Species corresponding to 20-monohydroxylumisterol3 (20(OH)L3), 22-monohydroxyvitamin D3 (22(OH)D3), 20,23-dihydroxyvitamin D3 (20,23(OH)(2)D3), 20,24/25/26-dihydroxyvitamin D3 (20,24/25/26(OH)(2)D3) and 1,20,23/24/25/26-trihydroxyvitamin D3 (1,20,23/24/25/26(OH)(3)D3) were not detectable above the background. In conclusion, the presence of 7DHC and D3 and of species corresponding to 20(OH)-7DHC, 20(OH)D3, 1,20(OH)(2)D3, 25(OH)D3 and 1,25(OH)(2)D3 in honey implies their production in bees, although the precise biochemistry and photochemistry of these processes remain to be defined. MDPI 2020-06-02 /pmc/articles/PMC7321140/ /pubmed/32498437 http://dx.doi.org/10.3390/molecules25112583 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Tae-Kang Atigadda, Venkatram Brzeminski, Pawel Fabisiak, Adrian Tang, Edith K. Y. Tuckey, Robert C. Slominski, Andrzej T. Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey |
title | Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey |
title_full | Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey |
title_fullStr | Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey |
title_full_unstemmed | Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey |
title_short | Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey |
title_sort | detection of 7-dehydrocholesterol and vitamin d3 derivatives in honey |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321140/ https://www.ncbi.nlm.nih.gov/pubmed/32498437 http://dx.doi.org/10.3390/molecules25112583 |
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