Back to Search Start Over

Detection of 7-Dehydrocholesterol and Vitamin D3 Derivatives in Honey.

Authors :
Kim TK
Atigadda V
Brzeminski P
Fabisiak A
Tang EKY
Tuckey RC
Slominski AT
Source :
Molecules (Basel, Switzerland) [Molecules] 2020 Jun 02; Vol. 25 (11). Date of Electronic Publication: 2020 Jun 02.
Publication Year :
2020

Abstract

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) <subscript>2</subscript> 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] <superscript>+</superscript> 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 <subscript>2</subscript> O] <superscript>+</superscript> 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] <superscript>+</superscript> corresponding to the RT of 7DHC, D3 and lumisterol3 (L3). Similarly, peaks with m/z = 399.326 [M + H - H <subscript>2</subscript> O] <superscript>+</superscript> were detected at the RT of 1,25(OH) <subscript>2</subscript> D3 and 1,20-dihydroxyvitamin D3 (1,20(OH) <subscript>2</subscript> D3). Species corresponding to 20-monohydroxylumisterol3 (20(OH)L3), 22-monohydroxyvitamin D3 (22(OH)D3), 20,23-dihydroxyvitamin D3 (20,23(OH) <subscript>2</subscript> D3), 20,24/25/26-dihydroxyvitamin D3 (20,24/25/26(OH) <subscript>2</subscript> D3) and 1,20,23/24/25/26-trihydroxyvitamin D3 (1,20,23/24/25/26(OH) <subscript>3</subscript> 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) <subscript>2</subscript> D3, 25(OH)D3 and 1,25(OH) <subscript>2</subscript> D3 in honey implies their production in bees, although the precise biochemistry and photochemistry of these processes remain to be defined.

Details

Language :
English
ISSN :
1420-3049
Volume :
25
Issue :
11
Database :
MEDLINE
Journal :
Molecules (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
32498437
Full Text :
https://doi.org/10.3390/molecules25112583