Gs. Reddy et al., Metabolism of 1 alpha,25-dihydroxyvitamin D-3 and its C-3 epimer 1 alpha,25-dihydroxy-3-epi-vitamin D-3 in neonatal human keratinocytes, STEROIDS, 66(3-5), 2001, pp. 441-450
We previously reported that 1 alpha ,25-dihydroxyvitamin D-3 [1 alpha ,25(O
H)(2)D-3] is metabolized into 1 alpha ,25-dihydroxy-3-epi-vitamin D-3 [1 al
pha ,25(OH)(2)-3-epi-D-3] in primary cultures of neonatal human keratinocyt
es. We now report that 1 alpha ,25(OH)(2)-3-epi-D-3 itself is further metab
olized in human keratinocytes into several polar metabolites. One of the po
lar metabolite was unequivocally identified as 1 alpha ,23,25-trihydroxy-3-
epi-vitamin D-3 by mass spectrometry and its sensitivity to sodium periodat
e. Three of the polar metabolites were identified as 1 alpha ,24,25-trihydr
oxy-3-epi-vitamin D-3, 1 alpha ,25-dihydroxy-24-oxo-3-epi-vitamin D-3 and 1
alpha ,23,25-trihydroxy-24-oxo-3-epi-vitamin D-3 by comigration with authe
ntic standards on both straight and reverse phase HPLC systems. In addition
to the polar metabolites, 1 alpha ,25(OH)(2)-3-epi-D-3 was also metabolize
d into two less polar metabolites. A possible structure of either 1 alpha O
H-3-epi-D-3-20,25-cyclic ether or 1 alpha OH-3-epi-D-3-24,25-epoxide was as
signed to one of the less polar metabolites through mass spectrometry. Thus
, we indicate for the first time that 1 alpha ,25(OH)(2)-3-epi-D-3 is metab
olized in neonatal human keratinocytes not only via the same C-24 and C-23
oxidation pathways like its parent, 1 alpha ,25(OH)(2)D-3; but also is meta
bolized into a less polar metabolite via a pathway that is unique to 1 alph
a ,25(OH)(2)-3-epi-D-3. (C) 2001 Elsevier Science Inc. All rights reserved.