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   <subfield code="a">The Generation of C-3α Epimer of 25-Hydroxyvitamin D and Its Biological Effects on Bone Mineral Density in Adult Rodents</subfield>
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   <subfield code="c">[Christina Bianchini, Paula Lavery, Sherry Agellon, Hope Weiler]</subfield>
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   <subfield code="a">The source and function of C-3α epimer of 25(OH)D (C-3 epimer) is unknown. The objectives were to (1) establish if increasing doses of vitamin D (VD) results in a proportionate dose-response in C-3 epimer; and (2) determine the biological response of bone to C-3 epimer treatment. Sprague Dawley rats (12weeks, n=36 female, n=36 male) were randomized to control AIN93-M diet (1IU VD3/g diet) or an experimental diet for 8weeks containing VD3 at 2 or 4IU/g diet, C-3 epimer at 0.5 or 1IU/g diet or 25(OH)D (0.5IU/g diet). BW and food consumption were measured weekly. Blood was sampled at week 0, 4, and 8 for assessment of VD metabolites and bone metabolism biomarkers. DXA (week 0, 4, and 8) and in vivo micro CT (μCT) (week 0 and 8) were performed in vivo plus ex vivo μCT imaging and bone biomechanics. Dietary intake and anthropometry did not differ among diet groups. The dose-response of VD generated significantly elevated C-3 epimer only in females with concentrations of 4IU VD diet group [mean 84.6 (62.5)nmol/L] exceeding control [mean 21.4 (18.5)nmol/L, p=0.005]. Both sexes in the 25(OH)D group did not show significant increases in C-3 epimer, whereas 0.5 and 1IU epimer groups exceeded 100nmol/L of C-3 epimer by 8weeks. These data suggest C-3 epimer is endogenously generated with higher intakes of VD. Endogenous and exogenous C-3 epimer accumulates in serum without impact upon bone health outcomes in a healthy young adult model over 8weeks.</subfield>
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   <subfield code="a">Vitamin D</subfield>
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