Abstract
Two fractions which elute similarly as 1,25(OH)2D3 and 1,24,25(OH)3D3 were isolated by TLC, Sephadex LH-20 chromatog-raphy and HPLC from Solanum malacoxylon leaf extracts preincubated in vitro with ruminal fluid. Both fractions effectively competed with [3
H]-1,25(OH)2D3 for binding to the chick intestinal 1,25(OH)2D3 receptor. Only significant amounts of the fraction which coelutes with 1,25(OH)2D3 were detected in leaf extracts incubated with purified β-glucosidase. Incubation of [3
H]-1,25(OH)2D3 with ruminai fluid resulted in the formation of a metabolite with similar mobility as 1,24,25(OH)3D3 in TLC plates. The results suggest that 1,25(OH)2D3-glycoside present in S. malacoxylon is converted to 1,25 (OH)2D3 and a more polar metabolite, possibly 1,24,25(OH)3D3, by the action of rumen microbes.