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. Author manuscript; available in PMC: 2009 Jun 1.
Published in final edited form as: J Steroid Biochem Mol Biol. 2008 Apr 22;110(3-5):269–277. doi: 10.1016/j.jsbmb.2007.11.007

Figure 5.

Figure 5

Effects of N-benzyl-1α,25-(OH)2D3-26,23-lactam analogues and N-phenetyl-1α,25-(OH)2D3-26,23-lactam analogues on 25-OH-D3-24-hydroxylase gene expression induced by 1α,25-(OH)2D3 in HL-60 cells (A), human osteoblastic cell line (HOS cells) (B) and primary mouse osteoblastic cells (C). The experimental procedures for gene expression induced by vitamin D analogues were carried out as described in Materials and Methods. 1, vehicle; 2, 10−8M 1α,25-(OH)2D3; 3, 10−6M TEI-9647; 4, 10−6M (23S,25S)-DLAM-1P; 5, 10−6M (23S,25R)-DLAM-1P; 6, 10−6M (23S,25S)-DLAM-2P; 7, 10−6M (23S,25R)-DLAM-2P; 8, 10−6M 1α,25-(OH)2D3-26,23-lactone; 9, 10−8M 1α,25-(OH)2D3 + 10−6M TEI-9647; 10, 10−8M 1α,25-(OH)2D3 + 10−6M (23S,25S)-DLAM-1P; 11, 10−8M 1α,25-(OH)2D3 + 10−6M (23S,25R)-DLAM-1P; 12, 10−8M 1α,25-(OH)2D3 + 10−6M (23S,25S)-DLAM-2P; 13, 10−8M 1α,25-(OH)2D3 + 10−6M (23S,25R)-DLAM-2P; 14, 10−8M 1α,25-(OH)2D3 + 10−6M 1α,25-(OH)2D3-26,23-lactone. Similar results were seen in two independent experiments.