Protein-binding properties of 22-oxa-1 alpha,25-dihydroxyvitamin D3, a synthetic analogue of 1 alpha,25-dihydroxyvitamin D3

J Nutr Sci Vitaminol (Tokyo). 1989 Oct;35(5):529-33. doi: 10.3177/jnsv.35.529.

Abstract

Protein binding properties of 22-oxa-1 alpha,25-dihydroxyvitamin D3 (22-oxa-1,25-D3), a synthetic analogue of 1 alpha,25-dihydroxyvitamin D3 (1,25-D3), were compared with those of vitamin D3 derivatives. The order of binding affinity to the chick embryonic intestinal receptor was 1,25-D3 greater than 22-oxa-1,25-D3 greater than 25-hydroxyvitamin D3 (25-D3) greater than 24R, 25-dihydroxyvitamin D3 (24, 25-D3) greater than vitamin D3 (D3), while that to the rat plasma vitamin D-binding protein (DBP) was 25-D3 greater than 24,25-D3 greater than D3 greater than 1,25-D3 greater than 22-oxa-1,25-D3. The binding potencies of 22-oxa-1,25-D3 to the receptor and DBP were about 1/8 and 1/600 of the respective values of 1,25-D3. When the distribution of the tritiated compounds in human plasma components was examined by an in vitro polyacrylamide gel electrophoretic method, [3H]-22-oxa-1,25-D3 was found to bind only to the lipoproteins including chyromicron. These results suggest that the replacement of a carbon atom into an oxygen atom in the side chain structure of 1,25-D3 results significant decrease in the binding affinity to DBP and that 22-oxa-1,25-D3 is transported as a complex-form not with DBP but with lipoprotein to the target tissues.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Binding, Competitive
  • Calcitriol / analogs & derivatives
  • Calcitriol / blood
  • Calcitriol / metabolism*
  • Chick Embryo
  • Humans
  • In Vitro Techniques
  • Kinetics
  • Receptors, Cell Surface / metabolism*
  • Vitamin D Deficiency / metabolism*
  • Vitamin D-Binding Protein / blood
  • Vitamin D-Binding Protein / metabolism*

Substances

  • Receptors, Cell Surface
  • Vitamin D-Binding Protein
  • Calcitriol
  • maxacalcitol