DeGroot L J, Rue P A
J Clin Endocrinol Metab. 1979 Oct;49(4):538-42. doi: 10.1210/jcem-49-4-538.
The ability of roentgenographic contrast agents to inhibit binding of [125I]T3 to nuclear receptors was studied during incubation of rat liver nuclei or nuclear extracts in vitro and after ip administration of the agents in vivo. Ipodate, iodipamide, iopanoic acid, and diatrizoate inhibited binding of [125I]T3 in vitro. The most potent inhibitor was ipodate, which produced 50% inhibition of binding at 1.2 X 10(-4) M. When given orally in acute in vivo experiments, ipodate did not diminish binding to liver nuclear receptors. Ipodate appeared to inhibit in vivo metabolism of [125I]T3.
在体外培养大鼠肝细胞核或核提取物以及体内腹腔注射造影剂后,研究了X线造影剂抑制[125I]T3与核受体结合的能力。碘番酸、碘他拉酸、碘帕醇和泛影葡胺在体外抑制[125I]T3的结合。最强的抑制剂是碘番酸,在1.2×10(-4)M时产生50%的结合抑制。在急性体内实验中口服碘番酸时,它不会减少与肝细胞核受体的结合。碘番酸似乎抑制了[125I]T3的体内代谢。