Comparative study on 2,2',4,5,5'-pentachlorobiphenyl-mediated decrease in serum thyroxine level between C57BL/6 and its transthyretin-deficient mice.

The relationships between the changes in the levels of serum total thyroxine (T4), serum T4-transthyretin (TTR) complex, and accumulation of T4 in tissues by 2,2′,4,5,5′-pentachlorobiphenyl (PentaCB) were examined using wild-type C57BL/6 (WT) and its TTR-deficient (TTR-null) mice. The constitutive level of serum total T4 was much higher in WT mice than in TTR-null mice. In WT mice 4days after a single intraperitoneal injection with PentaCB (112mg/kg), serum total T4 level was significantly decreased along with a decrease in serum T4–TTR complex, and the levels of serum total T4 in the PentaCB-treated WT mice were almost the same to those in PentaCB-untreated (control) TTR-null mice. In addition, a slight decrease in serum total T4 by PentaCB treatment was observed in TTR-null mice. Furthermore, clearance of [125I]T4 from the serum after [125I]T4-administration was promoted by the PentaCB-pretreatment in either strain of mice, especially WT mice. On the other hand, accumulation level of [125I]T4 in the liver, but not in extrahepatic tissues, was strikingly enhanced in the PentaCB-pretreated WT and TTR-null mice. Furthermore, in both strains of mice, PentaCB-pretreatment led to significant increases in the steady-state distribution volume of [125I]T4 and the concentration ratio of the liver to serum. The present findings demonstrate that PentaCB-mediated decrease in serum T4 level occurs mainly through increase in accumulation level of T4 in the liver and further indicate that the increased accumulation of T4 in the liver of WT mice is primarily dependent on the PentaCB-mediated inhibition of serum T4–TTR complex formation.