| Literature DB >> 17639023 |
Yoshihisa Kato1, Shin-ichi Ikushiro, Rie Takiguchi, Koichi Haraguchi, Nobuyuki Koga, Shinya Uchida, Toshiyuki Sakaki, Shizuo Yamada, Jun Kanno, Masakuni Degawa.
Abstract
We have previously suggested that the decrease in the levels of serum total thyroxine (T(4)) and free T(4) by a single administration to rats of Kanechlor-500 (KC500) at a dose of 100 mg/kg is not necessarily dependent on the increase in hepatic T(4)-UDP-glucuronosyltransferase (UDP-GT). In the present study, we determined whether or not a consecutive treatment with KC500 at a relatively low dose (10 mg/kg i.p., once daily for 10 days) results in a decrease in the level of serum total T(4) and further investigated an exact mechanism for the KC500-induced decrease in the T(4). At 4 days after final treatment with KC500, the serum total T(4) and free T(4) levels were markedly decreased in both Wistar and UGT1A-deficient Wistar (Gunn) rats, whereas significant increases in hepatic T(4)-UDP-GT activity were observed in Wistar rats but not in Gunn rats. The level of serum thyroid-stimulating hormone was not significantly changed in either Wistar or Gunn rats. Clearance from serum of the [(125)I]T(4) administered to the KC500-pretreated Wistar and Gunn rats was faster than that to the corresponding control (KC500-untreated) rats. The accumulated level of [(125)I]T(4) was increased in several tissues, especially the liver, in the KC500-pretreated rats. The present findings demonstrated that a consecutive treatment with KC500 resulted in a significant decrease in the level of serum total T(4) in both Wistar and Gunn rats and further indicated that the KC500-induced decrease would occur through increase in accumulation of T(4) in several tissues, especially the liver, rather than increase in hepatic T(4)-UDP-GT activity.Entities:
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Year: 2007 PMID: 17639023 DOI: 10.1124/dmd.107.017327
Source DB: PubMed Journal: Drug Metab Dispos ISSN: 0090-9556 Impact factor: 3.922