Abstract:
:Male Wistar rats were treated with 50 mg 3,3',4,4'-tetrachlorobiphenyl (TCB)/kg BW or vehicle. After 4 days, the livers were isolated and perfused for 90 min with 2 nM [125I]T3 or 10 nM [125I]T4 in Krebs-Ringer medium containing 1% albumin. Deiodination and conjugation products and remaining substrates were determined in bile and medium samples by Sephadex LH-20 chromatography and HPLC. TCB treatment did not affect hepatic uptake and metabolism of T3. However, biliary excretion of T4 glucuronide was strongly increased by TCB, resulting in an augmented T4 disappearance from the medium, although initial hepatic uptake of T4 was not altered. Measurement of the microsomal UDP-glucuronyltransferase (UDPGT) activities confirmed that T4 UDPGT was induced by TCB, whereas T3 glucuronidation was unaffected. T3 UDPGT activity showed a discontinuous variation, which completely matched the genetic heterogeneity in androsterone glucuronidation in Wistar rats. These results indicate that different isozymes catalyze the glucuronidation of T3 and T4.
journal_name
Endocrinologyjournal_title
Endocrinologyauthors
Beetstra JB,van Engelen JG,Karels P,van der Hoek HJ,de Jong M,Docter R,Krenning EP,Hennemann G,Brouwer A,Visser TJdoi
10.1210/endo-128-2-741subject
Has Abstractpub_date
1991-02-01 00:00:00pages
741-6issue
2eissn
0013-7227issn
1945-7170journal_volume
128pub_type
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