In vitro metabolism of thyroxine by rat and human hepatocytes. (30th October 2013)

• Record Type: Journal Article
• Authors: Richardson, Vicki M.; Ferguson, Stephen S.; Sey, Yusupha M.; DeVito, Michael J.
• Is Part Of: Xenobiotica. Volume 44:Number 5(2014:May)
• Page Start: 391
• Page End: 403
• Publication Date: 2013-10-30
• Subjects: Deiodination -- glucuronidation -- PCB 153 -- sulfation -- thyroid hormone -- T4; Metabolism -- Periodicals; Drugs -- Physiological effect -- Periodicals; Food additives -- Periodicals; Chemicals -- Physiological effect -- Periodicals; Biochemistry -- Periodicals; Pharmaceutical Preparations -- metabolism -- Periodicals; Metabolism -- Periodicals; 574.133
• DOI: 10.3109/00498254.2013.847990
• Languages: English
• ISSNs: 0049-8254

Abstract

Abstract: 1. The liver metabolizes thyroxine (T4 ) through two major pathways: deiodination and conjugation. Following exposure to xenobiotics, T4 conjugation increases through the induction of hepatic uridine diphosphate glucuronosyltransferase (UGT) in rodents; however, it is uncertain to what degree different species employ deiodination and conjugation in the metabolism of T4 . The objective of this study was to compare the metabolism of T4 in untreated and 2, 2′, 4, 4′, 5, 5′-hexachlorobiphenyl (PCB 153)-treated primary sandwich-cultured hepatocytes from rat (SCRH) and human (SCHH). 2. Basal metabolite concentrations were 13 times higher in the medium of SCRH compared to SCHH. Metabolite distribution in the medium of SCRH versus SCHH was as follows: T4 G, (91.6 versus 5.3%); T4 S, (3.6 versus 4.4%) and T3 + rT3, (4.9 versus 90.3%). PCB 153 induced T4 G in the medium of SCRH and SCHH; however, T4 S and T3 + rT3 were changed but to a much lesser degree. 3. The results indicate that baseline T4 glucuronidation is greater in SCRH compared to SCHH. These data also suggest that glucuronidation may be a more important pathway for T4 metabolism in rats and deiodination may be a favored pathway in humans; however, with PCB 153 treatment these data support glucuronidation as a primary route of T4 metabolism in both rat and humans.