Abstract
In rats, clofibrate acts as a microsomal enzyme inducer and disrupts the metabolism of thyroid hormones by increasing hepatic glucuronidation of thyroxine. Whether similar effects occur in the pig has not yet been investigated. This study was performed to investigate the effect of clofibrate treatment on metabolism of thyroid hormones in pigs. To this end, an experiment with 18 pigs, which were assigned to two groups, was performed. One group received a control diet, and the other group was fed the same diet supplemented with 5 g of clofibrate/kg for 28 days. Pigs treated with clofibrate had higher hepatic activities of T3- and T4-UDP glucuronosyltransferases (UGT) and lower concentrations of total and free T4 and total T3 in plasma than control pigs (P < 0.05). Weights and histology of the thyroid gland (epithelial height, follicle lumen diameter) did not differ between the two groups, but pigs treated with clofibrate had higher mRNA concentrations of various genes in the thyroid responsive to thyroid-stimulating hormone (TSH) such as TSH receptor, sodium iodine symporter, thyroid peroxidase, and cathepsin B than control pigs (P < 0.05). Pigs treated with clofibrate also had lower hepatic mRNA concentrations of proteins involved in plasma thyroid hormone transport [thyroxine-binding globulin (P < 0.10), transthyretin (P < 0.05), and albumin (P < 0.05)] and thyroid hormone receptor α1 (P < 0.05) than control pigs. In conclusion, this study shows that clofibrate treatment induces a strong activation of T3- and T4-UGT in pigs, leading to increased glucuronidation and markedly reduced plasma concentrations of these hormones, accompanied by a moderate stimulation of thyroid function.
Footnotes
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Article, publication date, and citation information can be found at http://dmd.aspetjournals.org.
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doi:10.1124/dmd.106.011379.
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ABBREVIATIONS: PPARα, peroxisome proliferator-activated receptor α; UGT, UDP glucuronosyltransferase(s); T4, thyroxine; T3, 3,3′,5-triiodothyronine; TSH, thyroid-stimulating hormone; pNP, p-nitrophenol; UDPGA, UDP-glucuronic acid; RT-PCR, reverse transcriptase polymerase chain reaction; GAPDH, glycerinaldehyde-3-phosphate dehydrogenase; ACO, acyl CoA oxidase; CPT-1, carnitine palmitoyl transferase 1.
- Received June 7, 2006.
- Accepted August 4, 2006.
- The American Society for Pharmacology and Experimental Therapeutics
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