Wieneke N, Neuschäfer-Rube F, Bode L M, Kuna M, Andres J, Carnevali L C, Hirsch-Ernst K I, Püschel G P
University of Potsdam, Institute of Nutrition Science, Biochemistry of Nutrition, Arthur-Scheunert-Allee 114-116, D14558 Nuthetal, Germany.
Toxicol Appl Pharmacol. 2009 Oct 1;240(1):99-107. doi: 10.1016/j.taap.2009.07.014. Epub 2009 Jul 22.
Energy balance is maintained by controlling both energy intake and energy expenditure. Thyroid hormones play a crucial role in regulating energy expenditure. Their levels are adjusted by a tight feedback-controlled regulation of thyroid hormone production/incretion and by their hepatic metabolism. Thyroid hormone degradation has previously been shown to be enhanced by treatment with phenobarbital or other antiepileptic drugs due to a CAR-dependent induction of phase II enzymes of xenobiotic metabolism. We have recently shown, that PPAR alpha agonists synergize with phenobarbital to induce another prototypical CAR target gene, CYP2B1. Therefore, it was tested whether a PPAR alpha agonist could enhance the phenobarbital-dependent acceleration of thyroid hormone elimination. In primary cultures of rat hepatocytes the apparent half-life of T3 was reduced after induction with a combination of phenobarbital and the PPAR alpha agonist WY14643 to a larger extent than after induction with either compound alone. The synergistic reduction of the half-life could be attributed to a synergistic induction of CAR and the CAR target genes that code for enzymes and transporters involved in the hepatic elimination of T3, such as OATP1A1, OATP1A3, UGT1A3 and UGT1A10. The PPAR alpha-dependent CAR induction and the subsequent induction of T3-eliminating enzymes might be of physiological significance for the fasting-induced reduction in energy expenditure by fatty acids as natural PPAR alpha ligands. The synergism of the PPAR alpha agonist WY14643 and phenobarbital in inducing thyroid hormone breakdown might serve as a paradigm for the synergistic disruption of endocrine control by other combinations of xenobiotics.
能量平衡通过控制能量摄入和能量消耗来维持。甲状腺激素在调节能量消耗中起关键作用。它们的水平通过对甲状腺激素产生/分泌的严格反馈控制调节以及肝脏代谢来调节。先前已表明,由于CAR依赖性诱导外源性代谢的II相酶,用苯巴比妥或其他抗癫痫药物治疗可增强甲状腺激素降解。我们最近发现,PPARα激动剂与苯巴比妥协同作用可诱导另一个典型的CAR靶基因CYP2B1。因此,测试了PPARα激动剂是否能增强苯巴比妥依赖性的甲状腺激素消除加速作用。在大鼠肝细胞原代培养物中,用苯巴比妥和PPARα激动剂WY14643联合诱导后,T3的表观半衰期比单独用任何一种化合物诱导后降低的程度更大。半衰期的协同降低可归因于CAR及其靶基因的协同诱导,这些靶基因编码参与肝脏消除T3的酶和转运蛋白,如OATP1A1、OATP1A3、UGT1A3和UGT1A10。PPARα依赖性的CAR诱导以及随后T3消除酶的诱导对于脂肪酸作为天然PPARα配体在禁食诱导的能量消耗减少中可能具有生理意义。PPARα激动剂WY14643与苯巴比妥在诱导甲状腺激素分解方面的协同作用可能作为外源性物质其他组合对内分泌控制协同破坏的范例。