Phenobarbital regulates nuclear expression of HNF-4α in mouse and rat Hepatocytes independent of CAR and PXR
Phenobarbital regulates nuclear expression of HNF-4α in mouse and rat Hepatocytes independent of CAR and PXR
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DOI：
10.1002/hep.21234
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发表时间：
2006-07-01
期刊：
影响因子：
13.5
通讯作者：
Michalopoulos, George K.
中科院分区：
文献类型：
--
作者：
Bell, Aaron W.;Michalopoulos, George K.
Phenobarbital is a lipophilic molecule used as a sedative and antiepileptic drug that elicits a multitude of effects in the liver, including gross liver enlargement, hepatocyte hypertrophy, and induced expression of drug-metabolizing enzymes and other liver-specific genes. The constitutive androstane receptor (CAR; NR1I3) and to a lesser extent the pregnane X receptor (PYCR; NR1I2) are responsible for mediating induction of many phenobarbital-responsive genes. However, CAR-mediated transcriptional control of some genes is critically dependent on hepatocyte nuclear factor 4 alpha (HNF-4 alpha; NR2A1), which itself regulates multiple liver-specific genes involved in hepatic growth, metabolism, and differentiation. We studied the effects of phenobarbital on HNF-4 alpha expression in hepatocytes and provide evidence that HNF-4 alpha nuclear expression is regulated in response to phenobarbital. Real-time polymerase chain reaction analyses revealed that HNF-4 alpha mRNA is modestly upregulated by phenobarbital. In addition, nuclear expression of HNF-4 alpha protein is significantly elevated 3 hours after the administration of phenobarbital in wild-type, CAR(-/-), and CAR(-/-)PXR(-/-) mice. In vitro analysis revealed that phenobarbital-induced HNF-4 alpha expression is both time- and dose dependent. In addition, the phosphatase inhibitor okadaic acid and the Ca2+/calmodulin-dependent protein kinase II inhibitor KN62 block nuclear induction of HNF-4 alpha by phenobarbital. Furthermore, HNF-4 alpha nuclear expression is enhanced by inhibition of cyclic AMP-dependent protein kinase A. In conclusion, induced nuclear expression of HNF-4 alpha and CAR is an integral part of the phenobarbital response, aimed at coordinated regulation of genes involved in drug metabolism and detoxification as well as maintenance of liver function.
