Title : Regulation of drug transporter gene expression by nuclear receptors.

Pub. Date : 2003 May

PMID : 12695338






6 Functional Relationships(s)
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1 Additionally, phenobarbital (PB)-inducible Oatp2 and Mrp3 gene expression was significantly increased in the PXR-KO mice when compared with wild-type PB-treated mice. Phenobarbital nuclear receptor subfamily 1, group I, member 2 Mus musculus
2 Additionally, phenobarbital (PB)-inducible Oatp2 and Mrp3 gene expression was significantly increased in the PXR-KO mice when compared with wild-type PB-treated mice. Phenobarbital nuclear receptor subfamily 1, group I, member 2 Mus musculus
3 Additionally, phenobarbital (PB)-inducible Oatp2 and Mrp3 gene expression was significantly increased in the PXR-KO mice when compared with wild-type PB-treated mice. Phenobarbital nuclear receptor subfamily 1, group I, member 2 Mus musculus
4 We also examined the effect of PXR ablation on PB-inducible hepatic CYP3A activity in vivo. Phenobarbital nuclear receptor subfamily 1, group I, member 2 Mus musculus
5 Microsomes isolated from PB-treated PXR-KO mice exhibited a significantly elevated rate of testosterone 6 beta-hydroxylation when compared with microsomes isolated from wild-type PB-treated mice. Phenobarbital nuclear receptor subfamily 1, group I, member 2 Mus musculus
6 PB treatment produced significantly increased levels of hepatomegaly in PXR-KO mice when compared with wild-type PB-treated mice. Phenobarbital nuclear receptor subfamily 1, group I, member 2 Mus musculus