TY - JOUR T1 - Prolactin Upregulates Female-Predominant <em>P450</em> Gene Expressions and Downregulates Male-Predominant Gene Expressions in Mouse Liver JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 586 LP - 592 DO - 10.1124/dmd.116.074658 VL - 45 IS - 6 AU - Yuya Sato AU - Yoshikatsu Kaneko AU - Takamasa Cho AU - Kei Goto AU - Tadashi Otsuka AU - Suguru Yamamoto AU - Shin Goto AU - Hiroki Maruyama AU - Ichiei Narita Y1 - 2017/06/01 UR - http://dmd.aspetjournals.org/content/45/6/586.abstract N2 - Prolactin is a polypeptide hormone with over 300 separate biologic activities. Its serum level is increased during pregnancy and lactation, and it has been reported that pregnancy and lactation affect drug and steroid metabolism in mice and humans. Several studies reported that pregnancy or lactation influences liver cytochrome P450 (P450) expression and its activity, affecting the biosynthesis of steroids and xenobiotics through growth hormone or sex hormones; however, the role of prolactin as the regulator of liver P450 expression has not been elucidated so far. In the present study, we focused on prolactin as the regulator of expression of liver sex-predominant genes, including P450s. To investigate the role of prolactin in the hepatic gene expressions, pCAGGS expression vector containing mouse prolactin cDNA was transfected by hydrodynamic injection into both male and female mice. Hyperprolactinemia phosphorylated signal transducer and activator of transcription 5 in the liver and augmented female mouse liver mRNA expression of Cyp3a16, Cyp3a41, Cyp3a44, Cyp2b9, and prolactin receptor genes, whose expressions were female-predominant in hepatocytes. Moreover, liver expression of male-predominant genes such as Cyp2d9, Cyp7b1, Mup1, and Alas2 were reduced in male mice with hyperprolactinemia. The serum levels of conventional regulators of hepatic gene expressions, growth hormone, and testosterone were not affected by hyperprolactinemia. We demonstrated that prolactin upregulated female-predominant genes in female mice and downregulated male-predominant genes in male mice. We conjecture that higher concentration of prolactin would alter steroid and xenobiotic metabolisms by modulating hepatic P450 gene expressions during pregnancy and lactation. ER -