A new in vivo analysis model to detect sexually dimorphic rat liver cytochrome P450 gene expression dependent on growth hormone secretory patterns

• Published in: Experimental Animals Vol. 65; no. 4; pp. 447 - 454
• Main Authors: Maruyama, Motoyo, Fujisawa, Masahiko, Yokosuka, Makoto, Saito, Toru R., Hayama, Shin-ichi, Akimoto, Toshio, Hakamata, Yoji
• Format: Journal Article
• Language: English
• Published: Japan Japanese Association for Laboratory Animal Science 2016
• Subjects: Animals; Aryl Hydrocarbon Hydroxylases - genetics; Aryl Hydrocarbon Hydroxylases - metabolism; cytochrome P450; Cytochrome P450 Family 2 - genetics; Cytochrome P450 Family 2 - metabolism; Female; Gene Expression; Growth Hormone - metabolism; in vivo imaging; Liver - metabolism; Luminescent Proteins - chemistry; Male; Models, Animal; Original; Rats; Rats, Transgenic; Rats, Wistar; Red Fluorescent Protein; RNA, Messenger - metabolism; Sex Characteristics; sexual dimorphism; Steroid 16-alpha-Hydroxylase - genetics; Steroid 16-alpha-Hydroxylase - metabolism; Steroid Hydroxylases - genetics; Steroid Hydroxylases - metabolism; transgenic rat
• ISSN: 1341-1357; 1881-7122
• DOI: 10.1538/expanim.16-0030

Several drug-metabolizing cytochrome P450 (CYP) enzymes exhibit sexual dimorphism depending on the pituitary growth hormone (GH) secretory patterns. However, the mechanism underlying CYP sexual dimorphism remains unclear. We previously established a transgenic (Alb-DsRed2 Tg) rat that expressed red fluorescent DsRed2 protein, particularly in hepatocytes, to visualize cell differentiation and multiplication and found that hepatic DsRed2 expression exhibited sexual dimorphism that was limited to adult males. In this study, we compared the expression patterns between sexual dimorphic Cyps and DsRed2 in Tg rats after experimentally reversing the GH secretory patterns in males and females. Postnatal day 1 male and female Tg rats were gonadectomized and then testosterone propionate (0.25 mg/rat) was subcutaneously administered to ovariectomized females immediately after surgery. Cyp mRNA and DsRed2 expression levels were quantified using RT-PCR and an in vivo imaging system, respectively. GH-dependent Cyps and hepatic DsRed2 expression patterns were reversed in males and females at 9 weeks after birth and were significantly correlated (P<0.05). This suggested that DsRed2 expression in these Tg rats depended on GH secretory patterns. Based on DsRed2 fluorescence, this Tg rat model could become a tool to readily and effectively evaluate changes in GH-dependent Cyp expression.