Kim Hyung-Sub, Saito Konomu, Ishizuka Mayumi, Kazusaka Akio, Fujita Shoichi
Laboratory of Toxicology, Department of Environmental Veterinary Sciences, Graduate School of Veterinary Medicine, Hokkaido University, N18, W9, Kita-ku, 060-0818 Sapporo, Japan.
Arch Toxicol. 2003 Aug;77(8):446-51. doi: 10.1007/s00204-003-0466-7. Epub 2003 Jun 27.
Exposure of pubertal rats to di-(2-ethylhexyl) phthalate (DEHP) for 14 days was reported to result in reduced testosterone (T) biosynthesis by altering androstenedione 17beta-hydroxysteroid dehydrogenase (17beta-HSD) activity. However, our study indicated that shorter period exposure of DEHP (100 or 1000 mg/kg for 5 days) to 4-week-old male rats did not affect the activity of 17beta-HSD, the rate-limiting enzyme of T biosynthesis in the testis. Testosterone 5alpha-reductase (T5alpha-R) activity in the testis was significantly enhanced, while aromatase mRNA was significantly reduced by increasing doses of DEHP. The expressions of cytochrome P450 (CYP) isoforms, CYP2C11 and CYP3A, in the testis increased along with their enzymatic activities, T16alpha- and T6beta-hydroxylation, respectively. Thus, the current study clearly indicates that the short period exposure to DEHP alters T metabolism through altering activities of T5alpha-R, aromatase and CYP2C11/3A2 in the testis of prepubertal rats, and that they are more sensitive marker enzymes to the DEHP exposure than those of biosynthetic enzymes of T from androstenedione.
据报道,青春期大鼠暴露于邻苯二甲酸二(2-乙基己基)酯(DEHP)14天会通过改变雄烯二酮17β-羟类固醇脱氢酶(17β-HSD)活性而导致睾酮(T)生物合成减少。然而,我们的研究表明,4周龄雄性大鼠短期暴露于DEHP(100或1000 mg/kg,持续5天)并不影响17β-HSD的活性,17β-HSD是睾丸中T生物合成的限速酶。随着DEHP剂量增加,睾丸中的睾酮5α-还原酶(T5α-R)活性显著增强,而芳香化酶mRNA显著减少。睾丸中细胞色素P450(CYP)同工型CYP2C11和CYP3A的表达分别随着它们的酶活性(T16α-和T6β-羟化)增加而增加。因此,当前研究清楚地表明,短期暴露于DEHP会通过改变青春期前大鼠睾丸中T5α-R、芳香化酶和CYP2C11/3A2的活性来改变T代谢,并且与从雄烯二酮合成T的酶相比,它们是对DEHP暴露更敏感的标记酶。