In utero exposure to mono-N-butyl phthalate impairs insulin-like factor 3 gene expression and the transabdominal phase of testicular descent in fetal rats

被引:28
作者
Shono, T [1 ]
Shima, Y [1 ]
Kondo, T [1 ]
Suita, S [1 ]
机构
[1] Kyushu Univ, Dept Pediat Surg Reprod & Dev Med, Grad Sch Med Sci, Fukuoka 8128582, Japan
关键词
undescended testis; phthalate ester; INSL3; rat;
D O I
10.1016/j.jpedsurg.2005.08.027
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: Phthalate esters have been shown to cause Undescended testes (UT) in rats. It has been proposed that Leydig insulin-like factor 3 (INSL3) may play all important role in testicular descent. The aim of this study was to investigate the effect Of mono-N-butyl phthalate (MBP) on both t he INSL3 gene expression and the transabdominal testicular descent in rats. Methods: On the 19th gestational day, the male fetuses that had been exposed to MBP on the 15th to 18th gestational days were dissected and the degree of testicular ascent was examined. Next, quantitative reverse transcriptase polymerase chain reaction Was performed to analyze the testicular INSL3 gene expression. At 60 days of age, the testicular position was recorded in the rest of MBP-treated male offspring. Results: Oil the 19th gestational day, INSL3 messenger RNA expression was significantly decreased in the MBP-treated testes, and the associated degree of testicular ascent was significantly higher than in the controls. At 60 days of age, 12 (54.5%) of 22 rats had either unilateral or bilateral UT. Conclusions: Prenatal MBP may inhibit the INSL3 gene expression associated with the transabdominal testicular ascent in fetal rats, thereby causing UT in postnatal offspring. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1861 / 1864
页数:4
相关论文
共 24 条
[1]   The overexpression of the Insl3 in female mice causes descent of the ovaries [J].
Adham, IM ;
Steding, G ;
Thamm, T ;
Büllesbach, EE ;
Schwabe, C ;
Paprotta, I ;
Engel, W .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (02) :244-252
[2]   Relaxin-like factor (RLF) serum concentrations and gubernaculum RLF receptor display in relation to pre- and neonatal development of rats [J].
Boockfor, FR ;
Fullbright, G ;
Büllesbach, EE ;
Schwabe, C .
REPRODUCTION, 2001, 122 (06) :899-906
[3]   Decreased anogenital distance and increased incidence of undescended testes in fetuses of rats given monobenzyl phthalate, a major metabolite of butyl benzyl phthalate [J].
Ema, M ;
Miyawaki, E ;
Hirose, A ;
Kamata, E .
REPRODUCTIVE TOXICOLOGY, 2003, 17 (04) :407-412
[4]   Perinatal exposure to the phthalates DEHP, BBP, and DINP, but not DEP, DMP, or DOTP, alters sexual differentiation of the male rat [J].
Gray, LE ;
Ostby, J ;
Furr, J ;
Price, M ;
Veeramachaneni, DNR ;
Parks, L .
TOXICOLOGICAL SCIENCES, 2000, 58 (02) :350-365
[5]  
HUTSON JM, 1985, LANCET, V2, P419
[6]   Anatomical and functional aspects of testicular descent and cryptorchidism [J].
Hutson, JM ;
Hasthorpe, S ;
Heyns, CF .
ENDOCRINE REVIEWS, 1997, 18 (02) :259-280
[7]   Prenatal phthalate causes cryptorchidism postnatally by inducing transabdominal ascent of the testis in fetal rats [J].
Imajima, T ;
Shono, T ;
Zakaria, O ;
Suita, S .
JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (01) :18-21
[8]   Leydig insulin-like hormone, gubebnacular development and testicular descent [J].
Kubota, Y ;
Nef, S ;
Farmer, PJ ;
Temelcos, C ;
Parada, LF ;
Hutson, JM .
JOURNAL OF UROLOGY, 2001, 165 (05) :1673-1675
[9]   PHTHALATE ESTERS AS ENVIRONMENTAL CONTAMINANTS [J].
MAYER, FL ;
STALLING, DL ;
JOHNSON, JL .
NATURE, 1972, 238 (5364) :411-&
[10]   Disruption of androgen-regulated male reproductive development by Di(n-butyl) phthalate during late gestation in rats is different from flutamide [J].
Mylchreest, E ;
Sar, M ;
Cattley, RC ;
Foster, PMD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1999, 156 (02) :81-95