Developing a laboratory animal model for perinatal endocrine disruption: The hamster chronicles

被引:21
作者
Hendry, WJ
Sheehan, DM
Khan, SA
May, JV
机构
[1] Wichita State Univ, Dept Biol Sci, Wichita, KS 67260 USA
[2] Univ Kansas, Sch Med, Womens Res Inst, Wichita, KS 67208 USA
[3] Univ Kansas, Sch Med, Dept Obstet & Gynecol, Wichita, KS 67208 USA
[4] Natl Ctr Toxicol Res, Div Genet & Reprod Toxicol, Jefferson, AR 72079 USA
[5] Texas Tech Univ, Hlth Sci Ctr, Univ Med Ctr, Dept Biochem & Cell Biol, Lubbock, TX 79430 USA
[6] Texas Tech Univ, Hlth Sci Ctr, Univ Med Ctr, SW Canc Ctr, Lubbock, TX 79430 USA
关键词
endocrine disruption; diethylstilbestrol; estrogen; cheek pouch; transplantation;
D O I
10.1177/153537020222700904
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
At the biomedical, regulatory, and public level, considerable concern surrounds the concept that inappropriate exposure to endocrine-disrupting chemicals, especially during the prenatal and/or neonatal period, may disrupt normal reproductive tract development and adult function. The intent of this review was to 1. Describe some unique advantages of the hamster for perinatal endocrine disruptor (ED) studies, 2. Summarize the morphological and molecular consequences of exposure to the established perinatal ED, diethylstilbestrol, in the female and male hamster, 3. Present some new, histomorphological insight into the process of neonatal diethylstilbestrol-Induced disruption in the hamster uterus, and 4. Introduce recent efforts and future plans to evaluate the potency and mechanism of action of other putative EDs in the hamster experimental system. Taken together, the findings Indicate that the hamster represents a unique and sensitive In vivo system to probe the phenomenon of endocrine disruption. The spectrum of candidate endpoints includes developmental toxicity, neoplasia, and more subtle endpoints of reproductive dysfunction.
引用
收藏
页码:709 / 723
页数:15
相关论文
共 127 条
[1]   Getting the problem of endocrine disruption into focus: The need for a pause for thought [J].
Ashby, J .
APMIS, 2000, 108 (12) :805-813
[2]   CELL-DEATH IN HEALTH AND DISEASE - THE BIOLOGY AND REGULATION OF APOPTOSIS [J].
BELLAMY, COC ;
MALCOMSON, RDG ;
HARRISON, DJ ;
WYLLIE, AH .
SEMINARS IN CANCER BIOLOGY, 1995, 6 (01) :3-16
[3]  
Bigsby R, 1999, ENVIRON HEALTH PERSP, V107, P613, DOI 10.2307/3434553
[4]   A SIMPLE EFFICIENT METHOD FOR SEPARATING MURINE UTERINE EPITHELIAL AND MESENCHYMAL CELLS [J].
BIGSBY, RM ;
COOKE, PS ;
CUNHA, GR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (05) :E630-E636
[5]  
Bloch DB, 1999, MOL CELL BIOL, V19, P4423
[6]   NUCLEAR-BODIES (NBS) - A NEWLY REDISCOVERED ORGANELLE [J].
BRASCH, K ;
OCHS, RL .
EXPERIMENTAL CELL RESEARCH, 1992, 202 (02) :211-223
[7]  
BULLETTI C, 1988, CANCER, V62, P142, DOI 10.1002/1097-0142(19880701)62:1<142::AID-CNCR2820620124>3.0.CO
[8]  
2-Y
[9]  
CALDWELL BV, 1966, P SOC EXP BIOL MED, V123, P551, DOI 10.3181/00379727-123-31540
[10]  
CHIANG T, 1991, CARCINOGENESIS, V12, P529