Masculinization of female mosquitofish in kraft mill effluent-contaminated Fenholloway River water is associated with androgen receptor agonist activity

被引:212
作者
Parks, LG
Lambright, CS
Orlando, EF
Guillette, LJ
Ankley, GT
Gray, LE
机构
[1] US EPA, NHEERL, RTD, Endocrinol Branch, Res Triangle Pk, NC 27711 USA
[2] Univ Florida, Dept Zool, Gainesville, FL 32611 USA
[3] St Marys Coll Maryland, St Marys City, MD USA
[4] US EPA, NHEERL, Mid Continent Ecol Div, Duluth, MN USA
关键词
environmental androgens; Kraft pulp and paper mill effluent; masculinized female mosquitofish anal fin; gonopodium; androgen receptor; glucocorticoid receptor; AR binding; AR gene expression; in vitro; Fenholloway River; Florida;
D O I
10.1093/toxsci/62.2.257
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Female mosquitofish (Gambusia affinis holbrooki) downstream from Kraft paper mills in Florida display masculinization of the anal fin, an androgen-de pendent trait. The current investigation was designed to determine if water contaminated with pulp-mill effluent (PME) from the Fenholloway River in Florida displayed androgenic activity in vitro and to relate this activity to the reproductive status of female mosquitofish taken from this river. We tested water samples for androgenic activity from a reference site upstream of a Kraft pulp and paper mill on the Fenholloway River, from 3 sites downstream from the mill, and from another reference site on the Econfina. River, also in Florida, where there is no paper mill. We also examined anal fin ray morphology in mosquitofish from these rivers for evidence of masculinization. Eighty percent of the female mosquitofish from the Fenholloway River were partially masculinized while another 10% were completely masculinized, based upon the numbers of segments in the longest anal fin ray (18.0 +/- 0.4 vs. 28.1 +/- 0.9 [p < 0.001]) in the Econfina River vs. the Fenholloway River, respectively). In a COS whole cell-binding assay, all 3 PME samples displayed affinity for human androgen receptor (hAR) (p < 0.001). In addition, PME induced androgen-dependent gene expression in CV-1 cells (cotransfected with pCMV hAR and MMTV luciferase reporter), which was inhibited by about 50% by coadministration of hydroxyflutamide (1 muM), an AR antagonist. Water samples collected upstream of the Kraft mill or from the Econfina River did not bind hAR or induce luciferase expression. When CV-1 cells were transfected with human glucocorticoid receptor (hGR) rather than hAR, PME failed to significantly induce MMTV-luciferase expression. Further evidence of the androgenicity was observed using a COS cell AR nuclear-translocalization assay. PME bound hAR and induced translocalization of AR into the nucleus. In contrast, AR remained perinuclear when treated with water from the control sites (indicating the absence of an AR ligand). Interestingly, PME also displayed "testosterone-like" immunoreactivity in a testosterone radioimmunoassay, whereas water from the reference sites did not. In summary, water collected downstream of the Kraft mill on the Fenholloway River contains unidentified androgenic substances whose presence is associated with masculinization of female mosquitofish.
引用
收藏
页码:257 / 267
页数:11
相关论文
共 51 条
[31]  
Norris D. O., 1996, VERTEBRATE ENDOCRINO
[32]  
ORLANDO EF, 2001, AROMATASE ACTIVITY O
[33]  
Raloff Janet, 2001, SCI NEWS, V159, P8
[34]  
RODRIGUEZSIERRA JF, 1990, HORMONES BRAIN BEHAV, V8, P64
[35]  
SCHANBACHER BD, 1975, ENDOCRINOLOGY, V97, P787, DOI 10.1210/endo-97-4-787
[36]  
SCHARDEIN JL, 2000, CHEM INDUCED BIRTH D, P281
[37]   Assessing environmental chemicals for estrogenicity using a combination of in vitro and in vivo assays [J].
Shelby, MD ;
Newbold, RR ;
Tully, DB ;
Chae, K ;
Davis, VL .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1996, 104 (12) :1296-1300
[38]   An updated review of environmental estrogen and androgen mimics and antagonists [J].
Sonnenschein, C ;
Soto, AM .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1998, 65 (1-6) :143-150
[39]   Androgen receptor antagonism by the organophosphate insecticide fenitrothion [J].
Tamura, H ;
Maness, SC ;
Reischmann, K ;
Dorman, DC ;
Gray, LE ;
Gaido, KW .
TOXICOLOGICAL SCIENCES, 2001, 60 (01) :56-62
[40]  
Tremblay L, 1999, ENVIRON TOXICOL CHEM, V18, P329, DOI [10.1002/etc.5620180233, 10.1897/1551-5028(1999)018&lt