Atrazine is an immune disruptor in adult northern leopard frogs (Rana pipiens)

被引:77
作者
Brodkin, Marc A. [1 ]
Madhoun, Hareth [1 ]
Rameswaran, Muthuramanan [1 ]
Vatnick, Itzick [1 ]
机构
[1] Widener Univ, Dept Biol, Div Sci, Chester, PA 19013 USA
关键词
atrazine; immune disruption; frog; Rana pipiens;
D O I
10.1897/05-469.1
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Atrazine, the most widely used herbicide in the United States, has been shown in several studies to be an endocrine disruptor in adult frogs. Results from this study indicate that atrazine also functions as an immune disrupter in frogs. Exposure to atrazine (21 ppb for 8 d) affects the innate immune response of adult Rana pipiens in similar ways to acid exposure (pH 5.5), as we have previously shown. Atrazine exposure suppressed the thioglycollate-stimulated recruitment of white blood cells to the peritoneal cavity to background (Ringer exposed) levels and also decreased the phagocytic activity of these cells. Unlike acid exposure, atrazine exposure did not cause mortality. Our results, from a dose-response study. indicate that atrazine acts as an immune disruptor at the same effective doses that it disrupts the endocrine system.
引用
收藏
页码:80 / 84
页数:5
相关论文
共 24 条
[1]  
Aspelin A, 1994, 733K94001 US EPA
[2]  
ASPELIN AL, 1999, 733R97002 US EPA
[3]  
Chadzinska Magdalena, 1997, Archivum Immunologiae et Therapiae Experimentalis, V45, P321
[4]   Environmental signaling:: A biological context for endocrine disruption [J].
Cheek, AO ;
Vonier, PM ;
Oberdörster, E ;
Burow, BC ;
McLachlan, JA .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1998, 106 :5-10
[5]  
CHISTIN MS, 2003, ENVIRON TOXICOL CHEM, V22, P1127
[6]   Emerging infectious diseases and amphibian population declines [J].
Daszak, P ;
Berger, L ;
Cunningham, AA ;
Hyatt, AD ;
Green, DE ;
Speare, R .
EMERGING INFECTIOUS DISEASES, 1999, 5 (06) :735-748
[7]  
DENOTTER W, 1982, EXP MOL PATHOL, V36, P403
[8]   Morphine-induced enhancement in the granulocyte response to thioglycollate administration in the rat [J].
Fecho, K ;
Lysle, DT .
INFLAMMATION, 2002, 26 (06) :259-271
[9]  
Gilbertson MK, 2003, ENVIRON TOXICOL CHEM, V22, P101, DOI [10.1002/etc.5620220113, 10.1897/1551-5028(2003)022&lt
[10]  
0101:IITNLF&gt