ToxSci Advance Access originally published online on May 18, 2005
Toxicological Sciences 2005 87(2):497-507; doi:10.1093/toxsci/kfi201
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Accumulation, Tissue Distribution, and Maternal Transfer of Dietary 2,3,7,8,-Tetrachlorodibenzo-p-Dioxin: Impacts on Reproductive Success of Zebrafish
* Marine and Freshwater Biomedical Sciences Center, University of Wisconsin-Milwaukee Great Lakes WATER Institute, Milwaukee, Wisconsin 53204, and Department of Biological Sciences, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin 53211
Received February 28, 2005; accepted May 6, 2005
TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin) is a reproductive toxicant and endocrine disruptor in nearly all vertebrates; however, the mechanisms by which TCDD alters the reproductive system is not well understood. The zebrafish provides a powerful vertebrate model system to investigate molecular mechanisms by which TCDD affects the reproductive system, but little is known regarding reproductive toxic response of zebrafish following chronic, sublethal exposure to TCDD. Here we investigate the accumulation of TCDD in selected tissues of adult female zebrafish and maternal transfer to offspring following dietary exposure to TCDD (0.08–2.16 ng TCDD/fish/day). TCDD accumulated in tissues of zebrafish in a dose- and time-dependent manner, except for brain. Chronic dietary exposure resulting in the accumulation of 1.1–36 ng/g fish did not induce an overt toxic response or suppress spawning activity. The ovosomatic index was impacted with an accumulation of as little as 0.6 ng/g fish, and 10% of the females showed signs of ovarian necrosis following accumulation of approximately 3 ng/g TCDD. Offspring health was impacted with an accumulation of as little as 1.1 ng/g female; thus the lowest observed effect level (LOEL) for reproductive toxicity in female zebrafish is approximately 0.6–1.1 ng/g fish. Maternal transfer resulted in the accumulation of 0.094–1.2 ng/g, TCDD, which was sufficient to induce the typical endpoints of larval TCDD toxicity, commonly referred to as blue sac syndrome. This study provides the necessary framework to utilize the zebrafish model system for further investigations into the molecular mechanisms by which TCDD exerts its reproductive toxic responses.
Key Words: TCDD; bioaccumulation; maternal transfer; zebrafish.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  T. C. King Heiden, J. Spitsbergen, W. Heideman, and R. E. Peterson Persistent Adverse Effects on Health and Reproduction Caused by Exposure of Zebrafish to 2,3,7,8-Tetrachlorodibenzo-p-dioxin During Early Development and Gonad Differentiation Toxicol. Sci., May 1, 2009; 109(1): 75 - 87. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. S. Antkiewicz, R. E. Peterson, and W. Heideman Blocking Expression of AHR2 and ARNT1 in Zebrafish Larvae Protects Against Cardiac Toxicity of 2,3,7,8-Tetrachlorodibenzo-p-dioxin Toxicol. Sci., November 1, 2006; 94(1): 175 - 182. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
T. King Heiden, M. J. Carvan III, and R. J. Hutz Inhibition of Follicular Development, Vitellogenesis, and Serum 17{beta}-Estradiol Concentrations in Zebrafish Following Chronic, Sublethal Dietary Exposure to 2,3,7,8-Tetrachlorodibenzo-p-Dioxin Toxicol. Sci., April 1, 2006; 90(2): 490 - 499. [Abstract] [Full Text] [PDF]
|
|