Effects of tris(1,3-dichloro-2-propyl) phosphate and triphenyl phosphate on receptor-associated mRNA expression in zebrafish embryos/larvae
Creators
- 1. State Key Laboratory of Pollution Control and Resource Reuse and School of the Environment, Nanjing University, Nanjing (China)
- 2. State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072 (China)
- 3. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Beijing 100085 (China)
- 4. Department of Biology and Chemistry, City University of Hong Kong, Kowloon, Hong Kong (China)
- 5. Zoology Department, Center for Integrative Toxicology, Michigan State University, East Lansing, MI 48824 (United States)
- 6. Department of Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5B3 (Canada)
- 7. Toxicology Centre, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5B3 (Canada)
Description
Highlights: ► TDCPP or TPP exposure caused developmental toxicity. ► Receptor-centered PCR array was developed. ► TDCPP or TPP exposure altered mRNA expression in receptor-centered network. -- Abstract: Tris(1,3-dichloro-2-propyl) phosphate (TDCPP) and triphenyl phosphate (TPP) are frequently detected in biota, including fish. However, knowledge of the toxicological and molecular effects of these currently used flame retardants is limited. In the present study, an in vivo screening approach was developed to evaluate effects of TDCPP and TPP on developmental endpoints and receptor-associated expression of mRNA in zebrafish embryos/larvae. Exposure to TDCPP or TPP resulted in significantly smaller rates of hatching and survival, in dose- and time-dependent manners. The median lethal concentration (LC50) was 7.0 mg/L for TDCPP and 29.6 mg/L for TPP at 120 hour post-fertilization (hpf). Real-time PCR revealed alterations in expression of mRNAs involved in aryl hydrocarbon receptors (AhRs)-, peroxisome proliferator-activated receptor alpha (PPARα)-, estrogenic receptors (ERs)-, thyroid hormone receptor alpha (TRα)-, glucocorticoid receptor (GR)-, and mineralocorticoid receptor (MR)-centered gene networks. Exposure to positive control chemicals significantly altered abundances of mRNA in corresponding receptor-centered gene networks, a result that suggests that it is feasible to use zebrafish embryos/larvae to evaluate effects of chemicals on mRNA expression in these gene networks. Exposure to TDCPP altered transcriptional profiles in all six receptor-centered gene networks, thus exerting multiple toxic effects. TPP was easily metabolized and its potency to change expression of mRNA involved in receptor-centered gene networks was weaker than that of TDCPP. The PPARα- and TRα-centered gene networks might be the primary pathways affected by TPP. Taken together, these results demonstrated that TDCPP and TPP could alter mRNA expression of genes involved in the six receptor-centered gene networks in zebrafish embryos/larvae, and TDCPP seemed to have higher potency in changing the mRNA expression of these genes
Availability note (English)
Available from http://dx.doi.org/10.1016/j.aquatox.2012.12.010Additional details
Identifiers
- DOI
- 10.1016/j.aquatox.2012.12.010;
- PII
- S0166-445X(12)00329-3;
Publishing Information
- Journal Title
- Aquatic Toxicology
- Journal Volume
- 128-129
- Journal Page Range
- p. 147-157
- ISSN
- 0166-445X
- CODEN
- AQTODG
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45050713
- Subject category
- S60: APPLIED LIFE SCIENCES; S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- CONCENTRATION RATIO; ECOLOGICAL CONCENTRATION; EMBRYOS; GENES; GLUCOCORTICOIDS; HYDROCARBONS; IN VIVO; LARVAE; MESSENGER-RNA; PHOSPHATES; POLYMERASE CHAIN REACTION; RECEPTORS; THYROID HORMONES; TIME DEPENDENCE; TOXICITY
- Descriptors DEC
- ADRENAL HORMONES; CORTICOSTEROIDS; DIMENSIONLESS NUMBERS; GENE AMPLIFICATION; HORMONES; HYDROXY COMPOUNDS; KETONES; MEMBRANE PROTEINS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PEPTIDE HORMONES; PHOSPHORUS COMPOUNDS; PREGNANES; PROTEINS; RNA; STEROID HORMONES; STEROIDS
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.