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1.
ALTEX ; 31(1): 63-78, 2014.
Article in English | MEDLINE | ID: mdl-24114257

ABSTRACT

In 1996, the U.S. Congress passed the Food Quality Protection Act and amended the Safe Drinking Water Act (SDWA) requiring the U.S. Environmental Protection Agency (EPA) to implement a screening program to investigate the potential of pesticide chemicals and drinking water contaminants to adversely affect endocrine pathways. Consequently, the EPA launched the Endocrine Disruptor Screening Program (EDSP) to develop and validate estrogen, androgen, and thyroid (EAT) pathway screening assays and to produce standardized and harmonized test guidelines for regulatory application. In 2009, the EPA issued the first set of test orders for EDSP screening and a total of 50 pesticide actives and 2 inert ingredients have been evaluated using the battery of EDSP Tier 1 screening assays (i.e., five in vitro assays and six in vivo assays). To provide a framework for retrospective analysis of the data generated and to collect the insight of multiple stakeholders involved in the testing, more than 240 scientists from government, industry, academia, and non-profit organizations recently participated in a workshop titled "Lessons Learned, Challenges, and Opportunities: The U.S. Endocrine Disruptor Screening Program." The workshop focused on the science and experience to date and was organized into three focal sessions: (a) Performance of the EDSP Tier 1 Screening Assays for Estrogen, Androgen, and Thyroid Pathways; (b) Practical Applications of Tier 1 Data; and (c) Indications and Opportunities for Future Endocrine Testing. A number of key learnings and recommendations related to future EDSP evaluations emanated from the collective sessions.


Subject(s)
Animal Testing Alternatives , Endocrine Disruptors/toxicity , Animals , Drug Evaluation, Preclinical , Environmental Pollutants , Toxicity Tests/methods , Toxicity Tests/standards , United States , United States Environmental Protection Agency
2.
Article in English | MEDLINE | ID: mdl-24151143

ABSTRACT

The U.S. Environmental Protection Agency (EPA) Endocrine Disruptor Screening Program (EDSP) currently relies on an initial screening battery (Tier 1) consisting of five in vitro and six in vivo assays to evaluate a chemical's potential to interact with the endocrine system. Chemical companies may request test waivers based on Other Scientifically Relevant Information (OSRI) that is functionally equivalent to data gathered in the screening battery or that provides information on a potential endocrine effect. Respondents for 47 of the first 67 chemicals evaluated in the EDSP submitted OSRI in lieu of some or all Tier 1 tests, seeking 412 waivers, of which EPA granted only 93. For 20 of the 47 chemicals, EPA denied all OSRI and required the entire Tier 1 battery. Often, the OSRI accepted was either identical to data generated by the Tier 1 assay or indicated a positive result. Although identified as potential sources of OSRI in EPA guidance, Part 158 guideline studies for pesticide registration were seldom accepted by EPA. The 93 waivers reduced animal use by at least 3325 animals. We estimate 27,731 animals were used in the actual Tier 1 tests, with additional animals being used in preparation for testing. Even with EPA's shift toward applying 21st-century toxicology tools to screening of endocrine disruptors in the future, acceptance of OSRI will remain a primary means for avoiding duplicative testing and reducing use of animals in the EDSP. Therefore, it is essential that EPA develop a consistent and transparent basis for accepting OSRI.


Subject(s)
Endocrine Disruptors/analysis , Endocrine Disruptors/toxicity , Toxicity Tests/methods , United States Environmental Protection Agency , Animals , Biological Assay , Endpoint Determination , Female , Male , Rats , United States
3.
Environ Health Perspect ; 120(12): 1631-9, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23033452

ABSTRACT

BACKGROUND: Launched by the U.S. Environmental Protection Agency (EPA) in 1998, the High Production Volume (HPV) Challenge Program was developed to address the perceived gap in basic hazard information for the 2,800 chemicals produced or imported into the United States in quantities of ≥ 1 million pounds per year. Health and environmental effects data obtained from either existing information or through new vertebrate animal testing were voluntarily submitted by chemical companies (sponsors) to the U.S. EPA. Despite the potential for extensive animal testing, animal welfare guidelines were not provided until after the start of the program. OBJECTIVES: We evaluated compliance with the animal welfare principles that arose from an agreement reached between the U.S. EPA and animal protection organizations and tracked the HPV program's use of animals for testing. DISCUSSION: Under a worst-case scenario, the HPV program had the potential to consume 3.5 million animals in new testing. After application of animal-saving measures, approximately 127,000 were actually used. Categorization of chemicals based on similar structure-activity and application of read-across, along with use of existing test data, were the most effective means of reducing animal testing. However, animal-saving measures were inconsistently used by both sponsors and the U.S. EPA. CONCLUSIONS: Lessons learned from the HPV program can be applied to future programs to minimize animal testing and promote more human-relevant chemical risk assessment.


Subject(s)
Animal Welfare/standards , Environmental Pollutants/toxicity , Toxicity Tests/standards , Animal Testing Alternatives , Animals , Environmental Pollutants/chemistry , Humans , Risk Assessment , United States , United States Environmental Protection Agency/legislation & jurisprudence
4.
Toxicol Sci ; 123(1): 15-25, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21642633

ABSTRACT

New approaches to generating and evaluating toxicity data for chemicals are needed to cope with the ever-increasing demands of new programs. One such approach involves the use of an integrated testing and evaluation strategy based on the specific properties and activities of a chemical. Such an integrated strategy, whether applied to existing or future programs, can promote efficient use of resources and save animals. We demonstrate the utility of such a strategy by applying it to the current U.S. Environmental Protection Agency Endocrine Disruptor Screening Program (EDSP). Launched in October 2009, the EDSP utilizes a two-tiered approach, whereby each tier requires a battery of animal-intensive and expensive tests. Tier 1 consists of five in vitro and six in vivo assays that are intended to determine a chemical's potential to interact with the estrogen (E), androgen (A), or thyroid (T) hormone pathways. Tier 2 is proposed to consist of multigenerational reproductive and developmental toxicity tests in several species and is intended to determine whether a chemical can cause adverse effects resulting from E, A, or T modulation. In contrast to the existing EDSP structure, we show, using the pesticide atrazine as an example, that a multilevel testing framework combined with an integrated evaluation process would significantly increase efficiency by minimizing testing.


Subject(s)
Endocrine Disruptors/toxicity , Endocrine System/drug effects , Environmental Monitoring/methods , Toxicity Tests/methods , United States Environmental Protection Agency , Xenobiotics/toxicity , Animal Use Alternatives , Animals , Environmental Monitoring/economics , Environmental Monitoring/standards , Female , Male , Program Evaluation , Rats , Toxicity Tests/economics , Toxicity Tests/standards , United States
5.
Brain Res Dev Brain Res ; 153(1): 115-9, 2004 Oct 15.
Article in English | MEDLINE | ID: mdl-15464224

ABSTRACT

The winged-helix/forkhead transcription factor gene, foxn4, is expressed in the nervous system of developing and adult zebrafish. Prominent expression sites include the olfactory placode, the basal layer of the olfactory epithelium, the neuroepithelium of the developing retina, the germinal zone of the differentiated eye, regions of motoneuron development in the neural tube and periventricular regions of the brain. The adult thymus is the only major site of foxn4 expression outside of the nervous system.


Subject(s)
Brain/embryology , Eye Proteins/biosynthesis , Transcription Factors/biosynthesis , Zebrafish Proteins/genetics , Zebrafish/embryology , Amino Acid Sequence , Animals , Eye Proteins/genetics , Gene Expression Regulation, Developmental , In Situ Hybridization , Molecular Sequence Data , Retina/embryology , Skin/embryology , Thymus Gland/embryology , Transcription Factors/genetics , Zebrafish/genetics
6.
Dev Comp Immunol ; 28(7-8): 755-67, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15043944

ABSTRACT

The expression of genes encoding T cell receptor (TCR) alpha was used to follow the development of the thymus and to analyze the distribution of T cells in zebrafish. In the thymus, expression was first detected, by in situ hybridization, at four days post fertilization. In RNA extracted from whole fish, TCRalpha transcripts were also detected at four days and reached adult levels at three weeks. At six weeks, TCRalpha was expressed throughout the thymus, whereas rag1 expression was localized to the peripheral regions. Expression of TCRalpha outside the thymus was detected at nine days. In adult peripheral organs, the greatest expression was in the pronephros, mesonephros and intestine; expression in the spleen became greater as fish age. Three new, relatively highly expressed, TCR Valpha families were identified.


Subject(s)
Intestinal Mucosa/metabolism , Spleen/metabolism , T-Lymphocytes/metabolism , Thymus Gland/metabolism , Zebrafish/metabolism , Amino Acid Sequence , Animals , Embryo, Nonmammalian/metabolism , Gene Expression Regulation, Developmental/genetics , Homeodomain Proteins/metabolism , In Situ Hybridization , Intestines/embryology , Molecular Sequence Data , Receptors, Antigen, T-Cell/metabolism , Spleen/embryology , Thymus Gland/embryology , Zebrafish/embryology , Zebrafish/genetics
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