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An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays
BACKGROUND: For nearly five decades long-term studies in rodents have been the accepted benchmark for assessing chronic long-term toxic effects, particularly carcinogenicity, of chemicals. The European Food Safety Authority (EFSA) and the World Health Organization (WHO) have pointed out that the cur...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Institute of Environmental Health Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332192/ https://www.ncbi.nlm.nih.gov/pubmed/27448388 http://dx.doi.org/10.1289/EHP419 |
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author | Manservisi, Fabiana Marquillas, Clara Babot Buscaroli, Annalisa Huff, James Lauriola, Michelina Mandrioli, Daniele Manservigi, Marco Panzacchi, Simona Silbergeld, Ellen K. Belpoggi, Fiorella |
author_facet | Manservisi, Fabiana Marquillas, Clara Babot Buscaroli, Annalisa Huff, James Lauriola, Michelina Mandrioli, Daniele Manservigi, Marco Panzacchi, Simona Silbergeld, Ellen K. Belpoggi, Fiorella |
author_sort | Manservisi, Fabiana |
collection | PubMed |
description | BACKGROUND: For nearly five decades long-term studies in rodents have been the accepted benchmark for assessing chronic long-term toxic effects, particularly carcinogenicity, of chemicals. The European Food Safety Authority (EFSA) and the World Health Organization (WHO) have pointed out that the current set of internationally utilized test methods capture only some of the potential adverse effects associated with exposures to these agents over the lifetime. OBJECTIVES: In this paper, we propose the adaption of the carcinogenicity bioassay to integrate additional protocols for comprehensive long-term toxicity assessment that includes developmental exposures and long-term outcomes, capable of generating information on a broad spectrum of different end points. DISCUSSION: An integrated study design based on a stepwise process is described that includes the priority end points of the Economic Co-operation and Development and the National Toxicology Program guidelines on carcinogenicity and chronic toxicity and developmental and reproductive toxicity. Integrating a comprehensive set of relevant toxicological end points in a single protocol represents an opportunity to optimize animal use in accordance with the 3Rs (replacement, reduction and refinement). This strategy has the potential to provide sufficient data on multiple windows of susceptibility of specific interest for risk assessments and public health decision-making by including prenatal, lactational, neonatal exposures and evaluating outcomes over the lifespan. CONCLUSION: This integrated study design is efficient in that the same generational cohort of rats used for evaluating long-term outcomes can be monitored in satellite parallel experiments to measure biomarkers and other parameters related to system-specific responses including metabolic alterations and endocrine disturbances. CITATION: Manservisi F, Babot Marquillas C, Buscaroli A, Huff J, Lauriola M, Mandrioli D, Manservigi M, Panzacchi S, Silbergeld EK, Belpoggi F. 2017. An integrated experimental design for the assessment of multiple toxicological end points in rat bioassays. Environ Health Perspect 125:289–295; http://dx.doi.org/10.1289/EHP419 |
format | Online Article Text |
id | pubmed-5332192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | National Institute of Environmental Health Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-53321922017-03-15 An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays Manservisi, Fabiana Marquillas, Clara Babot Buscaroli, Annalisa Huff, James Lauriola, Michelina Mandrioli, Daniele Manservigi, Marco Panzacchi, Simona Silbergeld, Ellen K. Belpoggi, Fiorella Environ Health Perspect Commentary BACKGROUND: For nearly five decades long-term studies in rodents have been the accepted benchmark for assessing chronic long-term toxic effects, particularly carcinogenicity, of chemicals. The European Food Safety Authority (EFSA) and the World Health Organization (WHO) have pointed out that the current set of internationally utilized test methods capture only some of the potential adverse effects associated with exposures to these agents over the lifetime. OBJECTIVES: In this paper, we propose the adaption of the carcinogenicity bioassay to integrate additional protocols for comprehensive long-term toxicity assessment that includes developmental exposures and long-term outcomes, capable of generating information on a broad spectrum of different end points. DISCUSSION: An integrated study design based on a stepwise process is described that includes the priority end points of the Economic Co-operation and Development and the National Toxicology Program guidelines on carcinogenicity and chronic toxicity and developmental and reproductive toxicity. Integrating a comprehensive set of relevant toxicological end points in a single protocol represents an opportunity to optimize animal use in accordance with the 3Rs (replacement, reduction and refinement). This strategy has the potential to provide sufficient data on multiple windows of susceptibility of specific interest for risk assessments and public health decision-making by including prenatal, lactational, neonatal exposures and evaluating outcomes over the lifespan. CONCLUSION: This integrated study design is efficient in that the same generational cohort of rats used for evaluating long-term outcomes can be monitored in satellite parallel experiments to measure biomarkers and other parameters related to system-specific responses including metabolic alterations and endocrine disturbances. CITATION: Manservisi F, Babot Marquillas C, Buscaroli A, Huff J, Lauriola M, Mandrioli D, Manservigi M, Panzacchi S, Silbergeld EK, Belpoggi F. 2017. An integrated experimental design for the assessment of multiple toxicological end points in rat bioassays. Environ Health Perspect 125:289–295; http://dx.doi.org/10.1289/EHP419 National Institute of Environmental Health Sciences 2016-07-22 2017-03 /pmc/articles/PMC5332192/ /pubmed/27448388 http://dx.doi.org/10.1289/EHP419 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, “Reproduced with permission from Environmental Health Perspectives”); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright. |
spellingShingle | Commentary Manservisi, Fabiana Marquillas, Clara Babot Buscaroli, Annalisa Huff, James Lauriola, Michelina Mandrioli, Daniele Manservigi, Marco Panzacchi, Simona Silbergeld, Ellen K. Belpoggi, Fiorella An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays |
title | An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays |
title_full | An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays |
title_fullStr | An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays |
title_full_unstemmed | An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays |
title_short | An Integrated Experimental Design for the Assessment of Multiple Toxicological End Points in Rat Bioassays |
title_sort | integrated experimental design for the assessment of multiple toxicological end points in rat bioassays |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332192/ https://www.ncbi.nlm.nih.gov/pubmed/27448388 http://dx.doi.org/10.1289/EHP419 |
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