Current developments in reproductive toxicity testing of pesticides
A protocol to evaluate the potential developmental and reproductive effects of test chemicals has been developed by the Life Stages Task Force of the International Life Sciences Institute (ILSI)/Health and Environmental Sciences Institute (HESI) Agricultural Chemical Safety Assessment (ACSA) Technic...
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Veröffentlicht in: | Reproductive toxicology (Elmsford, N.Y.) N.Y.), 2009-09, Vol.28 (2), p.180-187 |
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description | A protocol to evaluate the potential developmental and reproductive effects of test chemicals has been developed by the Life Stages Task Force of the International Life Sciences Institute (ILSI)/Health and Environmental Sciences Institute (HESI) Agricultural Chemical Safety Assessment (ACSA) Technical Committee. Since the original publication, several international groups have provided public comment on conducting the test. The extended one-generation reproductive toxicity test is now under consideration as a potential test guideline. The protocol uses a flexible approach that is markedly different from the current multigenerational guidelines. It encourages the use of toxicokinetics when setting the doses, evaluates more than one rat per sex per litter in the F1 offspring and does not necessarily require mating of the F1 to produce an F2 (F1 mating may be triggered by the presence of effects in the P0 and developing F1 rats). A number of additional reproductive endpoints, and the neurotoxicity and immunotoxicity cohorts are included. The ACSA protocol was developed with the goal of assuring that the methods are scientifically appropriate and the toxicological endpoints and exposure durations are relevant for risk assessment. Compared to existing testing strategies, the proposed approach uses substantially fewer animals, provides additional information on the neonate, juvenile and pubertal animal, and includes an estimation of human exposure potential for making decisions about the extent of testing required. In this paper, the evolution of the protocol since the 2006 publication is discussed. These changes reflect the collective input of a U.S. expert panel of government and industrial scientist convened in 2007 and discussions of an OECD expert group held in Paris, France (October, 2008). |
doi_str_mv | 10.1016/j.reprotox.2009.04.014 |
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Since the original publication, several international groups have provided public comment on conducting the test. The extended one-generation reproductive toxicity test is now under consideration as a potential test guideline. The protocol uses a flexible approach that is markedly different from the current multigenerational guidelines. It encourages the use of toxicokinetics when setting the doses, evaluates more than one rat per sex per litter in the F1 offspring and does not necessarily require mating of the F1 to produce an F2 (F1 mating may be triggered by the presence of effects in the P0 and developing F1 rats). A number of additional reproductive endpoints, and the neurotoxicity and immunotoxicity cohorts are included. The ACSA protocol was developed with the goal of assuring that the methods are scientifically appropriate and the toxicological endpoints and exposure durations are relevant for risk assessment. Compared to existing testing strategies, the proposed approach uses substantially fewer animals, provides additional information on the neonate, juvenile and pubertal animal, and includes an estimation of human exposure potential for making decisions about the extent of testing required. In this paper, the evolution of the protocol since the 2006 publication is discussed. These changes reflect the collective input of a U.S. expert panel of government and industrial scientist convened in 2007 and discussions of an OECD expert group held in Paris, France (October, 2008).</description><identifier>ISSN: 0890-6238</identifier><identifier>EISSN: 1873-1708</identifier><identifier>DOI: 10.1016/j.reprotox.2009.04.014</identifier><identifier>PMID: 19409482</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Consensus Development Conferences as Topic ; Embryology: invertebrates and vertebrates. Teratology ; Endpoint Determination - methods ; Female ; Fundamental and applied biological sciences. Psychology ; Guidelines as Topic ; Immune System - drug effects ; Immune System - embryology ; Immune System - growth & development ; Immunotoxicology ; Male ; Medical sciences ; Multigenerational testing ; Nervous System - drug effects ; Nervous System - embryology ; Nervous System - growth & development ; Neurotoxicology ; Pesticides - pharmacokinetics ; Pesticides - toxicity ; Pesticides, fertilizers and other agrochemicals toxicology ; Rats ; Reproduction - drug effects ; Reproduction - physiology ; Reproductive toxicology ; Risk Assessment ; Teratology. 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Since the original publication, several international groups have provided public comment on conducting the test. The extended one-generation reproductive toxicity test is now under consideration as a potential test guideline. The protocol uses a flexible approach that is markedly different from the current multigenerational guidelines. It encourages the use of toxicokinetics when setting the doses, evaluates more than one rat per sex per litter in the F1 offspring and does not necessarily require mating of the F1 to produce an F2 (F1 mating may be triggered by the presence of effects in the P0 and developing F1 rats). A number of additional reproductive endpoints, and the neurotoxicity and immunotoxicity cohorts are included. The ACSA protocol was developed with the goal of assuring that the methods are scientifically appropriate and the toxicological endpoints and exposure durations are relevant for risk assessment. Compared to existing testing strategies, the proposed approach uses substantially fewer animals, provides additional information on the neonate, juvenile and pubertal animal, and includes an estimation of human exposure potential for making decisions about the extent of testing required. In this paper, the evolution of the protocol since the 2006 publication is discussed. These changes reflect the collective input of a U.S. expert panel of government and industrial scientist convened in 2007 and discussions of an OECD expert group held in Paris, France (October, 2008).</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Consensus Development Conferences as Topic</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Endpoint Determination - methods</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guidelines as Topic</subject><subject>Immune System - drug effects</subject><subject>Immune System - embryology</subject><subject>Immune System - growth & development</subject><subject>Immunotoxicology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Multigenerational testing</subject><subject>Nervous System - drug effects</subject><subject>Nervous System - embryology</subject><subject>Nervous System - growth & development</subject><subject>Neurotoxicology</subject><subject>Pesticides - pharmacokinetics</subject><subject>Pesticides - toxicity</subject><subject>Pesticides, fertilizers and other agrochemicals toxicology</subject><subject>Rats</subject><subject>Reproduction - drug effects</subject><subject>Reproduction - physiology</subject><subject>Reproductive toxicology</subject><subject>Risk Assessment</subject><subject>Teratology. 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Teratology</topic><topic>Endpoint Determination - methods</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Guidelines as Topic</topic><topic>Immune System - drug effects</topic><topic>Immune System - embryology</topic><topic>Immune System - growth & development</topic><topic>Immunotoxicology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Multigenerational testing</topic><topic>Nervous System - drug effects</topic><topic>Nervous System - embryology</topic><topic>Nervous System - growth & development</topic><topic>Neurotoxicology</topic><topic>Pesticides - pharmacokinetics</topic><topic>Pesticides - toxicity</topic><topic>Pesticides, fertilizers and other agrochemicals toxicology</topic><topic>Rats</topic><topic>Reproduction - drug effects</topic><topic>Reproduction - physiology</topic><topic>Reproductive toxicology</topic><topic>Risk Assessment</topic><topic>Teratology. Teratogens</topic><topic>Toxicity Tests - methods</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cooper, Ralph L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Reproductive toxicology (Elmsford, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cooper, Ralph L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current developments in reproductive toxicity testing of pesticides</atitle><jtitle>Reproductive toxicology (Elmsford, N.Y.)</jtitle><addtitle>Reprod Toxicol</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>28</volume><issue>2</issue><spage>180</spage><epage>187</epage><pages>180-187</pages><issn>0890-6238</issn><eissn>1873-1708</eissn><abstract>A protocol to evaluate the potential developmental and reproductive effects of test chemicals has been developed by the Life Stages Task Force of the International Life Sciences Institute (ILSI)/Health and Environmental Sciences Institute (HESI) Agricultural Chemical Safety Assessment (ACSA) Technical Committee. Since the original publication, several international groups have provided public comment on conducting the test. The extended one-generation reproductive toxicity test is now under consideration as a potential test guideline. The protocol uses a flexible approach that is markedly different from the current multigenerational guidelines. It encourages the use of toxicokinetics when setting the doses, evaluates more than one rat per sex per litter in the F1 offspring and does not necessarily require mating of the F1 to produce an F2 (F1 mating may be triggered by the presence of effects in the P0 and developing F1 rats). A number of additional reproductive endpoints, and the neurotoxicity and immunotoxicity cohorts are included. The ACSA protocol was developed with the goal of assuring that the methods are scientifically appropriate and the toxicological endpoints and exposure durations are relevant for risk assessment. Compared to existing testing strategies, the proposed approach uses substantially fewer animals, provides additional information on the neonate, juvenile and pubertal animal, and includes an estimation of human exposure potential for making decisions about the extent of testing required. In this paper, the evolution of the protocol since the 2006 publication is discussed. These changes reflect the collective input of a U.S. expert panel of government and industrial scientist convened in 2007 and discussions of an OECD expert group held in Paris, France (October, 2008).</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>19409482</pmid><doi>10.1016/j.reprotox.2009.04.014</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Consensus Development Conferences as Topic Embryology: invertebrates and vertebrates. Teratology Endpoint Determination - methods Female Fundamental and applied biological sciences. Psychology Guidelines as Topic Immune System - drug effects Immune System - embryology Immune System - growth & development Immunotoxicology Male Medical sciences Multigenerational testing Nervous System - drug effects Nervous System - embryology Nervous System - growth & development Neurotoxicology Pesticides - pharmacokinetics Pesticides - toxicity Pesticides, fertilizers and other agrochemicals toxicology Rats Reproduction - drug effects Reproduction - physiology Reproductive toxicology Risk Assessment Teratology. Teratogens Toxicity Tests - methods Toxicology |
title | Current developments in reproductive toxicity testing of pesticides |
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