Oral (Gavage) Combined Developmental and Perinatal/Postnatal Reproduction Toxicity Study of Ammonium Salt of Perfluorinated Hexanoic Acid in Mice

The reproductive toxicity potential of Ammonium Salt of Perfluorinated Hexanoic Acid (PFHxA Ammonium Salt) in pregnant Crl: CD1(ICR) mice was investigated. Twenty females/group were administered the test substance or vehicle once daily from gestation day 6 through 18. Phase 1 doses: 0, 100, 350, and...

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Veröffentlicht in:International journal of toxicology 2014-05, Vol.33 (3), p.219-237
Hauptverfasser: Iwai, Hiroyuki, Hoberman, Alan M.
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description The reproductive toxicity potential of Ammonium Salt of Perfluorinated Hexanoic Acid (PFHxA Ammonium Salt) in pregnant Crl: CD1(ICR) mice was investigated. Twenty females/group were administered the test substance or vehicle once daily from gestation day 6 through 18. Phase 1 doses: 0, 100, 350, and 500 mg/kg/d; phase 2: 0, 7, 35, and 175 mg/kg/d. Parameters evaluated include mortality, viability, body weights, clinical signs, abortions, premature deliveries, pregnancy and fertility, litter observations, maternal behavior, and sexual maturity in the F1 generation. The level of PFHxA Ammonium Salt was measured in the liver of F0 and F1 mice. At doses of 350 and 500 mg/kg/d maternal mortalities, excess salivation and changes in body weight gains occurred. Pup body weights were reduced on postpartum day (PPD) 0 in all the dosage groups, but persisted only in the 350 and 500 mg/kg/d groups. Additional effects at 300 and 500 mg/kg/d included stillbirths, reductions in viability indices, and delays in physical development. Levels of PFHxA Ammonium Salt in the livers of the 100 mg/kg/d dams were all below the lower limit of quantization (0.02 µg/mL); in the 350 mg/kg/d group, 3 of the 8 samples had quantifiable analytical results. In phase 2 no PFHxA Ammonium Salt was found in the liver. Adverse effects occurred only in the 175 mg/kg/d group and consisted of increased stillborn pups, pups dying on PPD 1, and reduced pup weights on PPD 1. Based on these data, the maternal and reproductive no observable adverse effect level of PFHxA Ammonium Salt is 100 mg/kg/d.
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Twenty females/group were administered the test substance or vehicle once daily from gestation day 6 through 18. Phase 1 doses: 0, 100, 350, and 500 mg/kg/d; phase 2: 0, 7, 35, and 175 mg/kg/d. Parameters evaluated include mortality, viability, body weights, clinical signs, abortions, premature deliveries, pregnancy and fertility, litter observations, maternal behavior, and sexual maturity in the F1 generation. The level of PFHxA Ammonium Salt was measured in the liver of F0 and F1 mice. At doses of 350 and 500 mg/kg/d maternal mortalities, excess salivation and changes in body weight gains occurred. Pup body weights were reduced on postpartum day (PPD) 0 in all the dosage groups, but persisted only in the 350 and 500 mg/kg/d groups. Additional effects at 300 and 500 mg/kg/d included stillbirths, reductions in viability indices, and delays in physical development. Levels of PFHxA Ammonium Salt in the livers of the 100 mg/kg/d dams were all below the lower limit of quantization (0.02 µg/mL); in the 350 mg/kg/d group, 3 of the 8 samples had quantifiable analytical results. In phase 2 no PFHxA Ammonium Salt was found in the liver. Adverse effects occurred only in the 175 mg/kg/d group and consisted of increased stillborn pups, pups dying on PPD 1, and reduced pup weights on PPD 1. 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Twenty females/group were administered the test substance or vehicle once daily from gestation day 6 through 18. Phase 1 doses: 0, 100, 350, and 500 mg/kg/d; phase 2: 0, 7, 35, and 175 mg/kg/d. Parameters evaluated include mortality, viability, body weights, clinical signs, abortions, premature deliveries, pregnancy and fertility, litter observations, maternal behavior, and sexual maturity in the F1 generation. The level of PFHxA Ammonium Salt was measured in the liver of F0 and F1 mice. At doses of 350 and 500 mg/kg/d maternal mortalities, excess salivation and changes in body weight gains occurred. Pup body weights were reduced on postpartum day (PPD) 0 in all the dosage groups, but persisted only in the 350 and 500 mg/kg/d groups. Additional effects at 300 and 500 mg/kg/d included stillbirths, reductions in viability indices, and delays in physical development. Levels of PFHxA Ammonium Salt in the livers of the 100 mg/kg/d dams were all below the lower limit of quantization (0.02 µg/mL); in the 350 mg/kg/d group, 3 of the 8 samples had quantifiable analytical results. In phase 2 no PFHxA Ammonium Salt was found in the liver. Adverse effects occurred only in the 175 mg/kg/d group and consisted of increased stillborn pups, pups dying on PPD 1, and reduced pup weights on PPD 1. Based on these data, the maternal and reproductive no observable adverse effect level of PFHxA Ammonium Salt is 100 mg/kg/d.</description><subject>Administration, Oral</subject><subject>Ammonium Chloride - administration &amp; dosage</subject><subject>Ammonium Chloride - chemistry</subject><subject>Ammonium Chloride - metabolism</subject><subject>Ammonium Chloride - toxicity</subject><subject>Animals</subject><subject>Caproates - administration &amp; dosage</subject><subject>Caproates - chemistry</subject><subject>Caproates - metabolism</subject><subject>Caproates - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Environmental Pollutants - administration &amp; dosage</subject><subject>Environmental Pollutants - chemistry</subject><subject>Environmental Pollutants - metabolism</subject><subject>Environmental Pollutants - toxicity</subject><subject>Female</subject><subject>Fetal Development - drug effects</subject><subject>Fluorocarbons - administration &amp; dosage</subject><subject>Fluorocarbons - chemistry</subject><subject>Fluorocarbons - metabolism</subject><subject>Fluorocarbons - toxicity</subject><subject>Infertility, Female - chemically induced</subject><subject>Infertility, Female - metabolism</subject><subject>Infertility, Female - pathology</subject><subject>Infertility, Male - chemically induced</subject><subject>Infertility, Male - metabolism</subject><subject>Infertility, Male - pathology</subject><subject>Lactation</subject><subject>Male</subject><subject>Maternal Exposure - adverse effects</subject><subject>Mice</subject><subject>No-Observed-Adverse-Effect Level</subject><subject>Pregnancy</subject><subject>Pregnancy Complications - chemically induced</subject><subject>Pregnancy Complications - metabolism</subject><subject>Pregnancy Complications - pathology</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Sexual Maturation - drug effects</subject><subject>Tissue Distribution</subject><subject>Toxicokinetics</subject><subject>Weight Gain - drug effects</subject><issn>1091-5818</issn><issn>1092-874X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kcFO3DAQhi3UCijlzqnykR5SxnYcO8fV0kIlKlABiVvk2JPKKLG3cYLYx-gb17sLHCr15PHMP9_onyHkhMEXxpQ6Y1AzqZlmpeR1WdZ75DCneKFV-fBuG7NiUz8gH1J6BIBKSbZPDnipAGSlD8mf69H09PTCPJlf-Jku49D6gI6e4xP2cTVgmHLdBEdvcPTB5N_ZTUzTNqI_cTVGN9vJx0Dv4rO3flrT22l2axo7uhiGGPw80FvTT5tEZnT9HLegPOQSn02I3tKF9Y76QH94ix_J-870CY9f3iNy_-3r3fKyuLq--L5cXBVWCDUVGqSpAVmLTjlXMYFWcQDeVk4LI2QneXbOROUEMNAVSgfW8E4LLaFqQRyR0x03W_g9Y5qawSeLfW8Cxjk1TPNK1sC4ylLYSe0YUxqxa1ajH8y4bhg0m0M0_x4it3x6oc_tgO6t4XXzWVDsBCkvvnmM8xiy2_8D_wIYCZDB</recordid><startdate>20140501</startdate><enddate>20140501</enddate><creator>Iwai, Hiroyuki</creator><creator>Hoberman, Alan M.</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140501</creationdate><title>Oral (Gavage) Combined Developmental and Perinatal/Postnatal Reproduction Toxicity Study of Ammonium Salt of Perfluorinated Hexanoic Acid in Mice</title><author>Iwai, Hiroyuki ; Hoberman, Alan M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-805a90e1bed7dd613ec72002b6d83a35f52581136d301086e5d0ca2f838506b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Administration, Oral</topic><topic>Ammonium Chloride - administration &amp; dosage</topic><topic>Ammonium Chloride - chemistry</topic><topic>Ammonium Chloride - metabolism</topic><topic>Ammonium Chloride - toxicity</topic><topic>Animals</topic><topic>Caproates - administration &amp; dosage</topic><topic>Caproates - chemistry</topic><topic>Caproates - metabolism</topic><topic>Caproates - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Environmental Pollutants - administration &amp; dosage</topic><topic>Environmental Pollutants - chemistry</topic><topic>Environmental Pollutants - metabolism</topic><topic>Environmental Pollutants - toxicity</topic><topic>Female</topic><topic>Fetal Development - drug effects</topic><topic>Fluorocarbons - administration &amp; dosage</topic><topic>Fluorocarbons - chemistry</topic><topic>Fluorocarbons - metabolism</topic><topic>Fluorocarbons - toxicity</topic><topic>Infertility, Female - chemically induced</topic><topic>Infertility, Female - metabolism</topic><topic>Infertility, Female - pathology</topic><topic>Infertility, Male - chemically induced</topic><topic>Infertility, Male - metabolism</topic><topic>Infertility, Male - pathology</topic><topic>Lactation</topic><topic>Male</topic><topic>Maternal Exposure - adverse effects</topic><topic>Mice</topic><topic>No-Observed-Adverse-Effect Level</topic><topic>Pregnancy</topic><topic>Pregnancy Complications - chemically induced</topic><topic>Pregnancy Complications - metabolism</topic><topic>Pregnancy Complications - pathology</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Sexual Maturation - drug effects</topic><topic>Tissue Distribution</topic><topic>Toxicokinetics</topic><topic>Weight Gain - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iwai, Hiroyuki</creatorcontrib><creatorcontrib>Hoberman, Alan M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iwai, Hiroyuki</au><au>Hoberman, Alan M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral (Gavage) Combined Developmental and Perinatal/Postnatal Reproduction Toxicity Study of Ammonium Salt of Perfluorinated Hexanoic Acid in Mice</atitle><jtitle>International journal of toxicology</jtitle><addtitle>Int J Toxicol</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>33</volume><issue>3</issue><spage>219</spage><epage>237</epage><pages>219-237</pages><issn>1091-5818</issn><eissn>1092-874X</eissn><abstract>The reproductive toxicity potential of Ammonium Salt of Perfluorinated Hexanoic Acid (PFHxA Ammonium Salt) in pregnant Crl: CD1(ICR) mice was investigated. Twenty females/group were administered the test substance or vehicle once daily from gestation day 6 through 18. Phase 1 doses: 0, 100, 350, and 500 mg/kg/d; phase 2: 0, 7, 35, and 175 mg/kg/d. Parameters evaluated include mortality, viability, body weights, clinical signs, abortions, premature deliveries, pregnancy and fertility, litter observations, maternal behavior, and sexual maturity in the F1 generation. The level of PFHxA Ammonium Salt was measured in the liver of F0 and F1 mice. At doses of 350 and 500 mg/kg/d maternal mortalities, excess salivation and changes in body weight gains occurred. Pup body weights were reduced on postpartum day (PPD) 0 in all the dosage groups, but persisted only in the 350 and 500 mg/kg/d groups. Additional effects at 300 and 500 mg/kg/d included stillbirths, reductions in viability indices, and delays in physical development. Levels of PFHxA Ammonium Salt in the livers of the 100 mg/kg/d dams were all below the lower limit of quantization (0.02 µg/mL); in the 350 mg/kg/d group, 3 of the 8 samples had quantifiable analytical results. In phase 2 no PFHxA Ammonium Salt was found in the liver. Adverse effects occurred only in the 175 mg/kg/d group and consisted of increased stillborn pups, pups dying on PPD 1, and reduced pup weights on PPD 1. Based on these data, the maternal and reproductive no observable adverse effect level of PFHxA Ammonium Salt is 100 mg/kg/d.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>24700568</pmid><doi>10.1177/1091581814529449</doi><tpages>19</tpages></addata></record>
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subjects Administration, Oral
Ammonium Chloride - administration & dosage
Ammonium Chloride - chemistry
Ammonium Chloride - metabolism
Ammonium Chloride - toxicity
Animals
Caproates - administration & dosage
Caproates - chemistry
Caproates - metabolism
Caproates - toxicity
Dose-Response Relationship, Drug
Environmental Pollutants - administration & dosage
Environmental Pollutants - chemistry
Environmental Pollutants - metabolism
Environmental Pollutants - toxicity
Female
Fetal Development - drug effects
Fluorocarbons - administration & dosage
Fluorocarbons - chemistry
Fluorocarbons - metabolism
Fluorocarbons - toxicity
Infertility, Female - chemically induced
Infertility, Female - metabolism
Infertility, Female - pathology
Infertility, Male - chemically induced
Infertility, Male - metabolism
Infertility, Male - pathology
Lactation
Male
Maternal Exposure - adverse effects
Mice
No-Observed-Adverse-Effect Level
Pregnancy
Pregnancy Complications - chemically induced
Pregnancy Complications - metabolism
Pregnancy Complications - pathology
Prenatal Exposure Delayed Effects
Sexual Maturation - drug effects
Tissue Distribution
Toxicokinetics
Weight Gain - drug effects
title Oral (Gavage) Combined Developmental and Perinatal/Postnatal Reproduction Toxicity Study of Ammonium Salt of Perfluorinated Hexanoic Acid in Mice
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