Inhalation teratology studies of n-butyl mercaptan in rats and mice
n-Butyl mercaptan ( n-BM) is used as a solvent and a chemical intermediate. Pregnant Charles River CD-1 mice and COBS CD rats were randomly assigned to a control group and to three n-BM-exposed groups of 25 rats and 25 mice each. The animals were exposed by whole-body inhalation to mean n-BM concent...
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Veröffentlicht in: | Fundamental and applied toxicology 1987-02, Vol.8 (2), p.170-178 |
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creator | Thomas, William C. Seckar, Joel A. Johnson, J.Timothy Ulrich, Charles E. Klonne, Dennis R. Schardein, James L. Kirwin, Carroll J. |
description | n-Butyl mercaptan (
n-BM) is used as a solvent and a chemical intermediate. Pregnant Charles River CD-1 mice and COBS CD rats were randomly assigned to a control group and to three
n-BM-exposed groups of 25 rats and 25 mice each. The animals were exposed by whole-body inhalation to mean
n-BM concentrations of 10, 68, or 152 ppm on a 6-hr daily exposure schedule. Rats were exposed on Gestation Days 6–19 and mice on Gestation Days 6–16. The control group was exposed to filtered air only on a comparable regimen. Cesarean sections were performed on all surviving mice on Gestation Day 17 and on all rats on Gestation Day 20. Seventeen of the
n-BM-treated mice died: 8 at the 68-ppm level and 9 at the 152-ppm level; none of the
n-BM-treated rats died. An increased postimplantation loss and increased early resorption occurred in mice exposed at 68 and 152 ppm, indicating embryotoxicity. An increased incidence of cleft palate was observed in mice exposed to 10 or 68 ppm which was not statistically significant. Total fetal abnormalities were statistically significantly different from controls at 68 ppm where maternal lethality was observed when based on the fetal unit although not when based on the litter unit. Rats exposed to 152 ppm or less demonstrated no terata. |
doi_str_mv | 10.1016/0272-0590(87)90115-1 |
format | Article |
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n-BM) is used as a solvent and a chemical intermediate. Pregnant Charles River CD-1 mice and COBS CD rats were randomly assigned to a control group and to three
n-BM-exposed groups of 25 rats and 25 mice each. The animals were exposed by whole-body inhalation to mean
n-BM concentrations of 10, 68, or 152 ppm on a 6-hr daily exposure schedule. Rats were exposed on Gestation Days 6–19 and mice on Gestation Days 6–16. The control group was exposed to filtered air only on a comparable regimen. Cesarean sections were performed on all surviving mice on Gestation Day 17 and on all rats on Gestation Day 20. Seventeen of the
n-BM-treated mice died: 8 at the 68-ppm level and 9 at the 152-ppm level; none of the
n-BM-treated rats died. An increased postimplantation loss and increased early resorption occurred in mice exposed at 68 and 152 ppm, indicating embryotoxicity. An increased incidence of cleft palate was observed in mice exposed to 10 or 68 ppm which was not statistically significant. Total fetal abnormalities were statistically significantly different from controls at 68 ppm where maternal lethality was observed when based on the fetal unit although not when based on the litter unit. Rats exposed to 152 ppm or less demonstrated no terata.</description><identifier>ISSN: 0272-0590</identifier><identifier>EISSN: 1095-6832</identifier><identifier>DOI: 10.1016/0272-0590(87)90115-1</identifier><identifier>PMID: 3556829</identifier><identifier>CODEN: FAATDF</identifier><language>eng</language><publisher>Boston, MA: Elsevier Science (USA)</publisher><subject>Abnormalities, Drug-Induced - pathology ; Administration, Inhalation ; Animals ; Biological and medical sciences ; Body Weight - drug effects ; Embryology: invertebrates and vertebrates. Teratology ; Female ; Fundamental and applied biological sciences. Psychology ; Mice ; Pregnancy ; Rats ; Rats, Inbred Strains ; Species Specificity ; Sulfhydryl Compounds - administration & dosage ; Sulfhydryl Compounds - toxicity ; Teratogens ; Teratology. Teratogens</subject><ispartof>Fundamental and applied toxicology, 1987-02, Vol.8 (2), p.170-178</ispartof><rights>1987</rights><rights>1987 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2649-fb7a38f0586a072a762e9ec31725f1486159d86df9e83880e2406fc21b6cef193</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8215974$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3556829$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thomas, William C.</creatorcontrib><creatorcontrib>Seckar, Joel A.</creatorcontrib><creatorcontrib>Johnson, J.Timothy</creatorcontrib><creatorcontrib>Ulrich, Charles E.</creatorcontrib><creatorcontrib>Klonne, Dennis R.</creatorcontrib><creatorcontrib>Schardein, James L.</creatorcontrib><creatorcontrib>Kirwin, Carroll J.</creatorcontrib><title>Inhalation teratology studies of n-butyl mercaptan in rats and mice</title><title>Fundamental and applied toxicology</title><addtitle>Fundam Appl Toxicol</addtitle><description>n-Butyl mercaptan (
n-BM) is used as a solvent and a chemical intermediate. Pregnant Charles River CD-1 mice and COBS CD rats were randomly assigned to a control group and to three
n-BM-exposed groups of 25 rats and 25 mice each. The animals were exposed by whole-body inhalation to mean
n-BM concentrations of 10, 68, or 152 ppm on a 6-hr daily exposure schedule. Rats were exposed on Gestation Days 6–19 and mice on Gestation Days 6–16. The control group was exposed to filtered air only on a comparable regimen. Cesarean sections were performed on all surviving mice on Gestation Day 17 and on all rats on Gestation Day 20. Seventeen of the
n-BM-treated mice died: 8 at the 68-ppm level and 9 at the 152-ppm level; none of the
n-BM-treated rats died. An increased postimplantation loss and increased early resorption occurred in mice exposed at 68 and 152 ppm, indicating embryotoxicity. An increased incidence of cleft palate was observed in mice exposed to 10 or 68 ppm which was not statistically significant. Total fetal abnormalities were statistically significantly different from controls at 68 ppm where maternal lethality was observed when based on the fetal unit although not when based on the litter unit. Rats exposed to 152 ppm or less demonstrated no terata.</description><subject>Abnormalities, Drug-Induced - pathology</subject><subject>Administration, Inhalation</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Mice</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Species Specificity</subject><subject>Sulfhydryl Compounds - administration & dosage</subject><subject>Sulfhydryl Compounds - toxicity</subject><subject>Teratogens</subject><subject>Teratology. 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Teratology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Mice</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Species Specificity</topic><topic>Sulfhydryl Compounds - administration & dosage</topic><topic>Sulfhydryl Compounds - toxicity</topic><topic>Teratogens</topic><topic>Teratology. Teratogens</topic><toplevel>online_resources</toplevel><creatorcontrib>Thomas, William C.</creatorcontrib><creatorcontrib>Seckar, Joel A.</creatorcontrib><creatorcontrib>Johnson, J.Timothy</creatorcontrib><creatorcontrib>Ulrich, Charles E.</creatorcontrib><creatorcontrib>Klonne, Dennis R.</creatorcontrib><creatorcontrib>Schardein, James L.</creatorcontrib><creatorcontrib>Kirwin, Carroll J.</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>Health and Safety Science Abstracts (Full archive)</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Fundamental and applied toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomas, William C.</au><au>Seckar, Joel A.</au><au>Johnson, J.Timothy</au><au>Ulrich, Charles E.</au><au>Klonne, Dennis R.</au><au>Schardein, James L.</au><au>Kirwin, Carroll J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhalation teratology studies of n-butyl mercaptan in rats and mice</atitle><jtitle>Fundamental and applied toxicology</jtitle><addtitle>Fundam Appl Toxicol</addtitle><date>1987-02</date><risdate>1987</risdate><volume>8</volume><issue>2</issue><spage>170</spage><epage>178</epage><pages>170-178</pages><issn>0272-0590</issn><eissn>1095-6832</eissn><coden>FAATDF</coden><abstract>n-Butyl mercaptan (
n-BM) is used as a solvent and a chemical intermediate. Pregnant Charles River CD-1 mice and COBS CD rats were randomly assigned to a control group and to three
n-BM-exposed groups of 25 rats and 25 mice each. The animals were exposed by whole-body inhalation to mean
n-BM concentrations of 10, 68, or 152 ppm on a 6-hr daily exposure schedule. Rats were exposed on Gestation Days 6–19 and mice on Gestation Days 6–16. The control group was exposed to filtered air only on a comparable regimen. Cesarean sections were performed on all surviving mice on Gestation Day 17 and on all rats on Gestation Day 20. Seventeen of the
n-BM-treated mice died: 8 at the 68-ppm level and 9 at the 152-ppm level; none of the
n-BM-treated rats died. An increased postimplantation loss and increased early resorption occurred in mice exposed at 68 and 152 ppm, indicating embryotoxicity. An increased incidence of cleft palate was observed in mice exposed to 10 or 68 ppm which was not statistically significant. Total fetal abnormalities were statistically significantly different from controls at 68 ppm where maternal lethality was observed when based on the fetal unit although not when based on the litter unit. Rats exposed to 152 ppm or less demonstrated no terata.</abstract><cop>Boston, MA</cop><cop>San Diego, CA</cop><cop>New York, NY</cop><pub>Elsevier Science (USA)</pub><pmid>3556829</pmid><doi>10.1016/0272-0590(87)90115-1</doi><tpages>9</tpages></addata></record> |
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subjects | Abnormalities, Drug-Induced - pathology Administration, Inhalation Animals Biological and medical sciences Body Weight - drug effects Embryology: invertebrates and vertebrates. Teratology Female Fundamental and applied biological sciences. Psychology Mice Pregnancy Rats Rats, Inbred Strains Species Specificity Sulfhydryl Compounds - administration & dosage Sulfhydryl Compounds - toxicity Teratogens Teratology. Teratogens |
title | Inhalation teratology studies of n-butyl mercaptan in rats and mice |
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