Susceptible period for the teratogenicity of di- n-butyltin dichloride in rats

Pregnant rats were given di- n-butyltin dichloride (DBT) by gastric intubation at a dose of 20 mg/kg on days 7–9, 10–12 or 13–15 of pregnancy or at a dose of 20 or 40 mg/kg on day 6,7,8 or 9 of pregnancy. While treatment with DBT on days 7–9 was significantly and high teratogenic, no evidence of ter...

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Veröffentlicht in:Toxicology (Amsterdam) 1992, Vol.73 (1), p.81-92
Hauptverfasser: Ema, Makoto, Itami, Takafumi, Kawasaki, Hironoshin
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Itami, Takafumi
Kawasaki, Hironoshin
description Pregnant rats were given di- n-butyltin dichloride (DBT) by gastric intubation at a dose of 20 mg/kg on days 7–9, 10–12 or 13–15 of pregnancy or at a dose of 20 or 40 mg/kg on day 6,7,8 or 9 of pregnancy. While treatment with DBT on days 7–9 was significantly and high teratogenic, no evidence of teratogenicity was detected when DBT was given on days 10–12 or 13–15. Treatment on day 7 or 8 with both doses of DBT, but neither on day 6 or 9, resulted in an increased incidence of fetuses with malformations. The highest incidence of malformed fetuses occurred after treatment on day 8. The incidence of malformed fetuses was proportional to the dose of DBT. Anomaly of tail, anal atresia, club foot, omphalocele, deformity of the vertebral column, defect of the ribs and anophthalmia or microphthalmia were predominantly observed. It could be concluded that, following maternal exposure to DBT in rats, developing offspring are not susceptible to teratogenic effects of DBT on day 6 and that day 7 is the earliest susceptible period, day 8 is the highest susceptible period and day 9 is no longer a susceptible period for teratogenesis of DBT.
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While treatment with DBT on days 7–9 was significantly and high teratogenic, no evidence of teratogenicity was detected when DBT was given on days 10–12 or 13–15. Treatment on day 7 or 8 with both doses of DBT, but neither on day 6 or 9, resulted in an increased incidence of fetuses with malformations. The highest incidence of malformed fetuses occurred after treatment on day 8. The incidence of malformed fetuses was proportional to the dose of DBT. Anomaly of tail, anal atresia, club foot, omphalocele, deformity of the vertebral column, defect of the ribs and anophthalmia or microphthalmia were predominantly observed. It could be concluded that, following maternal exposure to DBT in rats, developing offspring are not susceptible to teratogenic effects of DBT on day 6 and that day 7 is the earliest susceptible period, day 8 is the highest susceptible period and day 9 is no longer a susceptible period for teratogenesis of DBT.</description><identifier>ISSN: 0300-483X</identifier><identifier>EISSN: 1879-3185</identifier><identifier>DOI: 10.1016/0300-483X(92)90172-B</identifier><identifier>PMID: 1589881</identifier><identifier>CODEN: TXICDD</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Animals ; Biological and medical sciences ; Di- n-butyltin dichloride ; Embryology: invertebrates and vertebrates. Teratology ; Female ; Fetal malformation ; Fundamental and applied biological sciences. 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While treatment with DBT on days 7–9 was significantly and high teratogenic, no evidence of teratogenicity was detected when DBT was given on days 10–12 or 13–15. Treatment on day 7 or 8 with both doses of DBT, but neither on day 6 or 9, resulted in an increased incidence of fetuses with malformations. The highest incidence of malformed fetuses occurred after treatment on day 8. The incidence of malformed fetuses was proportional to the dose of DBT. Anomaly of tail, anal atresia, club foot, omphalocele, deformity of the vertebral column, defect of the ribs and anophthalmia or microphthalmia were predominantly observed. It could be concluded that, following maternal exposure to DBT in rats, developing offspring are not susceptible to teratogenic effects of DBT on day 6 and that day 7 is the earliest susceptible period, day 8 is the highest susceptible period and day 9 is no longer a susceptible period for teratogenesis of DBT.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Di- n-butyltin dichloride</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Female</subject><subject>Fetal malformation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gestational Age</subject><subject>Organotin</subject><subject>Organotin Compounds - administration &amp; dosage</subject><subject>Organotin Compounds - toxicity</subject><subject>Pregnancy</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Susceptible period</subject><subject>Teratogenicity</subject><subject>Teratogens - toxicity</subject><subject>Teratology. 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Teratology</topic><topic>Female</topic><topic>Fetal malformation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gestational Age</topic><topic>Organotin</topic><topic>Organotin Compounds - administration &amp; dosage</topic><topic>Organotin Compounds - toxicity</topic><topic>Pregnancy</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Susceptible period</topic><topic>Teratogenicity</topic><topic>Teratogens - toxicity</topic><topic>Teratology. Teratogens</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ema, Makoto</creatorcontrib><creatorcontrib>Itami, Takafumi</creatorcontrib><creatorcontrib>Kawasaki, Hironoshin</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology (Amsterdam)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ema, Makoto</au><au>Itami, Takafumi</au><au>Kawasaki, Hironoshin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Susceptible period for the teratogenicity of di- n-butyltin dichloride in rats</atitle><jtitle>Toxicology (Amsterdam)</jtitle><addtitle>Toxicology</addtitle><date>1992</date><risdate>1992</risdate><volume>73</volume><issue>1</issue><spage>81</spage><epage>92</epage><pages>81-92</pages><issn>0300-483X</issn><eissn>1879-3185</eissn><coden>TXICDD</coden><abstract>Pregnant rats were given di- n-butyltin dichloride (DBT) by gastric intubation at a dose of 20 mg/kg on days 7–9, 10–12 or 13–15 of pregnancy or at a dose of 20 or 40 mg/kg on day 6,7,8 or 9 of pregnancy. While treatment with DBT on days 7–9 was significantly and high teratogenic, no evidence of teratogenicity was detected when DBT was given on days 10–12 or 13–15. Treatment on day 7 or 8 with both doses of DBT, but neither on day 6 or 9, resulted in an increased incidence of fetuses with malformations. The highest incidence of malformed fetuses occurred after treatment on day 8. The incidence of malformed fetuses was proportional to the dose of DBT. Anomaly of tail, anal atresia, club foot, omphalocele, deformity of the vertebral column, defect of the ribs and anophthalmia or microphthalmia were predominantly observed. 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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Biological and medical sciences
Di- n-butyltin dichloride
Embryology: invertebrates and vertebrates. Teratology
Female
Fetal malformation
Fundamental and applied biological sciences. Psychology
Gestational Age
Organotin
Organotin Compounds - administration & dosage
Organotin Compounds - toxicity
Pregnancy
Rat
Rats
Rats, Inbred Strains
Susceptible period
Teratogenicity
Teratogens - toxicity
Teratology. Teratogens
title Susceptible period for the teratogenicity of di- n-butyltin dichloride in rats
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