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HIGHER SUSCEPTIBILITY OF NEWBORN THAN YOUNG RATS TO 3-METHYLPHENOL
To determine susceptibility of infants to 3-methylphenol, a repeated dose toxicity study was conducted with oral administration to newborn and young rats. In an 18-day newborn study from postnatal days 4 to 21 at doses of 30, 100 and 300 mg/kg/day, various clinical signs including deep respiration,...
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Published in: | Journal of toxicological sciences 2003, Vol.28(2), pp.59-70 |
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description | To determine susceptibility of infants to 3-methylphenol, a repeated dose toxicity study was conducted with oral administration to newborn and young rats. In an 18-day newborn study from postnatal days 4 to 21 at doses of 30, 100 and 300 mg/kg/day, various clinical signs including deep respiration, hypersensitivity on handling and tremors under contact stimulus, and depressed body weight gain were observed at 300 mg/kg. At 100 mg/kg, hypersensitivity and tremors were also noted in a small number of males only on single days during the dosing period. No adverse effects were observed in the 30 mg/kg group. There were no abnormalities of physical development, sexual maturation and reflex ontogeny. The no observed adverse effect level (NOAEL) for newborn rats was considered to be 30 mg/kg/day and the unequivocally toxic level 300 mg/kg/day. In a 28-day study starting at 5 weeks of age, clinical signs and depression of body weight gain, as observed in the newborn rats, appeared in both sexes at 1000 mg/kg but not 300 mg/kg. The NOAEL and the unequivocally toxic level were 300 mg/kg/day and 1,000 mg/kg/day, respectively. From these results, newborn rats were concluded to be 3 to 10 times more susceptible to 3-methylphenol than young rats. However, the realistic no adverse effect dose for the newborn must be slightly lower than 100 mg/kg/day, at which the toxicity incidence was very low, rather than 30 mg/kg/day. Based on this speculation and the equal toxicity at unequivocally toxic levels, the differences in the susceptibility to 3-methylphenol could be concluded to be 3 to 4 times. This is consistent with the results of our previous comparative studies on 4-nitrophenol, 2,4-dinitrophenol and 3-aminophenol, which showed 2 to 4 times differences in the susceptibility between newborn and young rats. |
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In an 18-day newborn study from postnatal days 4 to 21 at doses of 30, 100 and 300 mg/kg/day, various clinical signs including deep respiration, hypersensitivity on handling and tremors under contact stimulus, and depressed body weight gain were observed at 300 mg/kg. At 100 mg/kg, hypersensitivity and tremors were also noted in a small number of males only on single days during the dosing period. No adverse effects were observed in the 30 mg/kg group. There were no abnormalities of physical development, sexual maturation and reflex ontogeny. The no observed adverse effect level (NOAEL) for newborn rats was considered to be 30 mg/kg/day and the unequivocally toxic level 300 mg/kg/day. In a 28-day study starting at 5 weeks of age, clinical signs and depression of body weight gain, as observed in the newborn rats, appeared in both sexes at 1000 mg/kg but not 300 mg/kg. The NOAEL and the unequivocally toxic level were 300 mg/kg/day and 1,000 mg/kg/day, respectively. From these results, newborn rats were concluded to be 3 to 10 times more susceptible to 3-methylphenol than young rats. However, the realistic no adverse effect dose for the newborn must be slightly lower than 100 mg/kg/day, at which the toxicity incidence was very low, rather than 30 mg/kg/day. Based on this speculation and the equal toxicity at unequivocally toxic levels, the differences in the susceptibility to 3-methylphenol could be concluded to be 3 to 4 times. This is consistent with the results of our previous comparative studies on 4-nitrophenol, 2,4-dinitrophenol and 3-aminophenol, which showed 2 to 4 times differences in the susceptibility between newborn and young rats.</description><identifier>ISSN: 0388-1350</identifier><identifier>EISSN: 1880-3989</identifier><identifier>DOI: 10.2131/jts.28.59</identifier><identifier>PMID: 12820538</identifier><language>eng</language><publisher>Japan: The Japanese Society of Toxicology</publisher><subject>3-Methylphenol ; Aging - physiology ; Animals ; Animals, Newborn - physiology ; Blood Chemical Analysis ; Body Weight - drug effects ; Cresols - toxicity ; Female ; Male ; No-Observed-Adverse-Effect Level ; Organ Size - drug effects ; Pregnancy ; Rats ; Rats, Sprague-Dawley ; Sex Characteristics ; Toxicity in newborn rats</subject><ispartof>The Journal of Toxicological Sciences, 2003, Vol.28(2), pp.59-70</ispartof><rights>2003 The Japanese Society of Toxicology</rights><rights>Copyright Japan Science and Technology Agency 2003</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4929-a39a3e21e0d50cd5e30b85b46481c6598fe6a6f64aa3107cb6ebaa17e546dca33</citedby><cites>FETCH-LOGICAL-c4929-a39a3e21e0d50cd5e30b85b46481c6598fe6a6f64aa3107cb6ebaa17e546dca33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12820538$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KOIZUMI, Mutsuko</creatorcontrib><creatorcontrib>NODA, Atsushi</creatorcontrib><creatorcontrib>ITO, Yoshihiko</creatorcontrib><creatorcontrib>FURUKAWA, Masatoshi</creatorcontrib><creatorcontrib>FUJII, Sakiko</creatorcontrib><creatorcontrib>KAMATA, Eiichi</creatorcontrib><creatorcontrib>EMA, Makoto</creatorcontrib><creatorcontrib>HASEGAWA, Ryuichi</creatorcontrib><title>HIGHER SUSCEPTIBILITY OF NEWBORN THAN YOUNG RATS TO 3-METHYLPHENOL</title><title>Journal of toxicological sciences</title><addtitle>J Toxicol Sci</addtitle><description>To determine susceptibility of infants to 3-methylphenol, a repeated dose toxicity study was conducted with oral administration to newborn and young rats. In an 18-day newborn study from postnatal days 4 to 21 at doses of 30, 100 and 300 mg/kg/day, various clinical signs including deep respiration, hypersensitivity on handling and tremors under contact stimulus, and depressed body weight gain were observed at 300 mg/kg. At 100 mg/kg, hypersensitivity and tremors were also noted in a small number of males only on single days during the dosing period. No adverse effects were observed in the 30 mg/kg group. There were no abnormalities of physical development, sexual maturation and reflex ontogeny. The no observed adverse effect level (NOAEL) for newborn rats was considered to be 30 mg/kg/day and the unequivocally toxic level 300 mg/kg/day. In a 28-day study starting at 5 weeks of age, clinical signs and depression of body weight gain, as observed in the newborn rats, appeared in both sexes at 1000 mg/kg but not 300 mg/kg. The NOAEL and the unequivocally toxic level were 300 mg/kg/day and 1,000 mg/kg/day, respectively. From these results, newborn rats were concluded to be 3 to 10 times more susceptible to 3-methylphenol than young rats. However, the realistic no adverse effect dose for the newborn must be slightly lower than 100 mg/kg/day, at which the toxicity incidence was very low, rather than 30 mg/kg/day. Based on this speculation and the equal toxicity at unequivocally toxic levels, the differences in the susceptibility to 3-methylphenol could be concluded to be 3 to 4 times. This is consistent with the results of our previous comparative studies on 4-nitrophenol, 2,4-dinitrophenol and 3-aminophenol, which showed 2 to 4 times differences in the susceptibility between newborn and young rats.</description><subject>3-Methylphenol</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Animals, Newborn - physiology</subject><subject>Blood Chemical Analysis</subject><subject>Body Weight - drug effects</subject><subject>Cresols - toxicity</subject><subject>Female</subject><subject>Male</subject><subject>No-Observed-Adverse-Effect Level</subject><subject>Organ Size - drug effects</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sex Characteristics</subject><subject>Toxicity in newborn rats</subject><issn>0388-1350</issn><issn>1880-3989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpd0MtKw0AUBuBBFFurC19AAoLgInWu6cxGaEvaBGJS2hTpaphMp9rQm5lk4dubklrBzTmL8_Fz-AG4R7CLEUEveWm7mHeZuABtxDl0ieDiErQh4dxFhMEWuLE2hxD3IKPXoIUwx5AR3gaDIBwH_tSZzWdDf5KGgzAK04WTjJzYfx8k09hJg37sLJJ5PHam_XTmpIlD3Dc_DRbRJPDjJLoFVyu1sebutDtgPvLTYeBGyTgc9iNXU4GFq4hQxGBk4JJBvWSGwIyzjHqUI-0xwVfGU97Ko0oRBHs680ymFOoZRr2lVoR0wFOTeyj2X5WxpdyurTabjdqZfWUl4pAIRI_w8R_M91Wxq3-TiHqc94QQtFbPjdLF3trCrOShWG9V8S0RlMdaZV2rxFwyUduHU2KVbc3yT556rMFrA3Jbqg9zBqoo13pjfqNwM5g4H_SnKqTZkR-gL4Jx</recordid><startdate>2003</startdate><enddate>2003</enddate><creator>KOIZUMI, Mutsuko</creator><creator>NODA, Atsushi</creator><creator>ITO, Yoshihiko</creator><creator>FURUKAWA, Masatoshi</creator><creator>FUJII, Sakiko</creator><creator>KAMATA, Eiichi</creator><creator>EMA, Makoto</creator><creator>HASEGAWA, Ryuichi</creator><general>The Japanese Society of Toxicology</general><general>Japan Science and Technology Agency</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>7ST</scope><scope>7U7</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>2003</creationdate><title>HIGHER SUSCEPTIBILITY OF NEWBORN THAN YOUNG RATS TO 3-METHYLPHENOL</title><author>KOIZUMI, Mutsuko ; NODA, Atsushi ; ITO, Yoshihiko ; FURUKAWA, Masatoshi ; FUJII, Sakiko ; KAMATA, Eiichi ; EMA, Makoto ; HASEGAWA, Ryuichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4929-a39a3e21e0d50cd5e30b85b46481c6598fe6a6f64aa3107cb6ebaa17e546dca33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>3-Methylphenol</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Animals, Newborn - physiology</topic><topic>Blood Chemical Analysis</topic><topic>Body Weight - drug effects</topic><topic>Cresols - toxicity</topic><topic>Female</topic><topic>Male</topic><topic>No-Observed-Adverse-Effect Level</topic><topic>Organ Size - drug effects</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sex Characteristics</topic><topic>Toxicity in newborn rats</topic><toplevel>online_resources</toplevel><creatorcontrib>KOIZUMI, Mutsuko</creatorcontrib><creatorcontrib>NODA, Atsushi</creatorcontrib><creatorcontrib>ITO, Yoshihiko</creatorcontrib><creatorcontrib>FURUKAWA, Masatoshi</creatorcontrib><creatorcontrib>FUJII, Sakiko</creatorcontrib><creatorcontrib>KAMATA, Eiichi</creatorcontrib><creatorcontrib>EMA, Makoto</creatorcontrib><creatorcontrib>HASEGAWA, Ryuichi</creatorcontrib><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Journal of toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KOIZUMI, Mutsuko</au><au>NODA, Atsushi</au><au>ITO, Yoshihiko</au><au>FURUKAWA, Masatoshi</au><au>FUJII, Sakiko</au><au>KAMATA, Eiichi</au><au>EMA, Makoto</au><au>HASEGAWA, Ryuichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HIGHER SUSCEPTIBILITY OF NEWBORN THAN YOUNG RATS TO 3-METHYLPHENOL</atitle><jtitle>Journal of toxicological sciences</jtitle><addtitle>J Toxicol Sci</addtitle><date>2003</date><risdate>2003</risdate><volume>28</volume><issue>2</issue><spage>59</spage><epage>70</epage><pages>59-70</pages><issn>0388-1350</issn><eissn>1880-3989</eissn><abstract>To determine susceptibility of infants to 3-methylphenol, a repeated dose toxicity study was conducted with oral administration to newborn and young rats. In an 18-day newborn study from postnatal days 4 to 21 at doses of 30, 100 and 300 mg/kg/day, various clinical signs including deep respiration, hypersensitivity on handling and tremors under contact stimulus, and depressed body weight gain were observed at 300 mg/kg. At 100 mg/kg, hypersensitivity and tremors were also noted in a small number of males only on single days during the dosing period. No adverse effects were observed in the 30 mg/kg group. There were no abnormalities of physical development, sexual maturation and reflex ontogeny. The no observed adverse effect level (NOAEL) for newborn rats was considered to be 30 mg/kg/day and the unequivocally toxic level 300 mg/kg/day. In a 28-day study starting at 5 weeks of age, clinical signs and depression of body weight gain, as observed in the newborn rats, appeared in both sexes at 1000 mg/kg but not 300 mg/kg. The NOAEL and the unequivocally toxic level were 300 mg/kg/day and 1,000 mg/kg/day, respectively. From these results, newborn rats were concluded to be 3 to 10 times more susceptible to 3-methylphenol than young rats. However, the realistic no adverse effect dose for the newborn must be slightly lower than 100 mg/kg/day, at which the toxicity incidence was very low, rather than 30 mg/kg/day. Based on this speculation and the equal toxicity at unequivocally toxic levels, the differences in the susceptibility to 3-methylphenol could be concluded to be 3 to 4 times. This is consistent with the results of our previous comparative studies on 4-nitrophenol, 2,4-dinitrophenol and 3-aminophenol, which showed 2 to 4 times differences in the susceptibility between newborn and young rats.</abstract><cop>Japan</cop><pub>The Japanese Society of Toxicology</pub><pmid>12820538</pmid><doi>10.2131/jts.28.59</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3-Methylphenol Aging - physiology Animals Animals, Newborn - physiology Blood Chemical Analysis Body Weight - drug effects Cresols - toxicity Female Male No-Observed-Adverse-Effect Level Organ Size - drug effects Pregnancy Rats Rats, Sprague-Dawley Sex Characteristics Toxicity in newborn rats |
title | HIGHER SUSCEPTIBILITY OF NEWBORN THAN YOUNG RATS TO 3-METHYLPHENOL |
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