The Histology and Development of Hepatic Nodules and Carcinoma in C3H/He and C57BL/6 Mice Following Chronic Phenobarbitone Administration
Male C3H/He and C57BL/6 mice were given diets containing sodium phenobarbitone (PB) to allow a daily intake of 85 mg/kg. Control and treated animals were killed at 5, 30, 40, 60, and 80 wk. Other mice were killed in extremis or at the end of the respective experiments: 91 wk for C3H/He and 100 wk fo...
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description | Male C3H/He and C57BL/6 mice were given diets containing sodium phenobarbitone (PB) to allow a daily intake of 85 mg/kg. Control and treated animals were killed at 5, 30, 40, 60, and 80 wk. Other mice were killed in extremis or at the end of the respective experiments: 91 wk for C3H/He and 100 wk for the C57BL/6 animals. A basophilic nodule was found in 1/5 control C3H/He mice at 30 wk; these nodules increased in number with time so that nodules of this type were found in approximately 70% of animals by 91 wk. Nodules were not found in control C57BL/6 mice until 80 wk, when they were found in 4% of mice. PB treatment markedly increased the number of hepatic nodules in both strains of mice. The additional nodule burden was due to the development of a second nodule type formed of large cells with a predominantly eosinophilic cytoplasm. C3H/He animals given PB for 60 wk and then returned to a control diet bore fewer nodules at 91 wk than treated mice killed at 60 or 91 wk. The cumulative incidence of carcinoma in control C3H/He and C57BL/6 mice was 28 and 4%, respectively. The incidence of carcinoma was not increased by PB treatment in either strain. It is concluded that both strains of mice behave in a qualitively similar way to PB administration, although they show considerable quantitative differences in terms of the time and number of nodules that develop. Furthermore, the increased nodule numbers associated with PB treatment were not accompanied by an increase in the number of carcinomas. |
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Control and treated animals were killed at 5, 30, 40, 60, and 80 wk. Other mice were killed in extremis or at the end of the respective experiments: 91 wk for C3H/He and 100 wk for the C57BL/6 animals. A basophilic nodule was found in 1/5 control C3H/He mice at 30 wk; these nodules increased in number with time so that nodules of this type were found in approximately 70% of animals by 91 wk. Nodules were not found in control C57BL/6 mice until 80 wk, when they were found in 4% of mice. PB treatment markedly increased the number of hepatic nodules in both strains of mice. The additional nodule burden was due to the development of a second nodule type formed of large cells with a predominantly eosinophilic cytoplasm. C3H/He animals given PB for 60 wk and then returned to a control diet bore fewer nodules at 91 wk than treated mice killed at 60 or 91 wk. The cumulative incidence of carcinoma in control C3H/He and C57BL/6 mice was 28 and 4%, respectively. The incidence of carcinoma was not increased by PB treatment in either strain. It is concluded that both strains of mice behave in a qualitively similar way to PB administration, although they show considerable quantitative differences in terms of the time and number of nodules that develop. Furthermore, the increased nodule numbers associated with PB treatment were not accompanied by an increase in the number of carcinomas.</description><identifier>ISSN: 0192-6233</identifier><identifier>EISSN: 1533-1601</identifier><identifier>DOI: 10.1177/019262339202000405</identifier><identifier>PMID: 1308624</identifier><language>eng</language><publisher>Thousand Oaks, CA: SAGE Publications</publisher><subject>Animal tumors. Experimental tumors ; Animals ; Biological and medical sciences ; Experimental digestive system and abdominal tumors ; Life Sciences & Biomedicine ; Liver - cytology ; Liver - drug effects ; Liver Neoplasms, Experimental - chemically induced ; Liver Neoplasms, Experimental - pathology ; Male ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C3H ; Pathology ; Phenobarbital - toxicity ; Science & Technology ; Time Factors ; Toxicology ; Tumors</subject><ispartof>Toxicologic pathology, 1992-01, Vol.20 (4), p.585-594</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>27</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wosA1992LM50700005</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c465t-4f329c88ef8f12b9aa740a7f2708d1f957e0b75a1a6f370d048be34bfd2b92e3</citedby><cites>FETCH-LOGICAL-c465t-4f329c88ef8f12b9aa740a7f2708d1f957e0b75a1a6f370d048be34bfd2b92e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/019262339202000405$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/019262339202000405$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>315,781,785,21824,27197,27929,27930,43626,43627</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4816857$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1308624$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Evans, John G.</creatorcontrib><creatorcontrib>Collins, Michael A.</creatorcontrib><creatorcontrib>Lake, Brian G.</creatorcontrib><creatorcontrib>Butler, William H.</creatorcontrib><title>The Histology and Development of Hepatic Nodules and Carcinoma in C3H/He and C57BL/6 Mice Following Chronic Phenobarbitone Administration</title><title>Toxicologic pathology</title><addtitle>TOXICOL PATHOL</addtitle><addtitle>Toxicol Pathol</addtitle><description>Male C3H/He and C57BL/6 mice were given diets containing sodium phenobarbitone (PB) to allow a daily intake of 85 mg/kg. Control and treated animals were killed at 5, 30, 40, 60, and 80 wk. Other mice were killed in extremis or at the end of the respective experiments: 91 wk for C3H/He and 100 wk for the C57BL/6 animals. A basophilic nodule was found in 1/5 control C3H/He mice at 30 wk; these nodules increased in number with time so that nodules of this type were found in approximately 70% of animals by 91 wk. Nodules were not found in control C57BL/6 mice until 80 wk, when they were found in 4% of mice. PB treatment markedly increased the number of hepatic nodules in both strains of mice. The additional nodule burden was due to the development of a second nodule type formed of large cells with a predominantly eosinophilic cytoplasm. C3H/He animals given PB for 60 wk and then returned to a control diet bore fewer nodules at 91 wk than treated mice killed at 60 or 91 wk. The cumulative incidence of carcinoma in control C3H/He and C57BL/6 mice was 28 and 4%, respectively. The incidence of carcinoma was not increased by PB treatment in either strain. It is concluded that both strains of mice behave in a qualitively similar way to PB administration, although they show considerable quantitative differences in terms of the time and number of nodules that develop. Furthermore, the increased nodule numbers associated with PB treatment were not accompanied by an increase in the number of carcinomas.</description><subject>Animal tumors. Experimental tumors</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Experimental digestive system and abdominal tumors</subject><subject>Life Sciences & Biomedicine</subject><subject>Liver - cytology</subject><subject>Liver - drug effects</subject><subject>Liver Neoplasms, Experimental - chemically induced</subject><subject>Liver Neoplasms, Experimental - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C3H</subject><subject>Pathology</subject><subject>Phenobarbital - toxicity</subject><subject>Science & Technology</subject><subject>Time Factors</subject><subject>Toxicology</subject><subject>Tumors</subject><issn>0192-6233</issn><issn>1533-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EZCTM</sourceid><sourceid>EIF</sourceid><recordid>eNqNkM1u1DAURiMEKkPhBZCQvEBigcL4J46d5TRQgjQFFrOPHOd6xlViD3ZC1UfgrfE0o7JAQqws-Z7vu7ony14T_IEQIdaYVLSkjFUUU4xxgfmTbEU4YzkpMXmarU5AfiKeZy9ivMWYSFLgi-yCMCxLWqyyX7sDoMbGyQ9-f4-U69FH-AmDP47gJuQNauCoJqvRV9_PA8QHpFZBW-dHhaxDNWvWDSz_XFxt1yW6sRrQtR8Gf2fdHtWH4F2q-H4A5zsVOjt5B2jTj9al1SH1e_cye2bUEOHV-b3MdtefdnWTb799_lJvtrkuSj7lhWG00lKCkYbQrlJKFFgJQwWWPTEVF4A7wRVRpWEC97iQHbCiM32CKbDL7N1Sewz-xwxxakcbNQyDcuDn2ArOCZMl44mkC6mDjzGAaY_BjirctwS3J__t3_5T6M25fu5G6P9EFuFp_vY8V1GrwQTltI2PWCFJKblImFywO-i8idqC0_BIbUhV0e0NxyJtxby204PB2s9uStH3_x9N9Hqho9pDe-vn4JL8f134G4Gfuss</recordid><startdate>19920101</startdate><enddate>19920101</enddate><creator>Evans, John G.</creator><creator>Collins, Michael A.</creator><creator>Lake, Brian G.</creator><creator>Butler, William H.</creator><general>SAGE Publications</general><general>Soc Toxicologic Pathologists</general><general>Sage</general><scope>BLEPL</scope><scope>DTL</scope><scope>EZCTM</scope><scope>IQODW</scope><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>19920101</creationdate><title>The Histology and Development of Hepatic Nodules and Carcinoma in C3H/He and C57BL/6 Mice Following Chronic Phenobarbitone Administration</title><author>Evans, John G. ; Collins, Michael A. ; Lake, Brian G. ; Butler, William H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-4f329c88ef8f12b9aa740a7f2708d1f957e0b75a1a6f370d048be34bfd2b92e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animal tumors. Experimental tumors</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Experimental digestive system and abdominal tumors</topic><topic>Life Sciences & Biomedicine</topic><topic>Liver - cytology</topic><topic>Liver - drug effects</topic><topic>Liver Neoplasms, Experimental - chemically induced</topic><topic>Liver Neoplasms, Experimental - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C3H</topic><topic>Pathology</topic><topic>Phenobarbital - toxicity</topic><topic>Science & Technology</topic><topic>Time Factors</topic><topic>Toxicology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Evans, John G.</creatorcontrib><creatorcontrib>Collins, Michael A.</creatorcontrib><creatorcontrib>Lake, Brian G.</creatorcontrib><creatorcontrib>Butler, William H.</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 1992</collection><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>Toxicologic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Evans, John G.</au><au>Collins, Michael A.</au><au>Lake, Brian G.</au><au>Butler, William H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Histology and Development of Hepatic Nodules and Carcinoma in C3H/He and C57BL/6 Mice Following Chronic Phenobarbitone Administration</atitle><jtitle>Toxicologic pathology</jtitle><stitle>TOXICOL PATHOL</stitle><addtitle>Toxicol Pathol</addtitle><date>1992-01-01</date><risdate>1992</risdate><volume>20</volume><issue>4</issue><spage>585</spage><epage>594</epage><pages>585-594</pages><issn>0192-6233</issn><eissn>1533-1601</eissn><abstract>Male C3H/He and C57BL/6 mice were given diets containing sodium phenobarbitone (PB) to allow a daily intake of 85 mg/kg. Control and treated animals were killed at 5, 30, 40, 60, and 80 wk. Other mice were killed in extremis or at the end of the respective experiments: 91 wk for C3H/He and 100 wk for the C57BL/6 animals. A basophilic nodule was found in 1/5 control C3H/He mice at 30 wk; these nodules increased in number with time so that nodules of this type were found in approximately 70% of animals by 91 wk. Nodules were not found in control C57BL/6 mice until 80 wk, when they were found in 4% of mice. PB treatment markedly increased the number of hepatic nodules in both strains of mice. The additional nodule burden was due to the development of a second nodule type formed of large cells with a predominantly eosinophilic cytoplasm. C3H/He animals given PB for 60 wk and then returned to a control diet bore fewer nodules at 91 wk than treated mice killed at 60 or 91 wk. The cumulative incidence of carcinoma in control C3H/He and C57BL/6 mice was 28 and 4%, respectively. The incidence of carcinoma was not increased by PB treatment in either strain. It is concluded that both strains of mice behave in a qualitively similar way to PB administration, although they show considerable quantitative differences in terms of the time and number of nodules that develop. Furthermore, the increased nodule numbers associated with PB treatment were not accompanied by an increase in the number of carcinomas.</abstract><cop>Thousand Oaks, CA</cop><pub>SAGE Publications</pub><pmid>1308624</pmid><doi>10.1177/019262339202000405</doi><tpages>10</tpages></addata></record> |
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subjects | Animal tumors. Experimental tumors Animals Biological and medical sciences Experimental digestive system and abdominal tumors Life Sciences & Biomedicine Liver - cytology Liver - drug effects Liver Neoplasms, Experimental - chemically induced Liver Neoplasms, Experimental - pathology Male Medical sciences Mice Mice, Inbred BALB C Mice, Inbred C3H Pathology Phenobarbital - toxicity Science & Technology Time Factors Toxicology Tumors |
title | The Histology and Development of Hepatic Nodules and Carcinoma in C3H/He and C57BL/6 Mice Following Chronic Phenobarbitone Administration |
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