LONG-TERM EXPERIMENT OF MAXIMAL NON-CARCINOGENIC DOSE OF DIMETHYLNITROSAMINE FOR CARCINOGENESIS IN RATS
Studies were made on the maximal non-carcinogenic dose of dimethylnitrosamine (DMN) in rats. Groups of Wistar strain rats of both sexes, 6 weeks old, were given standard diet without DMN (group 1), or containing 0.1ppm DMN (group 2), 1.0ppm DMN (group 3), or 10ppm DMN (group 4) for 96 weeks and then...
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Veröffentlicht in: | GANN Japanese Journal of Cancer Research 1979/08/31, Vol.70(4), pp.549-558 |
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description | Studies were made on the maximal non-carcinogenic dose of dimethylnitrosamine (DMN) in rats. Groups of Wistar strain rats of both sexes, 6 weeks old, were given standard diet without DMN (group 1), or containing 0.1ppm DMN (group 2), 1.0ppm DMN (group 3), or 10ppm DMN (group 4) for 96 weeks and then sacrificed for hematological, serum-biochemical, and histopathological examinations. After 96 weeks, the weights of the body and main organs in the different groups were not significantly different. The leucocyte count and blood urea-nitrogen (BUN) in group 4 were slightly increased, but other serum findings were not significantly different in different groups. Hepatocellular carcinomas were found in group 3 (1 male and 3 females), but not in group 2. Hemangioendotheliomas of the liver, adrenal adenomas, pituitary adenomas, interstitial cell tumors of the testis, ovarian tumors, and leukemia were also found. Pyelonephritis was found in both experimental and control animals, but no kidney tumors developed with these dose levels of DMN. These results show that on long-term oral administration to rats, 1.0ppm DMN is the minimum carcinogenic dose, while a level of about 0.1ppm DMN is non-carcinogenic. |
doi_str_mv | 10.20772/cancersci1959.70.4_549 |
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Groups of Wistar strain rats of both sexes, 6 weeks old, were given standard diet without DMN (group 1), or containing 0.1ppm DMN (group 2), 1.0ppm DMN (group 3), or 10ppm DMN (group 4) for 96 weeks and then sacrificed for hematological, serum-biochemical, and histopathological examinations. After 96 weeks, the weights of the body and main organs in the different groups were not significantly different. The leucocyte count and blood urea-nitrogen (BUN) in group 4 were slightly increased, but other serum findings were not significantly different in different groups. Hepatocellular carcinomas were found in group 3 (1 male and 3 females), but not in group 2. Hemangioendotheliomas of the liver, adrenal adenomas, pituitary adenomas, interstitial cell tumors of the testis, ovarian tumors, and leukemia were also found. Pyelonephritis was found in both experimental and control animals, but no kidney tumors developed with these dose levels of DMN. These results show that on long-term oral administration to rats, 1.0ppm DMN is the minimum carcinogenic dose, while a level of about 0.1ppm DMN is non-carcinogenic.</description><identifier>ISSN: 0016-450X</identifier><identifier>DOI: 10.20772/cancersci1959.70.4_549</identifier><identifier>PMID: 510853</identifier><language>eng</language><publisher>Japan: The Japanese Cancer Association</publisher><subject>Animals ; Body Weight - drug effects ; Carcinogenesis ; Dimethylnitrosamine ; Dimethylnitrosamine - administration & dosage ; Dimethylnitrosamine - toxicity ; Dose-Response Relationship, Drug ; Female ; Liver Neoplasms, Experimental - chemically induced ; Male ; Maximum Allowable Concentration ; Maximum non-carcinogenic dose ; Rats ; Wistar rat</subject><ispartof>GANN Japanese Journal of Cancer Research, 1979/08/31, Vol.70(4), pp.549-558</ispartof><rights>The Japanese Cancer Association</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1876,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/510853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ARAI, Masayuki</creatorcontrib><creatorcontrib>AOKI, Yoshinari</creatorcontrib><creatorcontrib>NAKANISHI, Keisuke</creatorcontrib><creatorcontrib>MIYATA, Yukitada</creatorcontrib><creatorcontrib>MORI, Tomizo</creatorcontrib><creatorcontrib>ITO, Nobuyuki</creatorcontrib><title>LONG-TERM EXPERIMENT OF MAXIMAL NON-CARCINOGENIC DOSE OF DIMETHYLNITROSAMINE FOR CARCINOGENESIS IN RATS</title><title>GANN Japanese Journal of Cancer Research</title><addtitle>GANN Japanese Journal of Cancer Research</addtitle><description>Studies were made on the maximal non-carcinogenic dose of dimethylnitrosamine (DMN) in rats. Groups of Wistar strain rats of both sexes, 6 weeks old, were given standard diet without DMN (group 1), or containing 0.1ppm DMN (group 2), 1.0ppm DMN (group 3), or 10ppm DMN (group 4) for 96 weeks and then sacrificed for hematological, serum-biochemical, and histopathological examinations. After 96 weeks, the weights of the body and main organs in the different groups were not significantly different. The leucocyte count and blood urea-nitrogen (BUN) in group 4 were slightly increased, but other serum findings were not significantly different in different groups. Hepatocellular carcinomas were found in group 3 (1 male and 3 females), but not in group 2. Hemangioendotheliomas of the liver, adrenal adenomas, pituitary adenomas, interstitial cell tumors of the testis, ovarian tumors, and leukemia were also found. Pyelonephritis was found in both experimental and control animals, but no kidney tumors developed with these dose levels of DMN. These results show that on long-term oral administration to rats, 1.0ppm DMN is the minimum carcinogenic dose, while a level of about 0.1ppm DMN is non-carcinogenic.</description><subject>Animals</subject><subject>Body Weight - drug effects</subject><subject>Carcinogenesis</subject><subject>Dimethylnitrosamine</subject><subject>Dimethylnitrosamine - administration & dosage</subject><subject>Dimethylnitrosamine - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Liver Neoplasms, Experimental - chemically induced</subject><subject>Male</subject><subject>Maximum Allowable Concentration</subject><subject>Maximum non-carcinogenic dose</subject><subject>Rats</subject><subject>Wistar rat</subject><issn>0016-450X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMtqg0AUhmfRW0jzBoXOC5jO1dGlmEkyoDNFLaQrGXVME5IQNF307WuxNPQs_rP4Pg6cH4BnjOYECUFeanuqXdfXOxzycC7QnJWchTdgghD2PcbR5gHM-n6PhvGJIMK_B3cco4DTCdgmRq-8QmYplJtXmalU6gKaJUyjjUqjBGqjvTjKYqXNSmoVw4XJ5Y-wGNRi_Z5oVWQmj1KlJVyaDF5lmascKg2zqMgfwW1rD72b_e4peFvKIl57iVmpOEq8PcPhxWOI0QD7gW_DtuakxYHPnC9oyBkVAa2xIDWnDWscIS0SFXYBo7ghIXONreqKTsHTePf8WR1dU5673dF2X-X474DViPf9xW7dH7bdZVcfXPmvy1Kgko0xFHp1PmxXuhP9BjKEalI</recordid><startdate>19790101</startdate><enddate>19790101</enddate><creator>ARAI, Masayuki</creator><creator>AOKI, Yoshinari</creator><creator>NAKANISHI, Keisuke</creator><creator>MIYATA, Yukitada</creator><creator>MORI, Tomizo</creator><creator>ITO, Nobuyuki</creator><general>The Japanese Cancer Association</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19790101</creationdate><title>LONG-TERM EXPERIMENT OF MAXIMAL NON-CARCINOGENIC DOSE OF DIMETHYLNITROSAMINE FOR CARCINOGENESIS IN RATS</title><author>ARAI, Masayuki ; AOKI, Yoshinari ; NAKANISHI, Keisuke ; MIYATA, Yukitada ; MORI, Tomizo ; ITO, Nobuyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j419t-404381686a9fc52f1864e6739543783c172c53d4de22f07b1e8431d294edabcb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><topic>Animals</topic><topic>Body Weight - drug effects</topic><topic>Carcinogenesis</topic><topic>Dimethylnitrosamine</topic><topic>Dimethylnitrosamine - administration & dosage</topic><topic>Dimethylnitrosamine - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Liver Neoplasms, Experimental - chemically induced</topic><topic>Male</topic><topic>Maximum Allowable Concentration</topic><topic>Maximum non-carcinogenic dose</topic><topic>Rats</topic><topic>Wistar rat</topic><toplevel>online_resources</toplevel><creatorcontrib>ARAI, Masayuki</creatorcontrib><creatorcontrib>AOKI, Yoshinari</creatorcontrib><creatorcontrib>NAKANISHI, Keisuke</creatorcontrib><creatorcontrib>MIYATA, Yukitada</creatorcontrib><creatorcontrib>MORI, Tomizo</creatorcontrib><creatorcontrib>ITO, Nobuyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>GANN Japanese Journal of Cancer Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ARAI, Masayuki</au><au>AOKI, Yoshinari</au><au>NAKANISHI, Keisuke</au><au>MIYATA, Yukitada</au><au>MORI, Tomizo</au><au>ITO, Nobuyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LONG-TERM EXPERIMENT OF MAXIMAL NON-CARCINOGENIC DOSE OF DIMETHYLNITROSAMINE FOR CARCINOGENESIS IN RATS</atitle><jtitle>GANN Japanese Journal of Cancer Research</jtitle><addtitle>GANN Japanese Journal of Cancer Research</addtitle><date>1979-01-01</date><risdate>1979</risdate><volume>70</volume><issue>4</issue><spage>549</spage><epage>558</epage><pages>549-558</pages><issn>0016-450X</issn><abstract>Studies were made on the maximal non-carcinogenic dose of dimethylnitrosamine (DMN) in rats. Groups of Wistar strain rats of both sexes, 6 weeks old, were given standard diet without DMN (group 1), or containing 0.1ppm DMN (group 2), 1.0ppm DMN (group 3), or 10ppm DMN (group 4) for 96 weeks and then sacrificed for hematological, serum-biochemical, and histopathological examinations. After 96 weeks, the weights of the body and main organs in the different groups were not significantly different. The leucocyte count and blood urea-nitrogen (BUN) in group 4 were slightly increased, but other serum findings were not significantly different in different groups. Hepatocellular carcinomas were found in group 3 (1 male and 3 females), but not in group 2. Hemangioendotheliomas of the liver, adrenal adenomas, pituitary adenomas, interstitial cell tumors of the testis, ovarian tumors, and leukemia were also found. Pyelonephritis was found in both experimental and control animals, but no kidney tumors developed with these dose levels of DMN. These results show that on long-term oral administration to rats, 1.0ppm DMN is the minimum carcinogenic dose, while a level of about 0.1ppm DMN is non-carcinogenic.</abstract><cop>Japan</cop><pub>The Japanese Cancer Association</pub><pmid>510853</pmid><doi>10.20772/cancersci1959.70.4_549</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Body Weight - drug effects Carcinogenesis Dimethylnitrosamine Dimethylnitrosamine - administration & dosage Dimethylnitrosamine - toxicity Dose-Response Relationship, Drug Female Liver Neoplasms, Experimental - chemically induced Male Maximum Allowable Concentration Maximum non-carcinogenic dose Rats Wistar rat |
title | LONG-TERM EXPERIMENT OF MAXIMAL NON-CARCINOGENIC DOSE OF DIMETHYLNITROSAMINE FOR CARCINOGENESIS IN RATS |
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