Effect of an Aqueous Extract of Cigarette-Smoke Condensate on Benzo[a]pyrene-Induced Sarcoma and Body Weight in the Rat
An aqueous extract of cigarette-smoke condensate (AECSC) prepared from a commercial brand of cigarettes was administered in 10% sugar solution as drinking fluid to Sprague-Dawley female rats for 10 weeks starting at 30 days of age. Control groups drank the same volume of sugar solution as the groups...
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Veröffentlicht in: | JNCI : Journal of the National Cancer Institute 1972-04, Vol.48 (4), p.893-909 |
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description | An aqueous extract of cigarette-smoke condensate (AECSC) prepared from a commercial brand of cigarettes was administered in 10% sugar solution as drinking fluid to Sprague-Dawley female rats for 10 weeks starting at 30 days of age. Control groups drank the same volume of sugar solution as the groups given AECSC. Animals refused concentrations of AECSC higher than 1 mg/ml and all died of dehydration and starvation. At lower concentrations, 0.125–1.0 mg/ml, weight gain was directly related to the concentration of AECSC. Doses of benzo[a]pyrene (BP) ranging from 3–400 μg, dissolved in 0.1 ml sesame oil, were given subcutaneously on alternate days for 30 doses to 30-day-old rats. AECSC (0.25 mg/ml of 5% sugar solution) or 5% sugar solution alone was given as drinking fluid. Mean tumor-induction time was accelerated in 5 of 7 groups given AECSC, but all animals given doses of 12.5, 25, 100, 200, or 400 μg BP developed sarcoma at the site of injection within 5 months. At the 3-μg dose (total dose 90 μg) all rats that drank AECSC developed sarcoma in 235 ±15 (M ± SE) days; of 19 rats that drank the sugar solution, 9 had tumors in 272 ± 19 days and 10 were free of tumor when killed at 13 months of age. Under these conditions the dose-response curve for BP lies between 0 and 12.5 μg. These observations indicate that AECSC contains one or more components which function as a cocarcinogen. AECSC did not accelerate the induction time or increase the incidence of mammary tumors in rats fed BP. |
doi_str_mv | 10.1093/jnci/48.4.893 |
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Control groups drank the same volume of sugar solution as the groups given AECSC. Animals refused concentrations of AECSC higher than 1 mg/ml and all died of dehydration and starvation. At lower concentrations, 0.125–1.0 mg/ml, weight gain was directly related to the concentration of AECSC. Doses of benzo[a]pyrene (BP) ranging from 3–400 μg, dissolved in 0.1 ml sesame oil, were given subcutaneously on alternate days for 30 doses to 30-day-old rats. AECSC (0.25 mg/ml of 5% sugar solution) or 5% sugar solution alone was given as drinking fluid. Mean tumor-induction time was accelerated in 5 of 7 groups given AECSC, but all animals given doses of 12.5, 25, 100, 200, or 400 μg BP developed sarcoma at the site of injection within 5 months. At the 3-μg dose (total dose 90 μg) all rats that drank AECSC developed sarcoma in 235 ±15 (M ± SE) days; of 19 rats that drank the sugar solution, 9 had tumors in 272 ± 19 days and 10 were free of tumor when killed at 13 months of age. Under these conditions the dose-response curve for BP lies between 0 and 12.5 μg. These observations indicate that AECSC contains one or more components which function as a cocarcinogen. AECSC did not accelerate the induction time or increase the incidence of mammary tumors in rats fed BP.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/48.4.893</identifier><identifier>PMID: 5023687</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adenocarcinoma - chemically induced ; Adenocarcinoma, Papillary - chemically induced ; Adrenal Glands - anatomy & histology ; Animals ; Benzopyrenes ; Body Weight - drug effects ; Carcinogens ; Female ; Heart - anatomy & histology ; Hematocrit ; Hematopoiesis - drug effects ; Leukocyte Count ; Liver - anatomy & histology ; Lung - anatomy & histology ; Mammary Neoplasms, Experimental ; Nicotiana ; Organ Size ; Plants, Toxic ; Rats ; Sarcoma, Experimental - chemically induced ; Smoking ; Spleen - anatomy & histology ; Urinary Bladder Neoplasms - chemically induced</subject><ispartof>JNCI : Journal of the National Cancer Institute, 1972-04, Vol.48 (4), p.893-909</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5023687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sydnor, Katherine L.</creatorcontrib><creatorcontrib>Allen, Cheryl</creatorcontrib><creatorcontrib>Higgins, B.</creatorcontrib><title>Effect of an Aqueous Extract of Cigarette-Smoke Condensate on Benzo[a]pyrene-Induced Sarcoma and Body Weight in the Rat</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>Journal of the National Cancer Institute</addtitle><description>An aqueous extract of cigarette-smoke condensate (AECSC) prepared from a commercial brand of cigarettes was administered in 10% sugar solution as drinking fluid to Sprague-Dawley female rats for 10 weeks starting at 30 days of age. Control groups drank the same volume of sugar solution as the groups given AECSC. Animals refused concentrations of AECSC higher than 1 mg/ml and all died of dehydration and starvation. At lower concentrations, 0.125–1.0 mg/ml, weight gain was directly related to the concentration of AECSC. Doses of benzo[a]pyrene (BP) ranging from 3–400 μg, dissolved in 0.1 ml sesame oil, were given subcutaneously on alternate days for 30 doses to 30-day-old rats. AECSC (0.25 mg/ml of 5% sugar solution) or 5% sugar solution alone was given as drinking fluid. Mean tumor-induction time was accelerated in 5 of 7 groups given AECSC, but all animals given doses of 12.5, 25, 100, 200, or 400 μg BP developed sarcoma at the site of injection within 5 months. At the 3-μg dose (total dose 90 μg) all rats that drank AECSC developed sarcoma in 235 ±15 (M ± SE) days; of 19 rats that drank the sugar solution, 9 had tumors in 272 ± 19 days and 10 were free of tumor when killed at 13 months of age. Under these conditions the dose-response curve for BP lies between 0 and 12.5 μg. These observations indicate that AECSC contains one or more components which function as a cocarcinogen. AECSC did not accelerate the induction time or increase the incidence of mammary tumors in rats fed BP.</description><subject>Adenocarcinoma - chemically induced</subject><subject>Adenocarcinoma, Papillary - chemically induced</subject><subject>Adrenal Glands - anatomy & histology</subject><subject>Animals</subject><subject>Benzopyrenes</subject><subject>Body Weight - drug effects</subject><subject>Carcinogens</subject><subject>Female</subject><subject>Heart - anatomy & histology</subject><subject>Hematocrit</subject><subject>Hematopoiesis - drug effects</subject><subject>Leukocyte Count</subject><subject>Liver - anatomy & histology</subject><subject>Lung - anatomy & histology</subject><subject>Mammary Neoplasms, Experimental</subject><subject>Nicotiana</subject><subject>Organ Size</subject><subject>Plants, Toxic</subject><subject>Rats</subject><subject>Sarcoma, Experimental - chemically induced</subject><subject>Smoking</subject><subject>Spleen - anatomy & histology</subject><subject>Urinary Bladder Neoplasms - chemically induced</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1972</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j1FLwzAYRYMoc04ffRTyB7KlSdo0j1uZ29xEcANFkZKmX7dOm842xc1fb2HD-3LhHjhwEbr1aN-jig-21uQDEfZFP1T8DHU9EVDCPOqfoy6lTJIwlOISXdX1lrZRTHRQx6eMB6Hsop9xloFxuMywtnj43UDZ1Hi8d5U-rlG-1hU4B2RZlJ-Ao9KmYGvtAJcWj8D-lu_6Y3eowAKZ2bQxkOKlrkxZ6FaZ4lGZHvAL5OuNw7nFbgP4WbtrdJHprxpuTt1Dq_vxKpqSxdNkFg0XJGdCOKK48YELZjLwMyqVbFdjshCoZABKKKCCSplAoHzus1QliYFAm8DLEmNS3kN3R-2uSQpI412VF7o6xKf_LSdHntcO9v9YV59xILn04-nrW_ww59Fy_ujHE_4Hz9ZtTA</recordid><startdate>197204</startdate><enddate>197204</enddate><creator>Sydnor, Katherine L.</creator><creator>Allen, Cheryl</creator><creator>Higgins, B.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>197204</creationdate><title>Effect of an Aqueous Extract of Cigarette-Smoke Condensate on Benzo[a]pyrene-Induced Sarcoma and Body Weight in the Rat</title><author>Sydnor, Katherine L. ; Allen, Cheryl ; Higgins, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i244t-93c5e342cfe5f0797244ccf8e072ee949e04077be695352d9bbce6ac61fbccd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1972</creationdate><topic>Adenocarcinoma - chemically induced</topic><topic>Adenocarcinoma, Papillary - chemically induced</topic><topic>Adrenal Glands - anatomy & histology</topic><topic>Animals</topic><topic>Benzopyrenes</topic><topic>Body Weight - drug effects</topic><topic>Carcinogens</topic><topic>Female</topic><topic>Heart - anatomy & histology</topic><topic>Hematocrit</topic><topic>Hematopoiesis - drug effects</topic><topic>Leukocyte Count</topic><topic>Liver - anatomy & histology</topic><topic>Lung - anatomy & histology</topic><topic>Mammary Neoplasms, Experimental</topic><topic>Nicotiana</topic><topic>Organ Size</topic><topic>Plants, Toxic</topic><topic>Rats</topic><topic>Sarcoma, Experimental - chemically induced</topic><topic>Smoking</topic><topic>Spleen - anatomy & histology</topic><topic>Urinary Bladder Neoplasms - chemically induced</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sydnor, Katherine L.</creatorcontrib><creatorcontrib>Allen, Cheryl</creatorcontrib><creatorcontrib>Higgins, B.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sydnor, Katherine L.</au><au>Allen, Cheryl</au><au>Higgins, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of an Aqueous Extract of Cigarette-Smoke Condensate on Benzo[a]pyrene-Induced Sarcoma and Body Weight in the Rat</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>Journal of the National Cancer Institute</addtitle><date>1972-04</date><risdate>1972</risdate><volume>48</volume><issue>4</issue><spage>893</spage><epage>909</epage><pages>893-909</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>An aqueous extract of cigarette-smoke condensate (AECSC) prepared from a commercial brand of cigarettes was administered in 10% sugar solution as drinking fluid to Sprague-Dawley female rats for 10 weeks starting at 30 days of age. Control groups drank the same volume of sugar solution as the groups given AECSC. Animals refused concentrations of AECSC higher than 1 mg/ml and all died of dehydration and starvation. At lower concentrations, 0.125–1.0 mg/ml, weight gain was directly related to the concentration of AECSC. Doses of benzo[a]pyrene (BP) ranging from 3–400 μg, dissolved in 0.1 ml sesame oil, were given subcutaneously on alternate days for 30 doses to 30-day-old rats. AECSC (0.25 mg/ml of 5% sugar solution) or 5% sugar solution alone was given as drinking fluid. Mean tumor-induction time was accelerated in 5 of 7 groups given AECSC, but all animals given doses of 12.5, 25, 100, 200, or 400 μg BP developed sarcoma at the site of injection within 5 months. At the 3-μg dose (total dose 90 μg) all rats that drank AECSC developed sarcoma in 235 ±15 (M ± SE) days; of 19 rats that drank the sugar solution, 9 had tumors in 272 ± 19 days and 10 were free of tumor when killed at 13 months of age. Under these conditions the dose-response curve for BP lies between 0 and 12.5 μg. These observations indicate that AECSC contains one or more components which function as a cocarcinogen. AECSC did not accelerate the induction time or increase the incidence of mammary tumors in rats fed BP.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>5023687</pmid><doi>10.1093/jnci/48.4.893</doi><tpages>17</tpages></addata></record> |
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subjects | Adenocarcinoma - chemically induced Adenocarcinoma, Papillary - chemically induced Adrenal Glands - anatomy & histology Animals Benzopyrenes Body Weight - drug effects Carcinogens Female Heart - anatomy & histology Hematocrit Hematopoiesis - drug effects Leukocyte Count Liver - anatomy & histology Lung - anatomy & histology Mammary Neoplasms, Experimental Nicotiana Organ Size Plants, Toxic Rats Sarcoma, Experimental - chemically induced Smoking Spleen - anatomy & histology Urinary Bladder Neoplasms - chemically induced |
title | Effect of an Aqueous Extract of Cigarette-Smoke Condensate on Benzo[a]pyrene-Induced Sarcoma and Body Weight in the Rat |
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