DNA ADDUCTS AND INDUCTION OF SISTER CHROMATID EXCHANGES IN THE RAT FOLLOWING BENZO[B]FLUORANTHENE ADMINISTRATION

被引:14
作者
ROSS, JA
NELSON, GB
HOLDEN, KL
KLIGERMAN, AD
EREXSON, GL
BRYANT, MF
EARLEY, K
BEACH, AC
GUPTA, RC
NESNOW, S
机构
[1] US EPA, HLTH EFFECTS LAB, MUTAGENESIS & CELLULAR TOXICOL BRANCH, RES TRIANGLE PK, NC 27711 USA
[2] ENVIRONM HLTH RES & TESTING INC, RES TRIANGLE PK, NC 27709 USA
[3] UNIV KENTUCKY, DEPT PREVENT MED & ENVIRONM HLTH, LEXINGTON, KY 40506 USA
[4] UNIV KENTUCKY, GRAD CTR TOXICOL, LEXINGTON, KY 40506 USA
关键词
D O I
10.1093/carcin/13.10.1731
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Benzo[b]fluoranthene (B[b]F) was administered (100 mg/kg by i.p. injection) to male Sprague-Dawley rats. Lungs, livers and peripheral blood lymphocytes (PBLs) were harvested 1, 3, 5, 7, 14, 28 and 56 days after treatment. Several DNA adducts were observed in each tissue, with maximal levels occurring at approximately 7 days after treatment. Lung DNA exhibited consistently higher adduct levels than liver or PBL DNA. At 56 days after B[b]F administration, the adducts in liver and PBL DNA were present at < 10 amol/mug DNA, while in lung there were 100 amoles/mug DNA. No significant differences were observed between tissues in the types of adducts produced. Co-chromatography with synthetic standards showed that only a minor adduct produced in vivo is derived from trans-9,10-dihydro-9,10-dihydroxybenzo[b]fluoranthene-11,12-oxide. Sister chromatid exchanges (SCEs) from whole blood cultures were significantly increased relative to concurrent controls between 1 and 14 days after B[b]F administration, with maximum levels at 14 days. By 28 days after treatment, SCEs had essentially returned to control levels. SCE induction did not correlate with the amount of B[b]F-DNA adducts remaining in the PBLs at harvest time.
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页码:1731 / 1734
页数:4
相关论文
共 17 条
[1]   A STUDY OF CHEMICAL CARCINOGENESIS .41. IDENTIFICATION OF METABOLITES OF BENZO[B]FLUORANTHENE [J].
AMIN, S ;
LAVOIE, EJ ;
HECHT, SS .
CARCINOGENESIS, 1982, 3 (02) :171-174
[2]  
DEUTSCHWENZEL RP, 1983, JNCI-J NATL CANCER I, V71, P539
[3]   A MODIFIED MOUSE PERIPHERAL-BLOOD LYMPHOCYTE CULTURE SYSTEM FOR CYTOGENETIC ANALYSIS [J].
EREXSON, GL ;
KLIGERMAN, AD .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1987, 10 (04) :377-386
[4]   FORMATION AND TUMORIGENICITY OF BENZO[B]FLUORANTHENE METABOLITES IN MOUSE EPIDERMIS [J].
GEDDIE, JE ;
AMIN, S ;
HUIE, K ;
HECHT, SS .
CARCINOGENESIS, 1987, 8 (11) :1579-1584
[5]   NONRANDOM BINDING OF THE CARCINOGEN N-HYDROXY-2-ACETYLAMINOFLUORENE TO REPETITIVE SEQUENCES OF RAT-LIVER DNA INVIVO [J].
GUPTA, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (22) :6943-6947
[6]  
GUPTA RC, 1985, CANCER RES, V45, P5656
[7]   TUMORIGENIC ACTIVITY OF NONALTERNANT POLYNUCLEAR AROMATIC-HYDROCARBONS IN NEWBORN MICE [J].
LAVOIE, EJ ;
BRALEY, J ;
RICE, JE ;
RIVENSON, A .
CANCER LETTERS, 1987, 34 (01) :15-20
[8]  
RANDERATH K, 1967, METHODS ENZYMOLOGY A, V12, P323
[9]   NUCLEASE-P1-MEDIATED ENHANCEMENT OF SENSITIVITY OF P-32 POSTLABELING TEST FOR STRUCTURALLY DIVERSE DNA ADDUCTS [J].
REDDY, MV ;
RANDERATH, K .
CARCINOGENESIS, 1986, 7 (09) :1543-1551
[10]   DNA ADDUCTS IN RAT LUNG, LIVER AND PERIPHERAL-BLOOD LYMPHOCYTES PRODUCED BY IP ADMINISTRATION OF BENZO[A]PYRENE METABOLITES AND DERIVATIVES [J].
ROSS, J ;
NELSON, G ;
EREXSON, G ;
KLIGERMAN, A ;
EARLEY, K ;
GUPTA, RC ;
NESNOW, S .
CARCINOGENESIS, 1991, 12 (10) :1953-1955