DNA single-strand breakage in rat lung, liver and kidney after single and combined treatments of nickel and cadmium

被引:38
作者
Saplakoglu, U
Iscan, M [1 ]
Iscan, M [1 ]
机构
[1] Middle E Tech Univ, Dept Biol, TR-06531 Ankara, Turkey
[2] Ankara Univ, Fac Pharm, Dept Toxicol, TR-06100 Ankara, Turkey
关键词
cadmium; nickel; DNA single-strand break; rats; combined exposure;
D O I
10.1016/S1383-5718(97)00134-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Single-strand breaks were observed in rat lung and kidney after acute treatment of animals with CdCl2 (4 mg/kg body weight) injected intraperitoneally and NiCl2 (44.4 mg/kg body weight) injected subcutaneously. In the rat liver, no single-strand breakage was evident with those doses in single and combined metal treatments. The most susceptible tissue in rats to cadmium or nickel chloride treatment was the lung tissue. The single-strand breaks were higher in cadmium treatment than in nickel treatment in the rat lung. Also the response to cadmium treatment was obtained earlier than nickel. Rat kidney was also responsive to cadmium treatment. However, the response, although statistically significant, was much lower than the one obtained in rat lung. The combined treatment, which was done by administrating cadmium prior to nickel administration, reduced the number of single-strand breaks significantly and reversed them to control values in rat lung and kidney. This study confirms that cadmium and nickel create single-strand breaks when administered alone in the rat lung. This effect, which was seen in the single metal treatments, was reduced in the combined treatments. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:133 / 140
页数:8
相关论文
共 32 条
[1]   INTERACTIONS IN METAL CARCINOGENICITY [J].
BEYERSMANN, D .
TOXICOLOGY LETTERS, 1994, 72 (1-3) :333-338
[2]   THE EFFECT OF NI(II) ON DNA-REPLICATION [J].
CHRISTIE, NT ;
TUMMOLO, DM .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1989, 21 :3-12
[3]  
CICCARELLI RB, 1982, CANCER RES, V42, P3544
[4]  
CICCARELLI RB, 1981, CANCER LETT, V12, P349, DOI 10.1016/0304-3835(81)90178-6
[5]   TOXICITY AND CARCINOGENICITY OF NICKEL COMPOUNDS [J].
COOGAN, TP ;
LATTA, DM ;
SNOW, ET ;
COSTA, M .
CRC CRITICAL REVIEWS IN TOXICOLOGY, 1989, 19 (04) :341-384
[6]   MOLECULAR MECHANISMS OF NICKEL CARCINOGENESIS [J].
COSTA, M ;
ZHUANG, ZX ;
HUANG, X ;
COSENTINO, S ;
KLEIN, CB ;
SALNIKOW, K .
SCIENCE OF THE TOTAL ENVIRONMENT, 1994, 148 (2-3) :191-199
[7]  
GUNN SA, 1964, P SOC EXP BIOL MED, V115, P653
[8]  
GUNN SA, 1963, J NATL CANCER I, V31, P745
[9]  
*IARC, 1994, IARC MON, V58, P119
[10]  
INT AGCY RES CANC, 1990, IARC MONOG EVAL CARC, V49, P257