Genotoxic effects of aluminum chloride in cultured human lymphocytes treated in different phases of cell cycle

被引:78
作者
Lima, P. D. L.
Leite, D. S.
Vasconcellos, M. C.
Cavalcanti, B. C.
Santos, R. A.
Costa-Lotufo, L. V.
Pessoa, C.
Moraes, M. O.
Burbano, R. R. [1 ]
机构
[1] Fed Univ Para, Ctr Biol Sci, Dept Biol, Human Cytogenet Lab, BR-66059 Belem, Para, Brazil
[2] Univ Fed Ceara, Sch Med, Dept Physiol & Pharmcol, Fortaleza, Ceara, Brazil
[3] Univ Sao Paulo, Fac Med, Dept Genet, Ribeirao Preto, SP, Brazil
关键词
aluminum chloride; chromosome aberration; comet assay;
D O I
10.1016/j.fct.2006.12.022
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Aluminum (Al) is the most abundant metal and the third common chemical element on earth. It is known that Al is toxic, especially its trivalent form (Al3+), that represents the its most soluble form. Al intoxication is related to some pathogenic disorders, principally neurodegeneratives ones as Parkinson and Alzheimer diseases. The, present study aimed to evaluate the mutagenic potential of aluminum chloride (AlCl3). Comet assay and chromosome aberrations analysis were applied to evaluate the DNA-damaging and clastogenic effects of AlCl3, respectively, in different phases of the cell cycle. Cultured human lymphocytes were treated with 5, 10, 15 and 25 mu M aluminum chloride during the G 1, G 1/S, S (pulses of 1 and 6 h), and G2 phases of the cell cycle. All tested concentrations were cytotoxic and reduced significantly the mitotic index in all phases of cell cycle. They also induced DNA damage and were clastogenic in all phases of cell cycle, specially in S phase. AlCl3 also induced endoreduplication and polyploidy in treatments performed during G1 phase. The presence of genotoxicity and polyploidy on interphase and mitosis, respectively, suggests that aluminum chloride is clastogenic and indirectly affects the construction of mitotic fuse in all tested concentrations. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1154 / 1159
页数:6
相关论文
共 48 条
[21]   The contribution of cytotoxicity to DNA-effects in the single cell gel test (comet assay) [J].
Hartmann, A ;
Speit, G .
TOXICOLOGY LETTERS, 1997, 90 (2-3) :183-188
[22]   Viability of fibroblasts in cell culture after treatment with different chemical retraction agents [J].
Kopac, I ;
Batista, U ;
Cvetko, E ;
Marion, L .
JOURNAL OF ORAL REHABILITATION, 2002, 29 (01) :98-104
[23]   CHROMOSOME PREPARATIONS OF LEUKOCYTES CULTURED FROM HUMAN PERIPHERAL BLOOD [J].
MOORHEAD, PS ;
NOWELL, PC ;
MELLMAN, WJ ;
BATTIPS, DM ;
HUNGERFORD, DA .
EXPERIMENTAL CELL RESEARCH, 1960, 20 (03) :613-616
[24]  
Moreno EA, 1997, ARCH MED RES, V28, P549
[25]   Cytogenetic, developmental, and biochemical effects of aluminum, iron, and their mixture in sea urchins and mussels [J].
Pagano, G ;
His, E ;
Beiras, R ;
DeBiase, A ;
Korkina, LG ;
Iaccarino, M ;
Oral, R ;
Quiniou, F ;
Warnau, M ;
Trieff, NM .
ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1996, 31 (04) :466-474
[26]   Should gaps be included in chromosomal aberration analysis?: Evidence based on the comet assay [J].
Paz-y-Miño, C ;
Dávalos, MV ;
Sánchez, ME ;
Arévalo, M ;
Leone, PE .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 516 (1-2) :57-61
[27]  
PRESTON RJ, 1987, MUTAT RES, V189, P175
[28]   CELL DETACHMENT AND GROWTH OF FIBROBLASTS AS PARAMETERS FOR CYTO-TOXICITY OF INORGANIC METAL-SALTS INVITRO [J].
REINHARDT, CA ;
PELLI, DA ;
SANDVOLD, M .
CELL BIOLOGY AND TOXICOLOGY, 1985, 1 (02) :33-43
[29]   Aluminium in over-the-counter drugs - Risks outweigh benefits? [J].
Reinke, CM ;
Breitkreutz, J ;
Leuenberger, H .
DRUG SAFETY, 2003, 26 (14) :1011-1025
[30]   LYMPHOCYTE CHROMOSOME STUDIES IN HUMANS EXPOSED TO CHEMICAL MUTAGENS - VALIDITY OF METHOD IN 67 PATIENTS UNDER CYTOSTATIC THERAPY [J].
SCHINZEL, A ;
SCHMID, W .
MUTATION RESEARCH, 1976, 40 (02) :139-165