Role of trace elements in cadmium chloride uptake in hepatoma cell lines

被引:50
作者
Fotakis, George [1 ]
Timbrell, John A. [1 ]
机构
[1] Kings Coll London, Dept Pharm, London SE1 8WA, England
关键词
cadmium; iron; copper; calcium channel blockers; zinc; HTC cells; HepG2; cells;
D O I
10.1016/j.toxlet.2005.11.016
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Cadmium coexists with other metals in various products. Releases of cadmium in the environment occur in parallel to the release of other metals including copper, iron and zinc which also have an essential role in human homeostasis as they participate in various biochemical pathways. We studied the interaction of iron, copper, zinc and calcium channel blockers (nifedipine and veraparmil) with cadmium chloride in two hepatoma cell lines (HepG2 and HTC cells) in order to determine if these trace elements can affect CdCl2 uptake and interfere with its toxicity. Both cell lines were initially exposed to CdCl2 (0-200 mu M) for 2h and the uptake of the metal was determined. Cadmium chloride uptake by HepG2 and HTC cells shows an increase with increasing doses of the metal. Cells were also pretreated with 100 uM of FeCl2 or ZnCl2 or CuCl2 or with a nifedipine/verapamil (100 uM) mixture for 2h and then exposed to 200 uM CdCl2 for I h in the presence of the trace elements. The uptake of CdCl2 was determined as well as the membrane integrity (LDH leakage assay), the cell viability (neutral red assay) and cell proliferation (protein assay). Zinc and calcium channel blockers inhibited the uptake of cadmium chloride by both cell lines. On the other hand iron loading resulted in increased uptake of CdCl2 by both cell lines whereas copper loading increased the uptake of cadmium chloride from HTC cells and inhibited the uptake by HepG2 cells. These findings are of importance when the effects of cadmium on living organisms are examined since co-exposure to cadmium and other metals can occur. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:97 / 103
页数:7
相关论文
共 28 条
  • [21] Effects of Cd2+, Pb2+ and CH3Hg+ on high voltage-activated calcium currents in pheochromocytoma (PC12) cells:: potency, reversibility, interactions with extracellular Ca2+ and mechanisms of block
    Shafer, TJ
    [J]. TOXICOLOGY LETTERS, 1998, 99 (03) : 207 - 221
  • [22] Effect of cadmium on calcium transport in a human fetal hepatic cell line (WRL-68 cells)
    Souza, V
    Bucio, L
    Jay, D
    Chavez, E
    GutierrezRuiz, MC
    [J]. TOXICOLOGY, 1996, 112 (02) : 97 - 104
  • [23] DMT1 gene expression and cadmium absorption in human absorptive enterocytes
    Tallkvist, J
    Bowlus, CL
    Lönnerdal, B
    [J]. TOXICOLOGY LETTERS, 2001, 122 (02) : 171 - 177
  • [24] Effects of copper on the expression of metal transporters in human intestinal Caco-2 cells
    Tennant, J
    Stansfield, M
    Yamaji, S
    Srai, SK
    Sharp, P
    [J]. FEBS LETTERS, 2002, 527 (1-3): : 239 - 244
  • [25] Zn2+ and Cd2+ increase the cyclic GMP level in PC12 cells by inhibition of the cyclic nucleotide phosphodiesterase
    Wätjen, W
    Benters, J
    Haase, H
    Schwede, F
    Jastorff, B
    Beyersmann, D
    [J]. TOXICOLOGY, 2001, 157 (03) : 167 - 175
  • [26] Wispriyono B, 1998, J PHARMACOL EXP THER, V287, P344
  • [27] Zinc regulates the function and expression of the iron transporters DMT1 and IREG1 in human intestinal Caco-2 cells
    Yamaji, S
    Tennant, J
    Tandy, S
    Williams, M
    Srai, SKS
    Sharp, P
    [J]. FEBS LETTERS, 2001, 507 (02) : 137 - 141
  • [28] Effects of cadmium on electrolyte ions in cultured rat hepatocytes studied by X-ray microanalysis of cryosections
    Zierold, K
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1997, 144 (01) : 70 - 76