Protection against arsenic trioxide-induced autophagic cell death in U118 human glioma cells by use of lipoic acid

被引:33
作者
Cheng, Tain-Junn
Wang, Ying-Jan
Kao, Wei-Wan
Chen, Rong-Jane
Ho, Yuan-Soon
机构
[1] Natl Cheng Kung Univ, Coll Med, Dept Environm & Occupat Hlth, Tainan 704, Taiwan
[2] Chimei Med Ctr, Tainan, Taiwan
[3] Taipei Med Univ, Grad Inst Biomed Technol, Taipei 110, Taiwan
关键词
lipoic acid; arsenic trioxide; neurotoxicity; autophage;
D O I
10.1016/j.fct.2006.12.014
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Arsenic is an environmental toxicant found naturally in ground water. Epidemiological studies have suggested a correlation between chronic arsenic exposure and potential brain tissue damage in clinical case and animal experiments. Lipoic acid (LA) is a thiol-compound naturally occurring in plants and animals, which is thought to be a strong antioxidant and possess neuroprotective effects. The objective of this study was to determine if the AS2O(3)-induced glial cell toxicity could be prevented by LA. The human malignant glioma cell (U118) was selected as a research model. By using acridine orange staining and flow cytometry analysis, we found that autophagic, but not apoptotic, cell death was significantly induced by AS2O(3) in U.118 cells, and that AS2O(3)-mediated autophagic cell death was nearly completely attenuated by LA. Down-regulation of p53 and Bax proteins and the up-regulation of Bcl-2 and HSP-70 proteins were observed by western blot in AS2O(3)-mediated autophagic cell death. Our results implied that LA completely inhibited U118 cells autophagic cell death induced by AS2O(3). We suggested that LA may emerge as a useful protective agent against arsenic-induced glial cell toxicity and reversing arsenic-induced damage in human brain. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1027 / 1038
页数:12
相关论文
共 58 条
  • [11] Chronic arsenic poisoning
    Hall, AH
    [J]. TOXICOLOGY LETTERS, 2002, 128 (1-3) : 69 - 72
  • [12] Acute arsenic poisoning treated by intravenous dimercaptosuccinic acid (DMSA) and combined extrarenal epuration techniques
    Hantson, P
    Haufroid, V
    Buchet, JP
    Mahieu, P
    [J]. JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY, 2003, 41 (01): : 1 - 6
  • [13] Ho YS, 1996, MOL CARCINOGEN, V16, P20, DOI 10.1002/(SICI)1098-2744(199605)16:1<20::AID-MC4>3.3.CO
  • [14] 2-I
  • [15] Jiang XH, 2001, INT J CANCER, V91, P173, DOI 10.1002/1097-0215(200002)9999:9999<::AID-IJC1039>3.0.CO
  • [16] 2-D
  • [17] Kanzawa T, 2003, CANCER RES, V63, P2103
  • [18] Arsenic trioxide induces autophagic cell death in malignant glioma cells by upregulation of mitochondrial cell death protein BNIP3
    Kanzawa, T
    Zhang, L
    Xiao, LC
    Germano, IM
    Kondo, Y
    Kondo, S
    [J]. ONCOGENE, 2005, 24 (06) : 980 - 991
  • [19] Arsenic trioxide-induced death of neuroblastoma cells involves activation of Bax and does not require p53
    Karlsson, J
    Ora, I
    Pörn-Ares, I
    Påhlman, S
    [J]. CLINICAL CANCER RESEARCH, 2004, 10 (09) : 3179 - 3188
  • [20] Kato K, 1997, CELL STRESS CHAPERON, V2, P199, DOI 10.1379/1466-1268(1997)002<0199:MOTAIE>2.3.CO