Differential influences of various arsenic compounds on glutathione redox status and antioxidative enzymes in porcine endothelial cells

被引:50
作者
Yeh, JY
Cheng, LC
Ou, BR
Whanger, PD
Chang, LW
机构
[1] Natl Hlth Res Inst, Div Environm Hlth & Occupat Med, Kaohsiung 807, Taiwan
[2] Tunghai Univ, Dept Anim Sci, Taichung, Taiwan
[3] Oregon State Univ, Dept Environm & Mol Toxicol, Corvallis, OR USA
关键词
arsenic; antioxidative enzyme; glutathione redox status; hydrogen peroxide; porcine endothelial cell;
D O I
10.1007/PL00012519
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cellular response and detoxification mechanisms in porcine endothelial cells (PAECs) to arsenic trioxide (As2O3), sodium arsenite (NaAsO2) and sodium arsenate (Na2HAsO4,) were investigated. NaAsO2 at 20 muM for 72 h increased Cu/Zn superoxide dismutase activity resulting in elevated intracellular hydrogen peroxide levels, but As2O3 and Na2HAsO4 did not. Trivalent arsenic compounds increased intracellular oxidized glutathione (GSSG) and total glutathione (GSH) and cellular glutathione peroxidase (cGPX) and glutathione S-transferase (GST) activity, but not glutathione reductase activity. The increased cGPX activity resulted in an elevated cellular GSSG content. Na2HAsO4 increased the cellular GSSG level at 72 h compared to controls. These results imply that the increased GSH content responding to the oxidative stress by trivalent arsenic compounds may be mainly related to the regulation of GSH turnover. The increased GST activity implies that the elevated intracellular GSH level responding to the oxidative stress may be used to conjugate arsenic in PAECs and facilitate arsenic efflux.
引用
收藏
页码:1972 / 1982
页数:11
相关论文
共 49 条
[1]   Arsenic: Health effects, mechanisms of actions, and research issues [J].
Abernathy, CO ;
Liu, YP ;
Longfellow, D ;
Aposhian, HV ;
Beck, B ;
Fowler, B ;
Goyer, R ;
Menzer, R ;
Rossman, T ;
Thompson, C ;
Waalkes, M .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 (07) :593-597
[2]   Enzymatic methylation of arsenic species and other new approaches to arsenic toxicity [J].
Aposhian, HV .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1997, 37 :397-419
[3]  
Ballatori N, 1994, Adv Pharmacol, V27, P271, DOI 10.1016/S1054-3589(08)61036-4
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   Clinical management of women with genomic BRCA1 and BRCA2 mutations [J].
Chang, J ;
Elledge, RM .
BREAST CANCER RESEARCH AND TREATMENT, 2001, 69 (02) :101-113
[6]   INCREASED PREVALENCE OF HYPERTENSION AND LONG-TERM ARSENIC EXPOSURE [J].
CHEN, CJ ;
HSUEH, YM ;
LAI, MS ;
SHYU, MP ;
CHEN, SY ;
WU, MM ;
KUO, TL ;
TAI, TY .
HYPERTENSION, 1995, 25 (01) :53-60
[7]   Dose-response relationship between prevalence of cerebrovascular disease and ingested inorganic arsenic [J].
Chiou, HY ;
Huang, WI ;
Su, CL ;
Chang, SF ;
Hsu, YH ;
Chen, CJ .
STROKE, 1997, 28 (09) :1717-1723
[8]   In vitro effect of arsenical compounds on glutathione-related enzymes [J].
Chouchane, S ;
Snow, ET .
CHEMICAL RESEARCH IN TOXICOLOGY, 2001, 14 (05) :517-522
[9]   Malignant cells can be sensitized to undergo growth inhibition and apoptosis by arsenic trioxide through modulation of the glutathione redox system [J].
Dai, J ;
Weinberg, RS ;
Waxman, S ;
Jing, YK .
BLOOD, 1999, 93 (01) :268-277
[10]   TRANSFER OF ARSENITE FROM GLUTATHIONE TO DITHIOLS - A MODEL OF INTERACTION [J].
DELNOMDEDIEU, M ;
BASTI, MM ;
OTVOS, JD ;
THOMAS, DJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 1993, 6 (05) :598-602