Phase II antioxidant enzyme activities in brain of male and female ACI rats treated chronically with estradiol

被引:12
作者
Stakhiv, Timothy M.
Mesia-Vela, Sonia
Kauffman, Frederick C.
机构
[1] Rutgers State Univ, Lab Cellular & Biochem Toxicol, Joint Grad Program Toxicol, Piscataway, NJ 08854 USA
[2] Univ Med & Dent New Jersey, Piscataway, NJ 08854 USA
关键词
estradiol; phase II antioxidant enzyme; reactive oxygen specie; ACI rat; phenol sulfotransferase; striatum;
D O I
10.1016/j.brainres.2006.05.093
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activities of Phase II antioxidant enzymes, including NAD(P)H:quinone oxidoreductase 1 (NQO1), glutathione S-transferase (GST), UDP-glucuronosyltransferase (UGT), and phenol sulfotransferase 1A1 (SULT1A1) were measured in brain of August-Copenhagen Irish (ACI) rats exposed chronically to low doses of estradiol (E-2). ACI rats were selected for study because this strain is highly responsive to treatment with low doses of E-2 as indexed by a high incidence of E-2-induced mammary tumors compared to other strains. Rats were exposed chronically to 3 mg E-2 contained in cholesterol pellets implanted subcutaneously for 6 weeks. This treatment increased activities of all four enzymes in the striatum of male but not female ACI rats. Blood E-2 levels at time of sacrifice correlated closely with activities of striatal NQO1, GST, and SULT1A1, but not with striatal UGT. NQO1, GST, and SULT1A1 activities in other brain regions including the cortex, cerebellum, and hippocampus were less sensitive to chronic E2 treatment. NQO1 was primarily localized in vascular elements and neurons and SULT1A1 primarily in neurons and neuropil of control and E-2-treated rats. Collectively, these results suggest that enhanced expression of NQO1, GST, and SULT1A1 may contribute to the antioxidant effects of E-2 in the striatum, an area of the brain that may be particularly prone to oxidative stress because of its high content of catecholamines. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:80 / 91
页数:12
相关论文
共 59 条
[1]   Regulatory mechanisms involved in activator-protein-1 (AP-1)-mediated activation of glutathione-S-transferase gene expression by chemical agents [J].
Ainbinder, E ;
Bergelson, S ;
Pinkus, R ;
Daniel, V .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 243 (1-2) :49-57
[2]  
Azcoitia I, 1999, J NEUROSCI RES, V58, P815, DOI 10.1002/(SICI)1097-4547(19991215)58:6<815::AID-JNR8>3.0.CO
[3]  
2-R
[4]   Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson's disease [J].
Blum, D ;
Torch, S ;
Lambeng, N ;
Nissou, MF ;
Benabid, AL ;
Sadoul, R ;
Verna, JM .
PROGRESS IN NEUROBIOLOGY, 2001, 65 (02) :135-172
[5]  
Buckmaster PS, 1997, J COMP NEUROL, V385, P385
[6]   Evaluation of the protective effect of oestradiol against toxicity induced by 6-hydroxydopamine and 1-methyl-4-phenylpyridinium ion (MPP+) towards dopaminergic mesencephalic neurones in primary culture [J].
Callier, S ;
Le Saux, M ;
Lhiaubet, AM ;
Di Paolo, T ;
Rostène, W ;
Pelaprat, D .
JOURNAL OF NEUROCHEMISTRY, 2002, 80 (02) :307-316
[7]   Kinetic properties of human dopamine sulfotransferase (SULT1A3) expressed in prokaryotic and eukaryotic systems:: Comparison with the recombinant enzyme purified from Escherichia coli [J].
Dajani, R ;
Sharp, S ;
Graham, S ;
Bethell, SS ;
Cooke, RM ;
Jamieson, DJ ;
Coughtrie, MWH .
PROTEIN EXPRESSION AND PURIFICATION, 1999, 16 (01) :11-18
[8]   Tryphostin AG879, a tyrosine kinase inhibitor: prevention of transcriptional activation of the electrophile and the aromatic hydrocarbon response elements [J].
Dieter, MZ ;
Freshwater, SL ;
Solis, WA ;
Nebert, DW ;
Dalton, TP .
BIOCHEMICAL PHARMACOLOGY, 2001, 61 (02) :215-225
[9]   Estrogen decreases corpus striatal neurotoxicity in response to 6-hydroxydopamine [J].
Dluzen, D .
BRAIN RESEARCH, 1997, 767 (02) :340-344
[10]  
Dluzen DE, 2002, ANN NY ACAD SCI, V965, P136