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长期接受雌二醇治疗的雄性和雌性ACI大鼠大脑中的II期抗氧化酶活性。

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

作者信息

Stakhiv Timothy M, Mesia-Vela Sonia, Kauffman Frederick C

机构信息

Laboratory for Cellular and Biochemical Toxicology, Joint Graduate Program of Toxicology, Rutgers, The State University of New Jersey and The University of Medicine and Dentistry of New Jersey, Piscataway, NJ 08854, USA.

出版信息

Brain Res. 2006 Aug 9;1104(1):80-91. doi: 10.1016/j.brainres.2006.05.093. Epub 2006 Jul 5.

Abstract

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 E(2) 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.

摘要

在长期暴露于低剂量雌二醇(E₂)的八月-哥本哈根爱尔兰(ACI)大鼠的大脑中,检测了Ⅱ相抗氧化酶的活性,这些酶包括NAD(P)H:醌氧化还原酶1(NQO1)、谷胱甘肽S-转移酶(GST)、尿苷二磷酸葡萄糖醛酸基转移酶(UGT)和酚磺基转移酶1A1(SULT1A1)。选择ACI大鼠进行研究是因为与其他品系相比,该品系对低剂量E₂治疗高度敏感,这一点可通过E₂诱导的乳腺肿瘤高发率得到体现。大鼠长期皮下植入含3 mg E₂的胆固醇丸剂,持续6周。这种处理增加了雄性而非雌性ACI大鼠纹状体中所有四种酶的活性。处死时的血E₂水平与纹状体NQO1、GST和SULT1A1的活性密切相关,但与纹状体UGT的活性无关。包括皮质、小脑和海马体在内的其他脑区的NQO1、GST和SULT1A1活性对长期E₂处理的敏感性较低。在对照和E₂处理大鼠中,NQO1主要定位于血管成分和神经元,SULT1A1主要定位于神经元和神经毡。总体而言,这些结果表明,NQO1、GST和SULT1A1表达的增强可能有助于E₂在纹状体中的抗氧化作用,纹状体是大脑中的一个区域,由于其儿茶酚胺含量高,可能特别容易受到氧化应激的影响。

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