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在结肠癌发生过程中,喂食高铁水平饲料的大鼠体内锰超氧化物歧化酶活性降低。

Decrease of manganese superoxide dismutase activity in rats fed high levels of iron during colon carcinogenesis.

作者信息

Kuratko C N

机构信息

Department of Pathology, Texas Tech Health Sciences Center, Lubbock 79430, USA.

出版信息

Food Chem Toxicol. 1998 Sep-Oct;36(9-10):819-24. doi: 10.1016/s0278-6915(98)00029-5.

Abstract

Diets high in fat or iron have been associated with an increased risk for development of colon cancer. These two dietary factors are known to decrease manganese superoxide dismutase (MnSOD) activity in colonic mucosa. MnSOD is an antioxidant enzyme that protects mitochondria from oxygen radical damage. MnSOD has tumour suppressive activity and is absent or decreased in most tumours, including those from the colon. This study was designed to determine the effects of high dietary lipid and iron levels on MnSOD activity during the early weeks of colon carcinogenesis. Male Fischer-344 rats were fed 20% lipid diets of either corn oil or menhaden oil containing adequate iron (35 mg/kg) or supplemental iron (535 mg/kg). Rats from each diet were divided into carcinogen treatment groups and given two weekly injections of either azoxymethane (AOM) at a dose of 12 mg/kg, or saline. Mucosal tissue was collected 1, 6 and 12 wk following injections and analysed for MnSOD activity, mineral concentration and nuclear aberrations. Results showed that iron supplementation increased nuclear aberrations, and decreased manganese concentration and MnSOD activity in colonic mucosa ot control animals. AOM, and interaction of iron and AOM, also decreased MnSOD activity. A decrease in the activity of this enzyme during carcinogenesis may be one mechanism whereby these dietary factors ultimately increase tumour risk.

摘要

高脂肪或高铁饮食与结肠癌发生风险增加有关。已知这两种饮食因素会降低结肠黏膜中锰超氧化物歧化酶(MnSOD)的活性。MnSOD是一种抗氧化酶,可保护线粒体免受氧自由基损伤。MnSOD具有肿瘤抑制活性,在大多数肿瘤(包括结肠癌肿瘤)中不存在或减少。本研究旨在确定在结肠癌发生早期,高膳食脂质和铁水平对MnSOD活性的影响。给雄性Fischer-344大鼠喂食含适量铁(35毫克/千克)或补充铁(535毫克/千克)的20%玉米油或鲱鱼油脂质饮食。每种饮食的大鼠被分为致癌物处理组,每周注射两次剂量为12毫克/千克的偶氮甲烷(AOM)或生理盐水。在注射后1、6和12周收集黏膜组织,分析MnSOD活性、矿物质浓度和核畸变。结果表明,补充铁会增加对照动物结肠黏膜中的核畸变,并降低锰浓度和MnSOD活性。AOM以及铁与AOM的相互作用也会降低MnSOD活性。在致癌过程中这种酶活性降低可能是这些饮食因素最终增加肿瘤风险的一种机制。

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