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首页> 外文期刊>Journal of environmental pathology, toxicology and oncology: official organ of the International Society for Environmental Toxicology and Cancer >Role of zinc in modulating histo-architectural and biochemical alterations during dimethylhydrazine (DMH)-induced rat colon carcinogenesis.
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Role of zinc in modulating histo-architectural and biochemical alterations during dimethylhydrazine (DMH)-induced rat colon carcinogenesis.

机译:锌在二甲基肼(DMH)诱导的大鼠结肠癌发生过程中调节组织结构和生化变化的作用。

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摘要

The aim of the present work was to gain insight into the putative anticancer effect of dietary zinc during 1,2 dimethylhydrazine (DMH)-induced colon carcinogenesis. The rats were segregated into four groups, namely, normal control, DMH-treated, zinc-treated, and (DMH + zinc)-treated. Colon carcinogenesis was induced through weekly subcutaneous injections of DMH (30 mg/kg body weight) for 12 weeks. Zinc in the form of zinc sulfate was supplemented to rats at a dose level of 227 mg/L in drinking water, ad libitum for the entire duration of the study. The effects of different treatments were studied on lipid peroxidation (LPO), reduced glutathione (GSH), and antioxidative enzymes, which included superoxide dismutase (SOD), catalase (CAT), glutathione S-transferase (GST), glutathione reductase (GR), as well as on the histoarchitecture of the colon. A total of 12 weeks of DMH treatment resulted in a significant increase in LPO. GSH levels and the activities of SOD, CAT, and GST were found to be significantly decreased following DMH treatment. A significant elevation in the activity of GR was observed following 12 weeks of DMH treatment. Histopathological studies showed well-differentiated signs of dysplasia, which included nuclei enlargement, epithelial thickening, and nuclear pleomorphism indicative of promotional phase of colon carcinogenesis in DMH-administered rats. Administration of zinc to DMH-treated rats decreased the levels of LPO and GSH significantly, but the activities of SOD and CAT were found to be significantly increased following zinc treatment. Zinc supplementation along with DMH treatment did not reveal any significant change in the activity of GR but significantly improved the activity of GST, which was depressed following DMH treatment. Also, zinc treatment in DMH-treated rats showed signs of great improvement, but structureless masses of the cells and hyperchromic nuclei were still visible occasionally. In conclusion, the results of this study suggest that zinc has a positive beneficial effect against chemically DMH-induced colonic preneoplastic progression in rats.
机译:本工作的目的是深入了解膳食锌在1,2-二甲基肼(DMH)诱导的结肠癌发生过程中的假定抗癌作用。将大鼠分为四组,即正常对照,DMH处理,锌处理和(DMH +锌)处理。通过每周皮下注射DMH(30 mg / kg体重)持续12周来诱导结肠癌发生。以227毫克/升的剂量向大鼠补充硫酸锌形式的锌,饮用水在整个研究过程中都是随意的。研究了不同处理对脂质过氧化(LPO),还原型谷胱甘肽(GSH)和抗氧化酶的影响,其中包括超氧化物歧化酶(SOD),过氧化氢酶(CAT),谷胱甘肽S-转移酶(GST),谷胱甘肽还原酶(GR) ,以及结肠的组织架构。总共12周的DMH治疗导致LPO显着增加。发现DMH处理后,GSH水平以及SOD,CAT和GST的活性显着降低。在DMH治疗12周后,观察到GR活性显着升高。组织病理学研究显示,发育异常的迹象明显不同,包括核增大,上皮增厚和核多态性,表明在DMH给药大鼠中结肠癌发生的促进阶段。向DMH处理的大鼠施用锌可显着降低LPO和GSH的水平,但发现锌处理后,SOD和CAT的活性显着增加。锌的添加以及DMH的处理并未显示GR活性有任何显着变化,但显着改善了GST的活性,DMH处理后GST的活性下降。同样,用DMH处理的大鼠中的锌处理显示出明显改善的迹象,但偶尔仍可见无结构的细胞团块和增色核。总之,这项研究的结果表明,锌对大鼠DMH化学诱导的结肠癌前发展具有积极的有益作用。

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