二乙基硝基胺和四氯化碳对褐家鼠肾组织形态的影响

Almas Dwi Khairana, R. Raissa, W. Riawan, S. Suharti, H. Susanto, Aulanni’am Aulanni’am
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引用次数: 0

摘要

二乙基亚硝胺(DEN)是各种食品和饮料的代谢产物,其中含有硝酸盐和亚硝酸盐形式的防腐剂。亚硝胺存在于各种产品中,如酒精饮料、加工肉类、香烟和化妆品。DEN对肝脏、肺、肾、皮肤、胃和血液等器官具有毒性和致癌性。除了给予DEN化合物外,还有CCl4化合物作为肿瘤启动剂,称为遗传毒性物质,可增加遗传错误的风险并刺激细胞成为恶性肿瘤。DEN和CCl4诱导可损害人体各器官,其中之一是肾脏。在健康的身体中,血管生成在伤口愈合和新组织形成中起着重要作用。然而,血管生成也有助于致癌或癌细胞的不受控制的生长,并且当身体被有毒物质污染时是恶性的。因此,为了确定DEN和CCl4给药的效果,我们采用免疫组织化学方法观察,以VEGF血管生成因子为基础,观察实验动物、阳性对照组和阴性对照组肾脏的组织学差异。从这些结果来看,存在显著差异。阴性组未见坏死及VEGF高值表达,阳性组较阴性对照组出现坏死及VEGF高值表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giving of Diethylnitrisamine and Carbon Tetrachloride on Histological Appearance of Rat Kidney (Rattus Norvegicus)
Diethylnitrosamine (DEN) is a metabolic product of various foods and beverages in which there are preservatives in the form of nitrate and nitrite. Nitrosamines are found in various products such as alcoholic beverages, processed meats, cigarettes, and cosmetic products. DEN is toxic and carcinogenic to organs such as the liver, lungs, kidneys, skin, stomach, and blood. In addition to giving DEN compounds, there are also CCl4 compounds as tumor promoter agents known as genotoxic substances that can increase the risk of genetic errors and stimulate cells to become malignant neoplasms. Administration of DEN and CCl4 induction can damage various organs of the body, one of which is the kidney. In a healthy body, angiogenesis plays a role in wound healing and the formation of new tissue. However, angiogenesis also contributes to carcinogenesis or the uncontrolled growth of cancer cells, and is malignant when the body is contaminated with toxic substances. Therefore, to determine the effect of the administration of DEN and CCl4 observations were made using the immunohistochemical method, to see differences in the histology of the kidneys of experimental animals, the positive control group, and the negative control group based on the VEGF angiogenesis factor. From these results, there are significant differences. In the negative group, there was no necrosis and high-value VEGF expression, but in the positive group, there was necrosis and a decrease in the value of VEGF expression compared to the negative control group.
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