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An Attempt to Establish a Common Animal Model for Hepatorenal Fibrosis in Rats

机译:建立大鼠肝肾纤维化常见动物模型的尝试

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摘要

It is already a proven fact that there exists a relationship between CLD (chronic liver disease) and kidney disease but still there is no available combined animal model of liver and kidney fibrosis on the same animal. An animal model is one of the important research tools in the field of medical science because it is important to build a model that can simulate the disease condition so that the particular disease can be studied. Therefore, the aim of this study is to build a less expensive, less time consuming, and reproducible model of hepatorenal fibrosis on rats. We administered combined intraperitoneal injection of CCl4 (Carbon Tetrachloride) and BSA (Bovine Serum Albumin) on a female Wistar rats. At the end, the liver and kidney tissues were examined under microscope to see whether we were successful in establishing the model or not. The results show that liver fibrosis was marked but the changes on the kidneys were mild. In this study, we were able to induce significant fibrosis in the liver and early stages of fibrosis in the kidneys. The result also demonstrated that the addition of BSA conferred a liver protective effect against CCl4 induced hepatotoxicity, whereas combination of CCl4 and BSA proved to be detrimental for kidneys.
机译:已经被证实的事实是,CLD(慢性肝病)和肾脏疾病之间存在联系,但是在同一只动物上尚无可用的肝肾纤维化联合动物模型。动物模型是医学领域中重要的研究工具之一,因为建立可模拟疾病状况的模型以对特定疾病进行研究非常重要。因此,本研究的目的是建立大鼠肝肾纤维化的便宜,耗时和可重现的模型。我们在雌性Wistar大鼠上联合腹膜内注射CCl4(四氯化碳)和BSA(牛血清白蛋白)。最后,在显微镜下检查肝和肾组织,看我们是否成功建立了模型。结果表明,肝纤维化明显,但肾脏的变化较轻。在这项研究中,我们能够在肝脏中诱导明显的纤维化,在肾脏中诱导早期的纤维化。该结果还证明,添加BSA赋予肝脏抗CCl4诱导的肝毒性的作用,而CCl4和BSA的组合被证明对肾脏有害。

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