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Establishment of a Standardized Liver Fibrosis Model with Different Pathological Stages in Rats

机译:大鼠不同病理分期标准肝纤维化模型的建立

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摘要

Objective. To establish a standardized animal model for liver fibrosis with the same assessment criteria for liver fibrosis studies that have been established on a unified platform. Methods. The standardized liver fibrosis model was established using Sprague-Dawley (SD) rats that either received an intraperitoneal injection of carbon tetrachloride (CCl4) in small dosages or ingested an ethanol solution. Results. The definite corresponding rules among modeling of different weeks and corresponding serology indices as well as different pathological staging can be observed by modeling with small dosages and slow, individualized, and combined administrations. Conclusion. This method can be used for the standardized establishment of a liver fibrosis model in rats across 5 pathological stages, ranging from S0 to S4, with a high success rate (89.33%) and low death rate (17.3%) because of the application of multiple hypotoxic chemicals for modeling. We refer to the criteria of Histological Grading and Staging of Chronic Hepatitis for Fibrosis established by the 10th World Digestive Disease Academic Conference in Los Angeles in September 1994 (revised in November 2000).
机译:目的。建立具有统一平台上建立的肝纤维化研究评估标准的动物肝纤维化标准化动物模型。方法。使用Sprague-Dawley(SD)大鼠建立标准化的肝纤维化模型,该大鼠要么接受小剂量腹腔注射四氯化碳(CCl4),要么摄入乙醇溶液。结果。通过小剂量和缓慢,个体化和联合给药的模型,可以观察到不同星期的建模和相应的血清学指标以及不同病理分期之间的明确对应规则。结论。该方法可用于从S0到S4的5个病理阶段的大鼠肝纤维化模型的标准化建立,由于多次应用,成功率高(89.33%)和死亡率低(17.3%)用于建模的低毒化学品。我们参考的是1994年9月在洛杉矶召开的第十届世界消化系统疾病学术会议(2000年11月修订)建立的慢性肝炎纤维化的组织学分级和分期标准。

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