目的观察复方肾华胶囊对改良大鼠慢性血清病肾炎模型的治疗作用。
Objective To observe the curative effects of Compound Shenhua Capsules (CSC) on modified chronic nephritis due to serum sickness in rats.
结论慢性移植物抗宿主模型类似人类狼疮性肾炎，是良好的狼疮肾炎模型。
Conlusion The mouse model of chronic GVHD, which is alike to human lupus nephritis, can be used as a good model of lupus nephritis.
免疫复合物型肾炎是一种经典的肾炎模型，其病理改变最终将导致肾小球硬化。
Immune complexes nephritis is a typical nephritis model, its pathological change finally lead to glomerular sclerosis.
方法：采用大鼠肾毒血清性肾炎模型，常规电镜制片、染色，观察肾组织超微结构的变化。
METHODS: Nephrotoxic serum nephritis model of rat was created by Clarkes method, and changes in ultrastructure of kidney were examined.
方法采用加速型肾毒血清肾炎致NS模型。
Methods A rat model of accelerated nephrotoxic serum nephritis with NS was used in this study.
目的制备狼疮肾炎小鼠模型。
其中大多数的结论直接来自于对大鼠膜性肾病（或称海曼肾炎）模型的研究，该动物模型很相似地模拟了人类该类疾病的临床和病理特征。
Most of these have come directly from studies carried out in the Heymann nephritis models of MN in rats, which closely simulate the clinical and pathologic features of the human disease.
给大鼠注射抗胸腺细胞血清（ATS）复制系膜增生性肾小球肾炎即ATS性肾炎（ATSN）模型。
The model of mesangioproliferative nephritis of rats, namely, anti- thymocyte serum nephritis (ATSN) was established by repeated injection of rabbit antiserum against rat thymocytes.
用阳离子化牛血清白蛋白复制家兔膜性肾小球肾炎的动物模型，并用中药肾炎益气液进行治疗。
The cationic bovine serum albumin (c-BSA) was used for duplicating experimental animal models of membranous glomerulonephritis and Shenyan Yiqi Decoction was used for treatment.
现对常见的肾小球肾炎的动物模型及其在新药评价中的作用进行综述。
The animal models mimicked common glomerulonephritis and their uses in new drug evaluation are reviewed in this article.
目的制作与人肾盂肾炎相似的动物模型，为临床治疗急慢性泌尿系感染性疾病打下实验基础。
Objective to made the animal model which is similar to the human pyelonephritis to strengthen the experimental basis for the therapy of acute urologic infectious disease.
病理结果显示模型鼠肝肾炎性改变，治疗组炎性改变减轻。
Pathologic results showed that liver and kidney appeared inflammation in model mice.
病理结果显示模型鼠肝肾炎性改变，治疗组炎性改变减轻。
Pathologic results showed that liver and kidney appeared inflammation in model mice.
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