Bolton W K, Sturgill B C
Br J Exp Pathol. 1978 Apr;59(2):167-77.
We administered bovine serum albumin (BSA) 1 or 3 mg i.v. into hyper-immune Sprague-Dawley rats weekly for up to 6 months. Animals with free circulating antibody 1 h after BSA developed mesangial deposits of IgG and C-3 without proteinuria. Rats without free antibody at 1 h developed either mesangial or mesangial and glomerular basement membrane (GBM) deposits. Rats given 3 mg BSA tended to have GBM deposits, proteinuria and undetectable antibody at 1 h. By electronmicroscopy, all rats had mesangial and subendothelial dense deposits, while those with GBM lesions had intramembranous and subepithelial deposits with foot process obliteration. Light microscopic evaluation of kidney tissue revealed only mild histological changes similar to those in age-matched control rats. The present studies demonstrate that prolonged i.v. administration of BSA into rats results in the development of a chronic non-inflammatory nephropathy. Despite certain parallels to chronic serum sickness nephropathy in rabbits, species differences appear to modify the nephropathy in rats.
我们每周一次静脉注射1毫克或3毫克牛血清白蛋白(BSA)至超免疫斯普拉格-道利大鼠体内,持续长达6个月。注射BSA后1小时有游离循环抗体的动物出现IgG和C-3的系膜沉积物,但无蛋白尿。1小时时无游离抗体的大鼠出现系膜或系膜及肾小球基底膜(GBM)沉积物。给予3毫克BSA的大鼠在1小时时倾向于出现GBM沉积物、蛋白尿且抗体检测不到。通过电子显微镜检查,所有大鼠均有系膜和内皮下致密沉积物,而有GBM病变的大鼠有膜内和上皮下沉积物,足突消失。肾脏组织的光镜评估仅显示出与年龄匹配的对照大鼠相似的轻度组织学变化。目前的研究表明,对大鼠长期静脉注射BSA会导致慢性非炎性肾病的发生。尽管与兔慢性血清病肾病有某些相似之处,但物种差异似乎改变了大鼠的肾病情况。