Diamond J R, Karnovsky M J
Am J Pathol. 1986 Mar;122(3):481-7.
Focal and segmental glomerulosclerosis (FSGS) represents a final pathologic pattern of a number of human renal disorders. Among laboratory models, repeated intraperitoneal injections of the aminonucleoside of puromycin (PA) produces a histologic pattern not unlike the human process. A single intravenous dose of this drug usually results in glomerular morphologic changes in rats resembling those in human nephrotic syndrome with minimal changes. This report describes acute and chronic glomerular injury that begins as early as 8 days after a single central administration of PA and progresses to FSGS within an 18-week period. It seems likely that minimal change disease and FSGS are two pathologic processes in the same continuum of disease. In this model, the severity and persistence of the glomerular lesion may represent irreversible glomerular epithelial cell (GEC) injury secondary to the toxic effects of PA.
局灶节段性肾小球硬化(FSGS)是多种人类肾脏疾病的最终病理模式。在实验室模型中,反复腹腔注射嘌呤霉素氨基核苷(PA)会产生一种与人类疾病过程相似的组织学模式。单次静脉注射这种药物通常会导致大鼠肾小球形态学改变,类似于人类微小病变型肾病综合征。本报告描述了急性和慢性肾小球损伤,这种损伤最早在单次中心给予PA后8天开始,并在18周内进展为FSGS。微小病变型肾病和FSGS似乎是同一疾病连续体中的两个病理过程。在这个模型中,肾小球病变的严重程度和持续性可能代表了PA毒性作用继发的不可逆肾小球上皮细胞(GEC)损伤。