Bertani T, Zoja C, Abbate M, Rossini M, Remuzzi G
Mario Negri Institute for Pharmacological Research, Bergamo, Italy.
Lab Invest. 1989 Feb;60(2):196-204.
Tubulointerstitial damage and glomerular sclerosis are findings commonly observed in the experimental models of adriamycin and puromycin aminonucleoside nephrosis. It has been suggested that in such models proteinuria might be an important mediator of tubulo-interstitial damage which in turn may determine the progression of the disease favoring the development of glomerulosclerosis. The objective of the present investigation was to establish the temporal relationship between proteinuria, tubulo-interstitial damage and glomerulosclerosis in aging rats with intact kidneys exposed to diets with different protein content. There were six groups of rats studied. Animals of groups 1, 5, and 6 (N = 10) were fed diets containing 20, 35, and 6% protein, respectively, for 20 months and sacrificed at the end of the experimental period. Rats in groups 3 and 4 (N = 6) exhibited marked and mild proteinuria, respectively, after 14 months of maintenance on standard diet, and followed for two additional months after the onset of proteinuria with the aim of evaluating the pattern of renal damage after a relatively short period of proteinuria. Rats in group 2 (N = 10) were fed standard diet and sacrificed before (5 months) and at the onset of proteinuria (10 months). Protein excretion and plasma creatinine were measured for each animal every month. Pathologic examination was performed by light and electron microscopy. At the onset of proteinuria neither renal structural nor functional abnormalities were detected. After 20 months, rats fed standard diet developed tubulo-interstitial damage (score: 1.29 +/- 1.05) and focal glomerular sclerosis (percentage of glomeruli with focal segmental glomerular sclerosis: 16.70 +/- 16.40). A significant correlation was found between the degree of tubulo-interstitial damage and the percentage of glomeruli with focal glomerular sclerosis (r = 0.99, p less than 0.01). Development of tubulo-interstitial damage and focal glomerular sclerosis were correlated with heavy and sustained proteinuria. The high protein diet significantly worsened proteinuria (at month 20: 247.08 +/- 101.73 mg/day), tubulo-interstitial changes (score: 1.99 +/- 0.70), focal glomerular sclerosis (percentage of glomeruli with focal segmental glomerular sclerosis: 21.50 +/- 9.44) and was associated with deteriorating renal function (at month 20, plasma creatinine: 1.20 +/- 0.50 mg/dl).(ABSTRACT TRUNCATED AT 400 WORDS)
肾小管间质损伤和肾小球硬化是阿霉素和嘌呤霉素氨基核苷肾病实验模型中常见的表现。有人提出,在这类模型中,蛋白尿可能是肾小管间质损伤的重要介质,而肾小管间质损伤反过来可能决定疾病的进展,促进肾小球硬化的发展。本研究的目的是确定在摄入不同蛋白质含量饮食的老龄大鼠中,蛋白尿、肾小管间质损伤和肾小球硬化之间的时间关系。共研究了六组大鼠。第1、5和6组(每组n = 10)的动物分别喂食含20%、35%和6%蛋白质的饮食20个月,并在实验期结束时处死。第3和4组(每组n = 6)的大鼠在标准饮食维持14个月后分别出现明显和轻度蛋白尿,在蛋白尿出现后再随访两个月,目的是评估相对短时间蛋白尿后的肾损伤模式。第2组(每组n = 10)的大鼠喂食标准饮食,并在蛋白尿出现前(5个月)和蛋白尿出现时(10个月)处死。每月测量每只动物的蛋白质排泄量和血浆肌酐。通过光镜和电镜进行病理检查。在蛋白尿出现时,未检测到肾脏结构和功能异常。20个月后,喂食标准饮食的大鼠出现肾小管间质损伤(评分:1.29±1.05)和局灶性肾小球硬化(局灶节段性肾小球硬化的肾小球百分比:16.70±16.40)。发现肾小管间质损伤程度与局灶性肾小球硬化的肾小球百分比之间存在显著相关性(r = 0.99,p<0.01)。肾小管间质损伤和局灶性肾小球硬化的发展与重度和持续性蛋白尿相关。高蛋白饮食显著加重蛋白尿(20个月时:247.08±101.73mg/天)、肾小管间质变化(评分:1.99±0.70)、局灶性肾小球硬化(局灶节段性肾小球硬化的肾小球百分比:21.50±9.44),并与肾功能恶化相关(20个月时,血浆肌酐:1.20±0.50mg/dl)。(摘要截断于400字)