Fukuzawa Y, Watanabe Y, Inaguma D, Hotta N
Third Department of Internal Medicine, Nagoya University School of Medicine, Japan.
J Lab Clin Med. 1996 Dec;128(6):568-78. doi: 10.1016/s0022-2143(96)90129-8.
Otsuka Long-Evans Tokushima Fatty (OLETF) rats have been established as an animal model in which non-insulin-dependent diabetes mellitus develops spontaneously. We examined the renal histopathology and the urinary findings serially in OLETF rats and compared these findings with findings in age-matched Long-Evans Tokushima Otsuka (LETO) rats as a control strain. OLETF rats showed higher blood glucose levels than did LETO rats from 18 weeks of age, and hemoglobin A1c levels became higher in OLETF rats than in LETO rats from 22 weeks of age. Accompanying the development of hyperglycemia was an increase in the amount of albuminuria in OLETF rats from 18 weeks of age. The initial histopathologic change found in OLETF rats was an increase in glomerular area, and mesangial expansion started to develop from 22 weeks of age. Mesangial lesions progressed to mesangial sclerosis, and exudative lesions were found in OLETF rats from 36 weeks of age. The anionic charge of glomerular basement membrane (GBM), measured by polyethyleneimine grain density, demonstrated that the lower grain density in OLETF rats when compared with that in LETO rats became more evident with an increase in the amount of albuminuria. Therefore, the defect in the charge-selective property found in OLETF rats might be one of the causes of albuminuria. The GBM became thickened in elderly OLETF rats as compared with that in age-matched LETO rats. Disturbances in the selectivity of urinary protein, as determined by the clearance ratio of immunoglobulin G to transferrin, were found to accompany the thickening of GBM in OLETF rats. We consider that both the loss of the charge-selective property and massive albuminuria might be the causes of GBM thickening, through a clogging mechanism, and that GBM thickening might in turn produce the loss of size selectivity. Given these findings, we consider the OLETF strain of rats to be an interesting animal model for studying the relationship between diabetes and renal involvement, because the glomerular abnormalities and massive albuminuria found in OLETF rats were results of a long-term diabetic state.
大冢长- Evans 德岛肥胖(OLETF)大鼠已被确立为一种可自发发生非胰岛素依赖型糖尿病的动物模型。我们对OLETF大鼠的肾脏组织病理学和尿液检查结果进行了连续观察,并将这些结果与作为对照品系的年龄匹配的大冢长- Evans 德岛(LETO)大鼠的结果进行了比较。OLETF大鼠从18周龄起血糖水平就高于LETO大鼠,从22周龄起OLETF大鼠的糖化血红蛋白水平就高于LETO大鼠。随着高血糖的发展,OLETF大鼠从18周龄起蛋白尿的量就开始增加。在OLETF大鼠中发现的最初组织病理学变化是肾小球面积增加,系膜扩张从22周龄开始出现。系膜病变进展为系膜硬化,从36周龄起在OLETF大鼠中发现渗出性病变。通过聚乙烯亚胺颗粒密度测量的肾小球基底膜(GBM)的阴离子电荷表明,与LETO大鼠相比,OLETF大鼠中较低的颗粒密度随着蛋白尿的增加而变得更加明显。因此,在OLETF大鼠中发现的电荷选择性特性缺陷可能是蛋白尿的原因之一。与年龄匹配的LETO大鼠相比,老年OLETF大鼠的GBM增厚。通过免疫球蛋白G与转铁蛋白的清除率测定发现,OLETF大鼠中尿蛋白选择性的紊乱与GBM增厚同时出现。我们认为,电荷选择性特性的丧失和大量蛋白尿可能通过堵塞机制导致GBM增厚,而GBM增厚反过来可能导致大小选择性丧失。鉴于这些发现,我们认为OLETF大鼠品系是研究糖尿病与肾脏受累之间关系的一个有趣的动物模型,因为在OLETF大鼠中发现的肾小球异常和大量蛋白尿是长期糖尿病状态的结果。