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Effect of Insulin Therapy on Renal Changes in Spontaneously Diabetic Torii Rats

机译:胰岛素治疗对糖尿病大鼠自发性肾脏变化的影响

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The spontaneously diabetic Torii (SDT) rat has recently been established as an animal model of non-obese type 2 diabetes, in which ocular complications severe occur. However, the function and morphological features of the diabetic renal lesions in SDT rats have not been reported in detail. Therefore, we evaluated changes over time in renal lesions in SDT rats. In addition, SDT rats were treated with insulin to observe whether these renal complications are caused by hyperglycemia. Renal functional parameters and renal lesions were monitored in SDT rats from 8 to 68 weeks of age. Sprague-Dawley (SD) rats of similar age were used as control animals. In the insulin-treated group of SDT rats, insulin pellets were implanted at 24 weeks of age to compare the development of renal lesions. The SDT rats began to develop hyperglycemia at 20 weeks of age. In the histopathological examination of the kidney, glycogen deposition of the renal tubular epithelium and renal tubular dilation were observed from 24 weeks of age in the untreated SDT rats, and the changes in the renal tubules markedly progressed with aging. Moreover, thickening of the glomerular basement membrane was observed from 32 weeks of age. At 50 weeks of age, the glomeruli showed increase of mesangial matrix, with predominantly diffuse lesions showing by 68 weeks of age. The mesangial proliferation gradually progressed. In the SD rats, no renal lesions were present at 50 and 68 weeks of age. SDT rats with insulin treatment remained normoglycemic throughout observation and their renal functional parameters were normal. Glycemic control in SDT rats prevented the development of renal lesions. The features of SDT rats indicate their usefulness as an animal model for investigating diabetic nephropathy.
机译:自发性糖尿病性Torii(SDT)大鼠最近已被建立为非肥胖2型糖尿病的动物模型,其中严重发生眼部并发症。然而,尚无关于SDT大鼠糖尿病性肾脏病变的功能和形态特征的详细报道。因此,我们评估了SDT大鼠肾脏病变随时间的变化。此外,对SDT大鼠进行胰岛素治疗,以观察这些肾脏并发症是否由高血糖症引起。在8至68周龄的SDT大鼠中监测肾功能参数和肾损害。将相似年龄的Sprague-Dawley(SD)大鼠用作对照动物。在经胰岛素治疗的SDT大鼠组中,在24周龄时植入了胰岛素颗粒,以比较肾脏病变的发展。 SDT大鼠在20周龄时开始出现高血糖症。在肾脏的组织病理学检查中,未治疗的SDT大鼠从24周龄开始观察到肾小管上皮的糖原沉积和肾小管扩张,并且随着年龄的增长,肾小管的变化明显进展。此外,从32周龄开始观察到肾小球基底膜增厚。在50周龄时,肾小球显示出肾小球系膜基质增加,到68周龄时,主要表现为弥漫性病变。系膜增生逐渐进行。在SD大鼠中,在50和68周龄时没有肾脏损伤。在整个观察期间,接受胰岛素治疗的SDT大鼠均保持血糖正常,并且其肾功能参数正常。 SDT大鼠的血糖控制阻止了肾脏病变的发展。 SDT大鼠的特征表明它们作为研究糖尿病性肾病的动物模型的有用性。

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