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Hyperglycemia and Renal Mass Ablation Synergistically Augment Albuminuria in the Diabetic Subtotally Nephrectomized Rat: Implications for Modeling Diabetic Nephropathy

机译:高血糖和肾脏肿块消融协同增强肾小管肾切除大鼠的白蛋白尿:对糖尿病性肾病建模的意义。

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Background/Aims: While experimental models that emulate diabetic nephropathy are valuable tools for elucidating pathogenetic mechanisms and developing novel therapies, existing models imperfectly recapitulate human disease. In diabetes, hyperglycemia and hemodynamic forces act in concert to induce renal injury. Accordingly, in the present study, we combined streptozotocin-induced diabetes with surgical ablation of 5/6 of the kidney mass with the aim of evaluating their additive effects on renal function and glomerular morphology. Methods: Female F344 rats were randomized to undergo subtotal nephrectomy (SNx) either at baseline or following 4 weeks of diabetes. Results: In comparison to sham rats, rats with diabetes or rats after SNx surgery, diabetic subtotally nephrectomized (DM-SNx) rats demonstrated an increase in systolic blood pressure, glomerular volume and mesangial matrix. Albuminuria was synergistically increased by hyperglycemia and renal mass ablation associated with decreased nephrin expression. In contrast, glomerular capillary rarefaction and glomerular filtration rate were similarly reduced in SNx and DM-SNx rats. Conclusion: The DM-SNx rat recapitulates some of the features of human disease, most notably augmented albuminuria. Since this model avoids the deletion or overexpression of gene(s) linked to the pathogenesis of nephropathy, the DM-SNx rat model represents a complementary tool for the trial of novel therapies.
机译:背景/目的:虽然模拟糖尿病性肾病的实验模型是阐明病因机制和开发新疗法的有价值的工具,但现有模型不能完美地概括人类疾病。在糖尿病中,高血糖症和血液动力共同作用导致肾损伤。因此,在本研究中,我们将链脲佐菌素诱导的糖尿病与手术切除5/5的肾脏肿块相结合,以评估其对肾功能和肾小球形态的累加作用。方法:将雌性F344大鼠在糖尿病基线或糖尿病4周后随机进行亚全肾切除术(SNx)。结果:与假手术大鼠,糖尿病大鼠或SNx手术后的大鼠相比,糖尿病性小脑肾切除术(DM-SNx)的大鼠表现出收缩压,肾小球体积和肾小球系膜基质的增加。高血糖和肾脏肿块消融与肾素表达降低相关,蛋白尿协同增加。相反,SNx和DM-SNx大鼠的肾小球毛细血管稀疏性和肾小球滤过率同样降低。结论:DM-SNx大鼠概括了人类疾病的某些特征,最明显的是白蛋白尿增多。由于该模型避免了与肾病发病机制相关的基因的缺失或过表达,因此DM-SNx大鼠模型代表了一种用于尝试新疗法的补充工具。

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