Nicholas Susanne B, Mauer Michael, Basgen John M, Aguiniga Elsa, Chon Yun
Department of Medicine, Division of Nephrology and Endocrinology, David Geffen School of Medicine at UCLA, Los Angeles, Calif., USA.
Am J Nephrol. 2004 Sep-Oct;24(5):549-56. doi: 10.1159/000082001. Epub 2004 Nov 10.
BACKGROUND/AIMS: The streptozotocin (STZ)-induced diabetic rat is a widely used animal model of human diabetic nephropathy. In this model, diabetic nephropathy progresses without significant elevation in blood pressure. Therefore, studies have examined the effect of hypertension in STZ spontaneously hypertensive rats (SHR). This study investigated angiotensin II (Ang II)-induced hypertension in diabetic nephropathy in the STZ-diabetic rat independent of deleterious genetic effects in SHR.
Animals were divided as follows: nondiabetic controls (ND; n = 18); diabetic (STZ: 65 mg/kg; n = 16); Ang II-induced hypertensive ND (Ang II: 120 ng/kg/min; n = 9), and hypertensive diabetic rats (n = 18). Systolic blood pressure was measured by the tail-cuff method prior to STZ injection and then weekly. After 3 months, plasma creatinine, and 24-hour urine albumin and creatinine were measured and kidneys harvested for morphometry.
Ang II infusion increased systolic blood pressure in diabetic and ND rats. When combined with diabetes, Ang II increased albumin excretion rate (14-fold, p < 0.05), plasma creatinine (1.5-fold, p < 0.005) worsened creatinine clearance (37%, p < 0.002) and increased glomerular basement membrane width (1.2-fold, p < 0.0001).
Ang II caused moderate hypertension and accelerated diabetic nephropathy and glomerular structural changes. The Ang II-infused STZ-diabetic rat is an excellent model to study the deleterious glomerular effects of hypertension on diabetes independent of genetic traits.
背景/目的:链脲佐菌素(STZ)诱导的糖尿病大鼠是一种广泛应用于人类糖尿病肾病的动物模型。在该模型中,糖尿病肾病进展时血压无显著升高。因此,已有研究探讨高血压在STZ自发性高血压大鼠(SHR)中的作用。本研究调查了在STZ糖尿病大鼠中,血管紧张素II(Ang II)诱导的高血压对糖尿病肾病的影响,而不受SHR中有害遗传效应的影响。
动物分为以下几组:非糖尿病对照组(ND;n = 18);糖尿病组(STZ:65 mg/kg;n = 16);Ang II诱导的高血压ND组(Ang II:120 ng/kg/min;n = 9),以及高血压糖尿病大鼠组(n = 18)。在注射STZ前通过尾套法测量收缩压,之后每周测量一次。3个月后,测量血浆肌酐、24小时尿白蛋白和肌酐,并摘取肾脏进行形态学测量。
输注Ang II可使糖尿病和ND大鼠的收缩压升高。与糖尿病合并时,Ang II可使白蛋白排泄率增加(14倍,p < 0.05),血浆肌酐增加(1.5倍,p < 0.005),肌酐清除率恶化(37%,p < 0.002),并增加肾小球基底膜宽度(1.2倍,p < 0.0001)。
Ang II导致中度高血压,并加速糖尿病肾病和肾小球结构改变。输注Ang II的STZ糖尿病大鼠是研究高血压对糖尿病的有害肾小球效应且不受遗传特征影响的理想模型。