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多沙唑嗪可预防糖尿病大鼠的蛋白尿和硫酸乙酰肝素的肾小球丢失。

Doxazosin prevents proteinuria and glomerular loss of heparan sulfate in diabetic rats.

作者信息

Jyothirmayi G N, Alluru I, Reddi A S

机构信息

Department of Medicine, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark 07103, USA.

出版信息

Hypertension. 1996 May;27(5):1108-14. doi: 10.1161/01.hyp.27.5.1108.

Abstract

We examined whether blood pressure reduction or good glycemic control equally lower albuminuria by preventing glomerular loss of heparan sulfate and progression of glomerulosclerosis in streptozotocin-induced diabetic rats. We used doxazosin, and alpha 1-adrenergic blocker, to lower systemic blood pressure, and good glycemic control was achieved by insulin treatment. Rats were killed after 20 weeks of treatment. Doxazosin significantly lowered systolic pressure in diabetic rats; however, it had no effect in normal rats. Good glycemic control also lowered systolic pressure. In diabetic rats with good glycemic control, doxazosin had an additive effect on blood pressure. Glomerular heparan sulfate synthesis was significantly lower and urinary albumin excretion higher in diabetic than in normal rats. Both doxazosin treatment and good glycemic control normalized these abnormalities in diabetic rats. Insulin normalized plasma glucose and glycosylated HbA1 concentrations in diabetic rats, as did doxazosin. Significant increases in mesangial area and glomeruloscelerosis were observed in diabetic rats. Only good glycemic control normalized these pathological changes in all diabetic rats. Two-way factorial ANOVA showed an interaction between the effects of doxazosin and insulin on systolic pressure and plasma glucose. The data show that after 20 weeks of doxazosin treatment, albuminuria was reduced by 80%; however, this treatment had no significant effect on mesangial expansion or progression to glomerulosclerosis. Conversely, good glycemic control prevented all three of the preceding sequelae.

摘要

我们研究了在链脲佐菌素诱导的糖尿病大鼠中,血压降低或良好的血糖控制是否通过防止硫酸乙酰肝素的肾小球丢失和肾小球硬化的进展来同等程度地降低蛋白尿。我们使用α1肾上腺素能阻滞剂多沙唑嗪来降低全身血压,并通过胰岛素治疗实现良好的血糖控制。治疗20周后处死大鼠。多沙唑嗪显著降低糖尿病大鼠的收缩压;然而,它对正常大鼠没有影响。良好的血糖控制也能降低收缩压。在血糖控制良好的糖尿病大鼠中,多沙唑嗪对血压有相加作用。糖尿病大鼠的肾小球硫酸乙酰肝素合成显著低于正常大鼠,尿白蛋白排泄则更高。多沙唑嗪治疗和良好的血糖控制均使糖尿病大鼠的这些异常恢复正常。胰岛素使糖尿病大鼠的血浆葡萄糖和糖化血红蛋白A1浓度恢复正常,多沙唑嗪也有同样效果。在糖尿病大鼠中观察到系膜面积和肾小球硬化显著增加。只有良好的血糖控制使所有糖尿病大鼠的这些病理变化恢复正常。双向析因方差分析显示多沙唑嗪和胰岛素对收缩压和血浆葡萄糖的作用之间存在相互作用。数据表明,多沙唑嗪治疗20周后,蛋白尿减少了80%;然而,这种治疗对系膜扩张或肾小球硬化的进展没有显著影响。相反,良好的血糖控制预防了上述所有三种后遗症。

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