Garini G, Mazzi A, Allegri L, Buzio C, Borghetti A
Institute of Clinical Medicine and Nephrology, University of Parma, Italy.
Miner Electrolyte Metab. 1996;22(1-3):123-7.
To determine whether the increase in proteinuria resulting from high dietary protein intake could be prevented by angiotensin-converting enzyme inhibition (ACEI), we performed paired studies on 8 nephrotic patients with normal GFR. They were fed sequential diets with a protein content of 0.8 (LPD) and 1.6 g/kg BW (HPD) each for 8 weeks. Patients on HPD received enalapril (ENAL) 10 mg/day. Despite the significant difference in protein intake, urinary protein excretion, at the end of the two dietary periods, was not statistically different. However, total serum protein and serum albumin increased significantly with HPD + ENAL treatment. The capability of ACEI to prevent the increase in proteinuria induced by HPD may be due to changes in glomerular hemodynamics, possibly mediated by changes in the activity of angiotensin II. Our study indicates that protein metabolism in nephrotic patients is better maintained with HPD + ENAL than with LPD alone.
为了确定通过血管紧张素转换酶抑制(ACEI)能否预防高膳食蛋白质摄入导致的蛋白尿增加,我们对8名肾小球滤过率(GFR)正常的肾病患者进行了配对研究。他们依次接受蛋白质含量分别为0.8(低蛋白饮食,LPD)和1.6 g/kg体重(高蛋白饮食,HPD)的饮食,各为期8周。接受HPD的患者每天服用依那普利(ENAL)10 mg。尽管蛋白质摄入量存在显著差异,但在两个饮食阶段结束时,尿蛋白排泄量并无统计学差异。然而,HPD + ENAL治疗使总血清蛋白和血清白蛋白显著增加。ACEI预防HPD诱导的蛋白尿增加的能力可能归因于肾小球血流动力学的变化,这可能由血管紧张素II活性的改变介导。我们的研究表明,与单独的LPD相比,HPD + ENAL能更好地维持肾病患者的蛋白质代谢。