Department of Cardiovascular Medicine, Institute of Health Biosciences, University of Tokushima Graduate School, Tokushima, Japan.
Hypertens Res. 2012 Nov;35(11):1058-62. doi: 10.1038/hr.2012.96. Epub 2012 Jul 5.
Cilnidipine, an L/N-type calcium channel blocker (CCB), has been reported to have more beneficial effects on proteinuria progression in hypertensive patients than amlodipine, an L-type CCB. The N-type calcium channel blockade that inhibits renal sympathetic nerve activity might reduce glomerular hypertension by facilitating vasodilation of the efferent arterioles. However, the precise mechanism of the renoprotective effect of cilnidipine remains unknown. Because cilnidipine exerted significantly higher antioxidant activity than amlodipine in cultured human mesangial cells, we hypothesized that cilnidipine might exert a renoprotective effect by suppressing oxidative stress. A total of 35 hypertensive patients receiving a renin-angiotensin system inhibitor were randomly assigned to a cilnidipine (n=18; 10 mg per day cilnidipine titrated to 20 mg per day) or amlodipine (n=17; 5 mg per day amlodipine titrated to 10 mg per day) group; the target blood pressure (BP) was set at 130/85 mmHg. After 6 months of treatment, systolic and diastolic BPs were significantly reduced in both of the groups, without any significant difference between the groups. The urinary albumin, 8-hydroxy-2'-deoxyguanosine (OHdG) and liver-type fatty-acid-binding protein (L-FABP) to creatinine ratios significantly decreased in the cilnidipine group (P<0.05) compared with those in the amlodipine group. The reductions in urinary albumin, 8-OHdG and L-FABP were not correlated with the change in systolic BP. In conclusion, cilnidipine, but not amlodipine, ameliorated urinary albumin excretion and decreased urinary 8-OHdG and L-FABP in the hypertensive patients. Cilnidipine probably exerts a greater renoprotective effect through its antioxidative properties.
西尼地平,一种 L/N 型钙通道阻滞剂(CCB),已被报道在高血压患者中比氨氯地平(一种 L 型 CCB)更能有效减缓蛋白尿的进展。N 型钙通道阻断可抑制肾交感神经活性,通过促进出球小动脉的血管舒张来降低肾小球高血压。然而,西尼地平的肾保护作用的确切机制尚不清楚。因为在培养的人肾小球系膜细胞中,西尼地平比氨氯地平表现出更高的抗氧化活性,所以我们假设西尼地平可能通过抑制氧化应激发挥肾保护作用。共有 35 名接受肾素-血管紧张素系统抑制剂治疗的高血压患者被随机分为西尼地平组(n=18;每天 10 毫克西尼地平滴定至每天 20 毫克)或氨氯地平组(n=17;每天 5 毫克氨氯地平滴定至每天 10 毫克);目标血压(BP)设定为 130/85mmHg。经过 6 个月的治疗,两组患者的收缩压和舒张压均显著降低,两组之间无显著差异。与氨氯地平组相比,西尼地平组的尿白蛋白、8-羟基-2'-脱氧鸟苷(8-OHdG)和肝型脂肪酸结合蛋白(L-FABP)与肌酐的比值显著降低(P<0.05)。西尼地平组尿白蛋白、8-OHdG 和 L-FABP 的降低与收缩压的变化无关。综上所述,西尼地平可改善高血压患者的尿白蛋白排泄,并降低尿 8-OHdG 和 L-FABP,而氨氯地平则没有这种作用。西尼地平可能通过其抗氧化特性发挥更大的肾保护作用。