Camilión de Hurtado María C, Portiansky Enrique L, Pérez Néstor G, Rebolledo Oscar R, Cingolani Horacio E
Centro de Investigaciones Cardiovasculares, Facultad de Ciencias Médicas, Facultad de Ciencias Veterinarias, Universidad Nacional de La Plata, 60 y 120 (1900) La Plata, Argentina.
Cardiovasc Res. 2002 Mar;53(4):862-8. doi: 10.1016/s0008-6363(01)00544-2.
Experiments were performed to examine the effect of chronic inhibition of the Na(+)/H(+) exchanger isoform-1 (NHE-1) on cardiac hypertrophy of spontaneously hypertensive rats (SHR).
SHR were orally treated during 1 month with two different doses (0.3 and 3.0 mg/kg/day) of the NHE-1 inhibitor, cariporide, or nifedipine (10.0 mg/kg/day).
The two doses of cariporide did not differ in their effects after 1 month of treatment, since both induced a slight decrease in systolic blood pressure (SBP) of approximately 6 mmHg and regression of the heart weight to body weight ratio (mg/g) from 3.28+/-0.05 to 3.04+/-0.05 (0.3 mg) and 2.99+/-0.10 (3.0 mg, P<0.05). Nifedipine, given for the same period, produced similar reduction in the hypertrophy index (3.03+/-0.05), but with a much greater decrease in arterial pressure (35.6+/-7.4 mmHg). Chronic treatment with cariporide induced a complete regression of the augmented cross sectional area of left ventricular myocytes without significant changes in collagen content, serum procollagen 1 propeptide levels or myocardial distensibility.
NHE inhibition represents a novel approach to induce regression of pathological hypertrophy of the heart. The finding can be rationalized mechanistically by previous in vitro studies suggesting a role of the NHE in the development of myocardial hypertrophy.
进行实验以研究长期抑制钠氢交换体1型(NHE-1)对自发性高血压大鼠(SHR)心脏肥大的影响。
将两种不同剂量(0.3和3.0毫克/千克/天)的NHE-1抑制剂卡里波罗或硝苯地平(10.0毫克/千克/天)口服给予SHR 1个月。
治疗1个月后,两种剂量的卡里波罗效果无差异,因为二者均使收缩压(SBP)轻微下降约6毫米汞柱,并使心脏重量与体重比(毫克/克)从3.28±0.05降至3.04±0.05(0.3毫克组)和2.99±0.10(3.0毫克组,P<0.05)。同期给予硝苯地平,肥大指数有类似降低(3.03±0.05),但动脉压下降幅度更大(35.6±7.4毫米汞柱)。长期用卡里波罗治疗可使左心室心肌细胞增大的横截面积完全恢复正常,而胶原含量、血清前胶原1前肽水平或心肌伸展性无显著变化。
抑制NHE代表了一种诱导心脏病理性肥大消退的新方法。这一发现可通过先前的体外研究从机制上得到合理解释,这些研究表明NHE在心肌肥大发展中起作用。