Gonçalves L, Pacheco F, Santos C, Cabrita S, Beja M, Providência L A
Serviço de Cardiologia dos Hospitais da Universidade de Coimbra.
Rev Port Cardiol. 1994 May;13(5):417-22, 381.
To evaluate the efficacy of enalapril in preventing cardiac myocyte remodelling in rats with arteriovenous fistulas.
We distributed thirty males Wistar rats in 3 groups: group A (control), group B (fistula) and group C (fistula + enalapril). An end to side fistula between the femoral artery and vein was produced in the right thighs of rats from groups B and C. Oral enalapril (0.07 mg/kg/day) was given to rats from group C. After 8 weeks the rats were sacrificed and their heart removed for pathologic study.
Body weight evolution was similar in all groups. Heart weight increased in group B (1.78 +/- 0.2 g) when compared to group A (1.55 +/- 0.11 g), (p < 0.02), and was similar (p = n.s.) in groups A and C (1.58 +/- 0.13 g). Heart weight/Body weight ratio was also increased in group B (4.4 +/- 0.55 mg/g) when compared to group A (3.6 +/- 0.5 mg/g), (p < 0.01), but was similar in groups A and C (3.66 +/- 0.4 mg/g) (p = n.s.). An increase in wall thickness was detected in group B in the right ventricle (p < 0.03), septum (p < 0.01) and left ventricle (p < 0.01) when compared to groups A and C. Myocytes cytoplasm volume fraction was increased in group B, when compared with group A, in all segments studied (right ventricle p = 0.011, septum p = 0.025, and left ventricle p = 0.031). Groups A and C were similar.
Enalapril prevents the structural remodelling of cardiac myocytes in this model of volume overload induced by an arteriovenous fistula.
评估依那普利在预防动静脉瘘大鼠心肌细胞重塑方面的疗效。
将30只雄性Wistar大鼠分为3组:A组(对照组)、B组(瘘管组)和C组(瘘管+依那普利组)。在B组和C组大鼠的右大腿制作股动脉与静脉的端侧瘘。给C组大鼠口服依那普利(0.07毫克/千克/天)。8周后处死大鼠,取出心脏进行病理学研究。
所有组的体重变化相似。与A组(1.55±0.11克)相比,B组(1.78±0.2克)心脏重量增加(p<0.02),A组和C组(1.58±0.13克)相似(p=无统计学意义)。与A组(3.6±0.5毫克/克)相比,B组心脏重量/体重比也增加(4.4±0.55毫克/克)(p<0.01),但A组和C组相似(3.66±0.4毫克/克)(p=无统计学意义)。与A组和C组相比,B组右心室(p<0.03)、室间隔(p<0.01)和左心室(p<0.01)的壁厚度增加。与A组相比,B组所有研究节段的心肌细胞胞浆体积分数均增加(右心室p=0.011,室间隔p=0.025,左心室p=0.031)。A组和C组相似。
在这种动静脉瘘引起的容量超负荷模型中,依那普利可预防心肌细胞的结构重塑。