Department of Obstetrics and Gynecology, American University of Beirut-Medical Center, Beirut, Lebanon.
Am J Perinatol. 2012 Jun;29(6):429-34. doi: 10.1055/s-0032-1304823. Epub 2012 Mar 7.
To assess the effect of sildenafil citrate in a rat model of Nω-nitro-l-arginine methyl ester (L-NAME)-induced intrauterine growth restriction (IUGR).
An in vivo experimental study was conducted where 40 pregnant Sprague-Dawley rats were randomly assigned to receive either: (1) control, (2) L-NAME 50 mg/kg/d by gavage (days 14 to 19), (3) L-NAME and sildenafil 15 mg/kg/d by gavage, or (4) sildenafil (days 14 to 21). On day 21, a hysterotomy was performed and all fetuses (live and dead) were counted, examined, and weighed. The primary outcome measure was the difference in pup birth weight.
The median number of live pups per dam was 11.5 (range: 1 to 15), 13.5 (2 to 17), 13.5 (7 to 16), and 11.5 (4 to 17) in controls, L-NAME, sildenafil, and combined drug groups, respectively (p = 0.02). Rats treated with L-NAME had a significantly higher number of stillbirths compared with control (p = 0.013) and sildenafil (p = 0.008) groups. L-NAME reduced pup birth weight compared with controls (4.53 ± 1.49 versus 5.65 ± 1.63 g, p < 0.001); this effect was more pronounced in the L-NAME and sildenafil groups (3.37 ± 1.25 g, p < 0.001).
Our data indicate that sildenafil citrate does not ameliorate L-NAME-induced IUGR, and in the doses utilized in this study might even have a synergistic negative effect on pup birth weight.
评估枸橼酸西地那非在 Nω-硝基-L-精氨酸甲酯(L-NAME)诱导的宫内生长受限(IUGR)大鼠模型中的作用。
进行了一项体内实验研究,将 40 只怀孕的 Sprague-Dawley 大鼠随机分为以下 4 组:(1)对照组;(2)L-NAME 50mg/kg/d 灌胃(第 14 至 19 天);(3)L-NAME 和西地那非 15mg/kg/d 灌胃;(4)西地那非(第 14 至 21 天)。第 21 天,行剖宫产术,计数、检查并称重所有活胎(死胎和活胎)。主要结局指标为仔鼠出生体重的差异。
每只母鼠的活仔鼠中位数分别为 11.5(范围:1 至 15)、13.5(2 至 17)、13.5(7 至 16)和 11.5(4 至 17),分别为对照组、L-NAME 组、西地那非组和联合用药组(p=0.02)。与对照组(p=0.013)和西地那非组(p=0.008)相比,L-NAME 组死胎数量明显更多。与对照组相比,L-NAME 降低了仔鼠出生体重(4.53±1.49 与 5.65±1.63g,p<0.001);在 L-NAME 和西地那非组中,这种作用更为明显(3.37±1.25g,p<0.001)。
我们的数据表明,枸橼酸西地那非不能改善 L-NAME 诱导的 IUGR,并且在本研究中使用的剂量下,甚至可能对仔鼠出生体重产生协同的负面影响。