Cheng E Y, Lee C, Decker R S, Sensibar J A, Lang S, Kaplan W E, Maizels M, Firlit C F
Division of Urology, Children's Memorial Hospital, Chicago IL 60614, USA.
Urology. 1997 Sep;50(3):465-71. doi: 10.1016/S0090-4295(97)00266-5.
To investigate whether angiotensin II has a role in the regulation of bladder smooth muscle growth and function, we developed a model of bladder neck obstruction (BNO) in the neonatal rabbit and investigated the effect of captopril (angiotensin converting enzyme inhibitor) on the obstructive changes in the developing bladder.
Partial BNO was induced in a group of 2-day-old rabbits (n = 8) by placing a loose 2-0 silk ligature around the vesicourethral junction. A second group of rabbits subjected to the identical partial BNO procedure (n = 8) was given captopril (1 mg/kg/day). Twelve days postobstruction, bladders from these animals, along with paired controls (n = 8), were harvested and assayed for total protein, DNA, and collagen content.
Partial BNO resulted in a 170% increase in wet weight (P < 0.05), 132% increase in protein/deoxyribonucleic acid (DNA) ratio (P < 0.05), 75% increase in total DNA (P < 0.05), and 115% increase in total collagen (P < 0.05). When compared with obstructed animals, captopril administration significantly inhibited the increase in total DNA (P < 0.05) and reduced the amount of total collagen (P = 0.054). Examination of histology specimens demonstrated that captopril inhibited the serosal hyperplasia and collagen deposition associated with obstruction.
These data demonstrate that captopril partially inhibits the changes in the neonatal rabbit bladder associated with obstruction, supporting the hypothesis that angiotensin II is involved in the regulation of bladder smooth muscle growth and collagen production.
为了研究血管紧张素II在膀胱平滑肌生长和功能调节中是否起作用,我们建立了新生兔膀胱颈梗阻(BNO)模型,并研究了卡托普利(血管紧张素转换酶抑制剂)对发育中膀胱梗阻性变化的影响。
通过在膀胱尿道交界处放置一根宽松的2-0丝线结扎,对一组2日龄兔子(n = 8)诱导部分BNO。对另一组接受相同部分BNO手术的兔子(n = 8)给予卡托普利(1 mg/kg/天)。梗阻后12天,收集这些动物的膀胱以及配对对照(n = 8)的膀胱,检测总蛋白、DNA和胶原蛋白含量。
部分BNO导致湿重增加170%(P < 0.05),蛋白质/脱氧核糖核酸(DNA)比率增加132%(P < 0.05),总DNA增加75%(P < 0.05),总胶原蛋白增加115%(P < 0.05)。与梗阻动物相比,给予卡托普利可显著抑制总DNA的增加(P < 0.05)并减少总胶原蛋白的量(P = 0.054)。组织学标本检查表明,卡托普利抑制了与梗阻相关的浆膜增生和胶原蛋白沉积。
这些数据表明,卡托普利部分抑制新生兔膀胱与梗阻相关的变化,支持血管紧张素II参与膀胱平滑肌生长和胶原蛋白产生调节的假说。