Alexander Barbara T
Department of Physiology and Biophysics, University of Mississippi Medical Center, 2500 N State St, Jackson, MS 39216-4505, USA.
Hypertension. 2003 Mar;41(3):457-62. doi: 10.1161/01.HYP.0000053448.95913.3D. Epub 2003 Feb 3.
Low birth weight is a suggested risk factor for the development of hypertension. The purpose of the present study was to determine whether a model of intrauterine growth restriction produced in response to placental insufficiency in the pregnant rat was associated with marked elevations in blood pressure. Reduced uterine perfusion initiated in late gestation resulted in low-birth-weight offspring (5.8+/-0.1 versus 6.6+/-0.2 g, P<0.05, growth-restricted versus control, respectively). Mean arterial pressure, as measured in conscious, chronically instrumented rats, was significantly elevated as early as 4 weeks of age (113+/-3 versus 98+/-2 mm Hg, P<0.05) and was associated with significant decreases in body weight (66+/-2 versus 81+/-3 g, P<0.05) in growth-restricted (n=15) versus control (n=15) rats. Marked elevations in arterial pressure at 8 weeks of age (male: 133+/-3 versus 121+/-6 mm Hg, P<0.05; female: 137+/-4 versus 112+/-6 mm Hg, P<0.01) were associated with sex-specific decreases in body weight (male: 251+/-6 versus 275+/-10 g, P<0.05; female: 163+/-6 versus 180+/-6 g) in male growth-restricted (n=12) versus male control (n=9) rats and in female growth-restricted (n=8) versus female control (n=7) rats. At 12 weeks of age, hypertensive (144+/-4 versus 131+/-3 mm Hg, P<0.05) male growth-restricted offspring (n=10) had no alterations in glomerular filtration rate (2.3+/-0.3 versus 2.2+/-0.2 mL/min) compared with control (n=10) offspring; even when adjusted for kidney weight (1.7+/-0.3 versus 1.5+/-0.3 mL x min(-1) x g(-1) kidney), despite marked decreases in body weight (305+/-9 versus 343+/-10 g, P<0.05). These data suggest that placental insufficiency induced by reduced uterine perfusion in the pregnant rat results in low-birth-weight offspring predisposed to development of hypertension.
低出生体重被认为是高血压发生的一个风险因素。本研究的目的是确定妊娠大鼠因胎盘功能不全而产生的子宫内生长受限模型是否与血压显著升高有关。妊娠晚期开始的子宫灌注减少导致低出生体重后代(分别为5.8±0.1克和6.6±0.2克,P<0.05,生长受限组与对照组相比)。在清醒的、长期植入仪器的大鼠中测量的平均动脉压,早在4周龄时就显著升高(113±3与98±2毫米汞柱,P<0.05),并且与生长受限组(n=15)与对照组(n=15)大鼠的体重显著下降有关(66±2与81±3克,P<0.05)。8周龄时动脉压显著升高(雄性:133±3与121±6毫米汞柱,P<0.05;雌性:137±4与112±6毫米汞柱,P<0.01),与雄性生长受限组(n=12)与雄性对照组(n=9)大鼠以及雌性生长受限组(n=8)与雌性对照组(n=7)大鼠的性别特异性体重下降有关(雄性:251±6与275±10克,P<0.05;雌性:163±6与180±6克)。在12周龄时,高血压的(144±4与131±3毫米汞柱,P<0.05)雄性生长受限后代(n=10)与对照后代(n=10)相比,肾小球滤过率没有改变(2.3±0.3与2.2±0.2毫升/分钟);即使根据肾脏重量进行调整(1.7±0.3与1.5±0.3毫升×分钟-1×克-1肾脏),尽管体重显著下降(305±9与343±10克,P<0.05)。这些数据表明,妊娠大鼠子宫灌注减少引起的胎盘功能不全会导致低出生体重后代易患高血压。