首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Systemic Hemodynamics and Regional Blood Flow During Chronic Nitric Oxide Synthesis Inhibition in Pregnant Rats
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Systemic Hemodynamics and Regional Blood Flow During Chronic Nitric Oxide Synthesis Inhibition in Pregnant Rats

机译:孕鼠慢性一氧化氮合成抑制过程中的全身血流动力学和局部血流量

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Pregnancy-induced hypertension in women is associated with severe vasoconstriction and reductions in organ blood flow and cardiac output. Recent studies have indicated that nitric oxide (NO) synthesis inhibition during mid to late gestation in pregnant rats results in severe hypertension and proteinuria. The purpose of this study was to determine the systemic hemodynamic and regional blood flow alterations associated with chronic NO synthesis inhibition in the pregnant rat. The study was conducted in four groups of rats: virgin rats (n=6), pregnant rats (n=10), virgin rats treated with l-NAME (n=6), and pregnant rats treated with l-NAME (n=11). Rats were treated with l-NAME in drinking water at a dose of 1 mg/d for a week starting from day 13 of gestation in pregnant rats or an equivalent time for virgins. Mean arterial pressure (MAP), cardiac output, total peripheral resistance (TPR), and regional flows were measured by tracing radiolabeled microspheres in conscious rats. Pregnant rats that were given l-NAME showed significantly higher MAP (137±6 versus 96±2 mm Hg), higher TPR (5.08±0.58 versus 2.90±0.44 mm Hg/mL/min/100 g), and lower cardiac output (87.4±8.4 versus 113.3±11.1 mL/min) than pregnant controls. Chronic NO synthesis inhibition decreased the renal blood flow in pregnant rats at a significantly greater magnitude than in virgin rats. Significant reductions in regional blood flow to the heart, lungs, liver, diaphragm, and skeletal muscles were also observed in pregnant rats treated with l-NAME. The results of this study indicate that NO may play a role in mediating the alterations in systemic hemodynamics and regional blood flow in late pregnant rats.
机译:妇女因妊娠而引起的高血压与严重的血管收缩以及器官血流量和心输出量降低有关。最近的研究表明,妊娠中晚期妊娠大鼠一氧化氮(NO)的合成抑制会导致严重的高血压和蛋白尿。这项研究的目的是确定与妊娠大鼠慢性NO合成抑制相关的全身血流动力学和区域血流变化。该研究在四组大鼠中进行:原始大鼠(n = 6),怀孕大鼠(n = 10),用l-NAME治疗的原始大鼠(n = 6)和用l-NAME治疗的怀孕大鼠(n = 6) 11)。从妊娠大鼠妊娠的第13天开始,或在同等时间处女,在饮用水中以1 mg / d的剂量在大鼠中用l-NAME处理大鼠一周。通过追踪清醒大鼠的放射性标记微球,测量平均动脉压(MAP),心输出量,总外周阻力(TPR)和区域血流。给予l-NAME的怀孕大鼠显示出明显更高的MAP(137±6比96±2 mm Hg),更高的TPR(5.08±0.58比2.90±0.44 mm Hg / mL / min / 100 g)和更低的心输出量(与孕妇对照组相比为87.4±8.4 vs.113.3±11.1 mL / min)。慢性NO合成抑制作用使怀孕大鼠的肾血流量降低的幅度明显大于处女大鼠。在用l-NAME治疗的怀孕大鼠中,还观察到流向心脏,肺,肝,diaphragm肌和骨骼肌的局部血流显着减少。这项研究的结果表明,NO可能在晚期妊娠大鼠的系统性血流动力学和局部血流的调节中发挥作用。

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