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外周性高血压与肺血管调节异常。

Peripheral hypertension and alterations in pulmonary vascular regulation.

作者信息

Burke-Wolin T, Pino P, Itani M, Talerico M, Pucci M, Benson D, Fayngersh R

机构信息

Department of Pharmacology, New York Medical College, Valhalla 10595, USA.

出版信息

Am J Physiol. 1997 Jul;273(1 Pt 1):L113-8. doi: 10.1152/ajplung.1997.273.1.L113.

DOI:10.1152/ajplung.1997.273.1.L113
PMID:9252547
Abstract

We have recently reported in normal isolated-perfused rat lungs that low basal tone appears to be regulated by nitric oxide (NO)-dependent and -independent mechanisms of soluble guanylate cyclase activation. In this study, we examined the role of NO in the regulation of pulmonary artery (PA) tone from rats with renin-dependent hypertension. Rats were made hypertensive by ligating the abdominal aorta above the left and below the right renal artery (aortic coarctation, AC). Mean arterial pressure significantly increased from 119 +/- 8.4 mmHg in control animals to 156 +/- 15 mmHg 7-14 days after AC surgery. PA pressures, however, remained unchanged (8.5 +/- 3.4 mmHg in control animals vs. 11 +/- 3.3 mmHg in AC animals). Hypoxic contractions in U-46619 precontracted isolated small PA (160-260 microns diameter) were significantly increased from 51 +/- 13 mg in the control group to 142 +/- 38 mg (P < or = 0.05) in AC animals. Nitro-L-arginine (NLA; 100 microM) contractions were also enhanced in the AC animal. The enhanced NLA response may correlate with an increase in endothelial cell NO synthase (NOS) as detected by Western blotting (132 +/- 28% of control; P < 0.05). These data suggest that, in this renin-dependent model of systemic hypertension, there is increased endothelial cell NOS activity that maintains low PA tone, preventing the lung from developing increased pressures.

摘要

我们最近报道,在正常的离体灌注大鼠肺中,低基础张力似乎受一氧化氮(NO)依赖性和非依赖性可溶性鸟苷酸环化酶激活机制的调节。在本研究中,我们研究了NO在肾素依赖性高血压大鼠肺动脉(PA)张力调节中的作用。通过结扎左肾动脉上方和右肾动脉下方的腹主动脉(主动脉缩窄,AC)使大鼠患高血压。平均动脉压从对照动物的119±8.4 mmHg显著升高至AC手术后7 - 14天的156±15 mmHg。然而,PA压力保持不变(对照动物为8.5±3.4 mmHg,AC动物为11±3.3 mmHg)。在U - 46619预收缩的离体小PA(直径160 - 260微米)中,缺氧收缩从对照组的51±13毫克显著增加至AC动物的142±38毫克(P≤0.05)。AC动物中硝基 - L - 精氨酸(NLA;100 microM)引起的收缩也增强。如通过蛋白质印迹法检测到的,增强的NLA反应可能与内皮细胞一氧化氮合酶(NOS)增加有关(为对照的132±28%;P < 0.05)。这些数据表明,在这种肾素依赖性全身性高血压模型中,内皮细胞NOS活性增加,维持低PA张力,防止肺压力升高。

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