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首页> 外文期刊>American Journal of Physiology >Novel catheterization technique for the in vivo measurement of pulmonary vascular responses in rats.
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Novel catheterization technique for the in vivo measurement of pulmonary vascular responses in rats.

机译:用于体内测量大鼠肺血管反应的新型导管技术。

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A novel cardiac catheterization technique was devised to investigate the pulmonary arterial pressure-blood flow relationship in intact spontaneously breathing rats (ISBR) under physiological conditions with constant left atrial pressure and controlled blood flow within the normal range. Observations using this new technique in vivo were contrasted with data derived with isolated perfused rat lungs in vitro. Unlike results in in vitro isolated perfused rat lungs, the pressure-flow curves in vivo were curvilinear, with pulmonary artery pressure increasing more rapidly at low pulmonary blood flows of 4-8 ml/min and less rapidly at higher flow rates. Pressure-flow curves were reproducible and were not altered by 1-1.5 h of arrested perfusion, cyclooxygenase blockade, or perfusion with aortic or mixed venous blood. In contrast to results in in vitro isolated perfused rat lungs, NG-nitro-L-arginine methyl ester (L-NAME) increased pulmonary arterial pressure at all but the lowest flow rates with a slight effect on the curvilinear pressure-flow relationship. L-NAME reversed pulmonary vasodilator responses to acetylcholine and bradykinin and enhanced the pulmonary vasodilator response to nitroglycerin. The present data suggest that actively induced pulmonary hypertension is under greater control by endothelium-derived relaxing factor (EDRF). Unlike previous results in in vitro perfused rat lungs, results in ISBR demonstrate that the pulmonary vasodilator response to adrenomedullin-(13-52) is not mediated by calcitonin gene-related peptide receptors, which are not coupled to the release of EDRF. These results indicate that this novel technique may provide a useful model for the study of the pulmonary circulation in the intact chest rat.
机译:设计了一种新颖的心脏导管检查技术,以研究在生理条件下,具有恒定左心房压力并将血流量控制在正常范围内的情况下,完整自发呼吸大鼠(ISBR)的肺动脉血压与血流的关系。在体内使用这项新技术的观察结果与在体外分离出的大鼠灌注肺的数据形成对比。与体外分离的灌注大鼠肺的结果不同,体内的压力-流量曲线是曲线的,在4-8 ml / min的低肺血流量下,肺动脉压力的增加更快,而在较高的流速下,肺动脉的压力增加得较慢。压力-流量曲线是可重现的,在1-1.5 h的停滞性灌注,环氧合酶阻断或主动脉或混合静脉血的灌注中均无变化。与体外分离的大鼠灌注肺的结果相反,NG-硝基-L-精氨酸甲酯(L-NAME)会增加肺动脉压,但流速最低,但对曲线压力-流量关系影响很小。 L-NAME逆转了对乙酰胆碱和缓激肽的肺血管舒张反应,并增强了对硝酸甘油的肺血管舒张反应。目前的数据表明,主动诱发的肺动脉高压受到内皮源性舒张因子(EDRF)的更大控制。与先前体外灌注大鼠肺中的结果不同,ISBR中的结果表明,对肾上腺髓质素-(13-52)的肺血管舒张反应不是由降钙素基因相关肽受体介导的,而降钙素基因相关肽受体与EDRF的释放无关。这些结果表明,这项新技术可能为研究完整胸大鼠的肺循环提供有用的模型。

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