Barer G R, Bee D, Wach R A
J Physiol. 1983 Mar;336:27-38. doi: 10.1113/jphysiol.1983.sp014563.
A rat model was used to assess the viscosity factor in pulmonary hypertension of high altitude. Rats exposed to 10% O2 for three weeks developed increased pulmonary vascular resistance (p.v.r.) and polycythaemia; the haematocrit (Hct) was 50-60%, values similar to those in normal men at high altitudes. The contribution of high Hct to the increased p.v.r. was assessed in isolated perfused lungs of chronically hypoxic rats perfused with their own high Hct blood, or normal Hct blood from control rats. Pressure/flow relationships were measured over a wide range and the slope (P/Q) of this relationship and its extrapolated intercept on the pressure axis were increased by high Hct blood. A return to low Hct blood did not restore initial conditions although a second perfusion with high Hct blood again increased p.v.r. and intercept. Lack of reversibility was attributed to changes with time in blood or lung. In a second experiment designed to eliminate time changes, chronically hypoxic or litter-mate control rats were each perfused with only one blood, their own or each other's and P/Q relations were rapidly measured. The P/Q slope and pressure intercept increased progressively in the following groups: control rats perfused with their own blood (Hct 34%), control rats perfused with chronically hypoxic blood (Hct 56%), chronically hypoxic rats perfused with control blood (Hct 35%) and chronically hypoxic rats perfused with chronically hypoxic blood (Hct 53%). To exclude factors in chronically hypoxic blood other than high Hct which might increase p.v.r., control rats were perfused with blood of different Hct obtained by centrifugation. High Hct again increased p.v.r. There was a significant relationship in all rats between pulmonary artery pressure (Ppa), which takes into account both P/Q slope, intercept and Hct. There was substantial batch variation which may reflect sensitivity to hypoxia. In chronically hypoxic rats with high Hct blood, Ppa varied from 29-47 mmHg; with low Hct blood the range was 26-38 mmHg. Comparable values for control rats were 21-29 and 17-20 mmHg. We conclude that the polycythaemic blood of chronic hypoxia contributes substantially to pulmonary hypertension. Where it is excessive, it may prejudice tissue blood flow.
采用大鼠模型评估高原肺动脉高压中的黏度因素。将大鼠置于10%氧气环境中3周,其肺血管阻力(p.v.r.)增加且出现红细胞增多症;血细胞比容(Hct)为50 - 60%,这与正常男性在高原时的值相似。通过用慢性低氧大鼠自身的高Hct血液或对照大鼠的正常Hct血液灌注其离体灌注肺,评估高Hct对p.v.r.升高的影响。在较宽范围内测量压力/流量关系,高Hct血液会使该关系的斜率(P/Q)及其在压力轴上的外推截距增加。尽管再次用高Hct血液灌注会再次增加p.v.r.和截距,但恢复到低Hct血液时并未恢复初始状态。不可逆性归因于血液或肺随时间的变化。在第二个旨在消除时间变化的实验中,将慢性低氧大鼠或同窝对照大鼠分别仅用一种血液(自身的或彼此的)进行灌注,并快速测量P/Q关系。在以下几组中,P/Q斜率和压力截距逐渐增加:用自身血液(Hct 34%)灌注的对照大鼠、用慢性低氧血液(Hct 56%)灌注的对照大鼠、用对照血液(Hct 35%)灌注的慢性低氧大鼠以及用慢性低氧血液(Hct 53%)灌注的慢性低氧大鼠。为排除慢性低氧血液中除高Hct之外可能增加p.v.r.的因素,用通过离心获得的不同Hct的血液灌注对照大鼠。高Hct再次增加了p.v.r.。在所有大鼠中,考虑到P/Q斜率、截距和Hct的肺动脉压力(Ppa)之间存在显著关系。存在大量批次差异,这可能反映了对缺氧的敏感性。在高Hct血液的慢性低氧大鼠中,Ppa在29 - 47 mmHg之间变化;低Hct血液时范围为26 - 38 mmHg。对照大鼠的可比数值为21 - 29 mmHg和17 - 20 mmHg。我们得出结论,慢性缺氧的红细胞增多血液对肺动脉高压有很大影响。如果红细胞增多过度,可能会损害组织血流。