PULMONARY MICROCIRCULATORY HEMODYNAMICS
肺微循环血流动力学
基本信息
- 批准号:3350559
- 负责人:
- 金额:$ 11.44万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1989
- 资助国家:美国
- 起止时间:1989-07-01 至 1991-06-30
- 项目状态:已结题
- 来源:
- 关键词:blood pressure capillary bed cardiac output densitometry dogs dyes erythrocytes fluorescence microscopy hemodynamics mathematical model microcirculation neural information processing neutrophil prostaglandins pulmonary artery pulmonary circulation radiotracer respiratory airway pressure respiratory function respiratory gas transport sympathetic nervous system vascular endothelium permeability vascular resistance
项目摘要
The time that blood spends in the pulmonary capillaries is a major
determinant of the gas exchange effectiveness of the lungs. Consequently,
physiologic mechanisms which alter this contact time may serve important
regulatory functions. For example, during exercise some factors reduce
contact time so that more red blood cells traverse the capillaries per unit
time, thereby enhancing gas exchange. If, however, transit times become
too rapid, arterial hypoxemia can result. The obvious importance of
understanding how pulmonary microcirculatory hemodynamics are regulated
have prompted numerous studies, but previous investigators have been forced
to use indirect techniques and, in terms of red blood cell capillary
transit time, to consider the lung as a single, homogeneous entity. In
fact, it is likely that regional differences in pressure and flow within
the lung give rise to regional differences in capillary transit. Using in
vivo video fluorescence microscopy techniques recently developed by us, we
propose to determine directly the length of time required for red blood
cells to traverse pulmonary capillaries and to evaluate how transit time
changes as a function of physiologic variables (pulmonary arterial and
venous pressures, cardiac output, and pulmonary capillary recruitment).
Specific emphasis is placed on studying mechanisms that reduce transit time
in order to increase gas exchange. Finally, we will determine the site of
sequestration and transit time of fluorescein labeled neutrophils when the
cells are normal and activated.
血液在肺毛细血管中停留的时间是重要的
肺的气体交换效率的决定因素。 最后,
改变接触时间的生理机制可能发挥重要作用
监管职能。 例如,在运动过程中,某些因素会降低
接触时间使每单位有更多的红细胞穿过毛细血管
时间,从而增强气体交换。 然而,如果运输时间变成
太快,可能导致动脉低氧血症。 显而易见的重要性
了解肺微循环血流动力学如何调节
引发了大量研究,但之前的研究人员被迫
使用间接技术,就红细胞毛细血管而言
通过时间,将肺视为一个单一的、同质的实体。 在
事实上,内部压力和流量的区域差异很可能是存在的。
肺部引起毛细血管运输的区域差异。 使用于
我们最近开发的活体视频荧光显微镜技术,我们
建议直接确定红血需要的时间长度
细胞穿过肺毛细血管并评估通过时间
作为生理变量(肺动脉和
静脉压、心输出量和肺毛细血管募集)。
特别强调研究减少运输时间的机制
以增加气体交换。 最后我们将确定站点
荧光素标记的中性粒细胞的隔离和转运时间
细胞正常且激活。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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WILTZ WALKER WAGNER其他文献
WILTZ WALKER WAGNER的其他文献
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{{ truncateString('WILTZ WALKER WAGNER', 18)}}的其他基金
MECHANISMS OF NEUTROPHIL MARGINATION IN THE NORMAL LUNG
正常肺中性粒细胞边缘的机制
- 批准号:
2222887 - 财政年份:1992
- 资助金额:
$ 11.44万 - 项目类别:
MECHANISMS OF NEUTROPHIL MARGINATION IN THE NORMAL LUNG
正常肺中性粒细胞边缘的机制
- 批准号:
3365537 - 财政年份:1992
- 资助金额:
$ 11.44万 - 项目类别:
MECHANISMS OF NEUTROPHIL MARGINATION IN THE NORMAL LUNG
正常肺中性粒细胞边缘的机制
- 批准号:
3365536 - 财政年份:1992
- 资助金额:
$ 11.44万 - 项目类别:
MECHANISMS OF NEUTROPHIL MARGINATION IN THE NORMAL LUNG
正常肺中性粒细胞边缘的机制
- 批准号:
2222886 - 财政年份:1992
- 资助金额:
$ 11.44万 - 项目类别:
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- 资助金额:
$ 11.44万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)














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