Miserocchi G, Venturoli D, Negrini D, Del Fabbro M
Istituto di Fisiologia Umana, Università degli Studi, Milan, Italy.
J Appl Physiol (1985). 1993 Oct;75(4):1798-806. doi: 10.1152/jappl.1993.75.4.1798.
A model of pleural fluid turnover, based on mass conservation law, was developed from experimental evidence that 1) pleural fluid filters through the parietal pleura and is drained by parietal lymphatics and 2) lymph flow increases after an increase in pleural liquid volume, attaining a maximum value 10 times greater than control. From the differential equation describing the time evolution of pleural liquid pressure, we obtained the equation for the steady-state condition ("set point") of pleural liquid pressure: Pss = (KfPi*+KlPzf)/Kf+Kl), where Kf is parietal pleura filtration coefficient, Kl is initial lymphatic conductance, Pzf is lymphatic potential absorption pressure, and Pi* is a factor accounting for the protein reflection coefficient of parietal mesothelium and hydraulic and colloid osmotic pressure of parietal interstitium and pleural liquid. Lymphatics act as a passive negative-feedback control tending to offset increases in pleural liquid volume. Some features of this control are summarized here: 1) lymphatics exert a tight control on pleural liquid volume or pressure so that the set point is maintained close to the potential absorption pressure of lymphatics; 2) a 10-fold increase in Kf would cause only a 2- and 5-fold increase in pleural liquid volume with normal (1.8 g/dl) and increased (3.4 g/dl) protein concentration of the pleural fluid, respectively; and 3) the reduction in maximum lymph flow greatly reduces the range of operation of the control with increased filtration and/or protein concentration of pleural fluid.
基于质量守恒定律,我们建立了一个胸腔积液周转模型。实验证据表明:1)胸腔积液通过脏层胸膜滤过,并由脏层淋巴管引流;2)胸腔积液量增加后,淋巴流量增加,达到比对照组大10倍的最大值。从描述胸腔积液压力随时间变化的微分方程中,我们得到了胸腔积液压力稳态条件(“设定点”)的方程:Pss = (KfPi*+KlPzf)/Kf+Kl),其中Kf是脏层胸膜滤过系数,Kl是初始淋巴传导率,Pzf是淋巴管潜在吸收压力,Pi*是一个考虑脏层间皮细胞蛋白质反射系数以及脏层间质和胸腔积液的液压和胶体渗透压的因子。淋巴管起到被动负反馈控制的作用,倾向于抵消胸腔积液量的增加。这种控制的一些特点总结如下:1)淋巴管对胸腔积液量或压力进行严格控制,以使设定点保持在接近淋巴管潜在吸收压力的水平;2)Kf增加10倍时,胸腔积液蛋白质浓度正常(1.8 g/dl)和升高(3.4 g/dl)时,胸腔积液量分别仅增加2倍和5倍;3)最大淋巴流量的降低极大地缩小了在胸腔积液滤过增加和/或蛋白质浓度增加时控制的作用范围。