Rippe B, Haraldsson B
Department of Physiology, University of Göteborg, Sweden.
Acta Physiol Scand. 1987 Nov;131(3):411-28. doi: 10.1111/j.1748-1716.1987.tb08257.x.
Treating the blood-tissue barrier as a two-pore membrane the separate fluid and solute fluxes occurring across 'small pores' and 'large pores' were modelled in continuous capillaries employing two-pore equations for the calculations together with the non-linear flux equation and theories for restricted diffusion and for the reflection coefficient (sigma). The two-pore equations derived proved useful for analyses of transvascular protein flux data obtained at low as well as at high filtration rates. These equations were applied to lymphatic protein flux data from dog paw (Renkin et al. 1977a, b) and to tracer albumin uptake data from rat skeletal muscle (Rippe et al. 1979). For both sets of data the small- and large-pore radii became closely similar, 44 vs. 45 A and 240 vs. 225 A, which also holds for the large-pore fractions of hydraulic conductivity (0.097 vs. 0.056). The main result of this analysis is that the passage of macromolecules normally occurring across the microvascular walls is almost entirely convective, and hence, dependent on the transmural hydrostatic and oncotic pressure gradients and on the hydraulic conductivity. For example, 75-90% of the transvascular passage of albumin was found to be due to convection through large pores at normal lymph flows, the remaining portion being mainly due to diffusion across small pores. Solutes larger than albumin were almost exclusively transported by convection across large pores. Two-pore heterogeneity was found to explain the previously observed variations of the apparent overall large solute diffusion capacity (PSapp) and the overall reflection coefficient (sigma f) with filtration rate and also previous overestimations of PS. Furthermore, the present results were not compatible with protein transport across any 'non-hydraulically conductive capillary pathways' as previously postulated from the lymphatic protein flux data analysed here (Renkin 1985).
将血 - 组织屏障视为双孔膜,在连续毛细血管中,利用双孔方程结合非线性通量方程以及受限扩散和反射系数(σ)理论,对跨“小孔”和“大孔”发生的单独的流体和溶质通量进行建模计算。所推导的双孔方程被证明对于分析在低滤过率和高滤过率下获得的跨血管蛋白质通量数据很有用。这些方程被应用于狗爪的淋巴蛋白质通量数据(Renkin等人,1977a,b)以及大鼠骨骼肌的示踪白蛋白摄取数据(Rippe等人,1979)。对于这两组数据,小孔半径和大孔半径非常接近,分别为44 Å对45 Å和240 Å对225 Å,这对于水力传导率的大孔分数(0.097对0.056)也成立。该分析的主要结果是,通常在微血管壁上发生的大分子通过几乎完全是对流性的,因此,取决于跨壁静水压力和胶体渗透压梯度以及水力传导率。例如,发现在正常淋巴流量下,75 - 90%的白蛋白跨血管通过是由于通过大孔的对流,其余部分主要是由于通过小孔的扩散。大于白蛋白的溶质几乎完全通过大孔的对流进行运输。发现双孔异质性可以解释先前观察到的表观总体大溶质扩散能力(PSapp)和总体反射系数(σf)随滤过率的变化,以及先前对PS的高估。此外,目前的结果与通过任何“非水力传导性毛细血管途径”的蛋白质运输不相符,正如先前从这里分析的淋巴蛋白质通量数据所假设的那样(Renkin,1985)。