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In vivo determination of collecting lymphatic vessel permeability to albumin: a role for lymphatics in exchange

机译:体内测定收集淋巴管对白蛋白的通透性:淋巴管在交换中的作用

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摘要

While it is well established that the lymphatic vasculature is central to fluid and solute homeostasis, how it accomplishes this task is not well defined. To clarify the basic mechanisms underlying basal fluid and solute homeostasis, we assessed permeability to rat serum albumin () in mesenteric collecting lymphatic vessels and venules of juvenile male rats. Using the quantitative microfluorometric technique originally developed for blood capillaries, we tested the hypothesis that as a consequence of venules and collecting lymphatics sharing a common embryological origin, their would not differ significantly. Supporting our hypothesis, the median collecting lymphatic (3.5 ± 1.0 × 10−7 cm s−1, N= 22) did not differ significantly from the median venular (4.0 ± 1.0 × 10−7 cm s−1, N= 8, P= 0.61). For collecting lymphatics the diffusive permeability (Pd= 2.5 × 10−7 cm s−1) was obtained from the relationship of apparent and pressure. While the measured , Pd and estimated hydraulic conductivity of collecting lymphatics and venules were similar, the contribution of convective coupling differs as a result of the higher hydrostatic pressure experienced by venules relative to collecting lymphatics in vivo. In summary, the data demonstrate the capacity for collecting lymphatics to act as exchange vessels, able to extravasate solute and filter fluid. As a consequence these data provide experimental support for the theory that prenodal lymphatic vessels concentrate intraluminal protein.
机译:众所周知,淋巴管是流体和溶质稳态的关键,但如何完成这项任务的方法尚不清楚。为了阐明基础液和溶质稳态的基本机制,我们评估了雄性大鼠肠系膜收集淋巴管和小静脉对大鼠血清白蛋白的渗透性。使用最初为血液毛细血管开发的定量微荧光技术,我们检验了以下假设:由于小静脉和收集具有共同胚胎起源的淋巴管,它们的差异不会显着。支持我们的假设,中位收集淋巴管(3.5±1.0×10 −7 cm s −1 ,N = 22)与中位静脉(4.0± 1.0×10 −7 cm s −1 ,N = 8,P = 0.61)。为了收集淋巴管,根据表观压力与压力的关系获得扩散渗透率(Pd = 2.5×10 −7 cm s -1 )。尽管收集的淋巴管和小静脉的测得的,Pd和估计的水力传导率相似,但由于小静脉相对于体内收集淋巴管的静水压力较高,对流耦合的作用也有所不同。总之,数据证明了收集淋巴管作为交换血管的能力,能够渗出溶质并过滤液体。结果,这些数据为结节前淋巴管浓缩腔内蛋白的理论提供了实验支持。

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