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淋巴结转运过程中淋巴蛋白浓度变化的定量分析。

Quantitation of changes in lymph protein concentration during lymph node transit.

作者信息

Adair T H, Moffatt D S, Paulsen A W, Guyton A C

出版信息

Am J Physiol. 1982 Sep;243(3):H351-9. doi: 10.1152/ajpheart.1982.243.3.H351.

Abstract

Many investigators assume the protein concentration and colloid osmotic pressure of interstitial fluid and lymph to be identical even after the lymph has passed through a lymph node. We quantitated the degree of modification of lymph by the dog popliteal lymph node by perfusing isolated lymph nodes in situ at physiological flow rates with homologous plasma or plasma diluted to low protein concentration. This enabled us to compare directly prenodal and postnodal lymph flows and protein concentrations. When undiluted plasma was infused into the node, fluid filtered from the blood into the lymph, diluting the lymph. When diluted plasma was infused, fluid was absorbed from the lymph, concentrating the lymph. Nearly all (98%) of the change in lymph protein concentration could be explained by transfer of protein-free fluid either into or out of the lymph. However, when the nodes were perfused with lymph having a colloid osmotic pressure that exactly balanced the hydrostatic and osmotic forces acting across the lymph node blood-lymph barrier, the lymph was not modified during nodal transit. This "equilibrium colloid osmotic pressure" averaged 60% of that of plasma. The concentrating-diluting mechanism became more significant as the perfusion rate decreased and/or as the colloid osmotic pressure of the afferent lymph was made progressively greater than or less than the equilibrium colloid osmotic pressure. We conclude that lymph nodes modify lymph protein concentration and colloid osmotic pressure except when these are already at equilibrium values for given lymph node conditions. Therefore, the assumption that postnodal lymph is representative of interstitial fluid, especially at low but still physiological lymph flows, is likely to be incorrect.

摘要

许多研究者认为,即使淋巴液已经通过了淋巴结,组织间液和淋巴液的蛋白质浓度及胶体渗透压仍是相同的。我们通过以生理流速对犬腘淋巴结进行原位灌注同源血浆或稀释至低蛋白浓度的血浆,来定量犬腘淋巴结对淋巴液的改变程度。这使我们能够直接比较淋巴结前和淋巴结后淋巴液的流量及蛋白质浓度。当向淋巴结内注入未稀释的血浆时,液体从血液滤入淋巴液,使淋巴液稀释。当注入稀释血浆时,液体从淋巴液中被吸收,使淋巴液浓缩。淋巴液蛋白质浓度变化的几乎所有部分(98%)都可以通过无蛋白液体进出淋巴液的转移来解释。然而,当用胶体渗透压恰好平衡作用于淋巴结血 - 淋巴屏障的静水压和渗透压的淋巴液灌注淋巴结时,淋巴液在经过淋巴结的过程中并未发生改变。这种“平衡胶体渗透压”平均为血浆胶体渗透压的60%。随着灌注速率降低和/或随着输入淋巴液的胶体渗透压逐渐高于或低于平衡胶体渗透压,浓缩 - 稀释机制变得更加显著。我们得出结论,淋巴结会改变淋巴液的蛋白质浓度和胶体渗透压,除非这些指标在给定的淋巴结条件下已处于平衡值。因此,认为淋巴结后淋巴液代表组织间液的假设,尤其是在低但仍为生理淋巴液流量时,可能是不正确的。

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