4.3 Article

Balance point characterization of interstitial fluid volume regulation

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00097.2009

Keywords

edemagenic gain; mathematical modeling; edema

Categories

Funding

  1. National Heart, Lung, and Blood Institute [K25-HL-070608]
  2. American Heart Association [0565116Y, 0365127Y]
  3. Center for Disease Control [623086]

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Dongaonkar RM, Laine GA, Stewart RH, Quick CM. Balance point characterization of interstitial fluid volume regulation. Am J Physiol Regul Integr Comp Physiol 297: R6-R16, 2009. First published May 6, 2009; doi:10.1152/ajpregu.00097.2009.-The individual processes involved in interstitial fluid volume and protein regulation (microvascular filtration, lymphatic return, and interstitial storage) are relatively simple, yet their interaction is exceedingly complex. There is a notable lack of a first-order, algebraic formula that relates interstitial fluid pressure and protein to critical parameters commonly used to characterize the movement of interstitial fluid and protein. Therefore, the purpose of the present study is to develop a simple, transparent, and general algebraic approach that predicts interstitial fluid pressure (P-i) and protein concentrations (C-i) that takes into consideration all three processes. Eight standard equations characterizing fluid and protein flux were solved simultaneously to yield algebraic equations for P-i and C-i as functions of parameters characterizing microvascular, interstitial, and lymphatic function. Equilibrium values of P-i and C-i arise as balance points from the graphical intersection of transmicrovascular and lymph flows (analogous to Guyton's classical cardiac output-venous return curves). This approach goes beyond describing interstitial fluid balance in terms of conservation of mass by introducing the concept of inflow and outflow resistances. Algebraic solutions demonstrate that P-i and C-i result from a ratio of the microvascular filtration coefficient (1/inflow resistance) and effective lymphatic resistance (outflow resistance), and Pi is unaffected by interstitial compliance. These simple algebraic solutions predict P-i and C-i that are consistent with reported measurements. The present work therefore presents a simple, transparent, and general balance point characterization of interstitial fluid balance resulting from the interaction of microvascular, interstitial, and lymphatic function.

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