A nonlinear model for myogenic regulation of blood flow to bone: Equilibrium states and stability characteristics

Timothy P. Harrigan

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

A simple compartmental model for myogenic regulation of interstitial pressure in bone is developed, and the interaction between changes in interstitial pressure and changes in arterial and venous resistances is studied. The arterial resistance is modeled by a myogenic model that depends on transmural pressure, and the venous resistance is modeled by using a vascular waterfall. Two series capacitances model blood storage in the vascular system and interstitial fluid storage in the extravascular space. The static results mimic the observed effect that vasodilators work less well in bone than do vasoconstrictors. The static results also show that the model gives constant flow rates over a limited range of arterial pressure. The dynamic model shows unstable behavior at small values of bony capacitance and at high enough myogenic gain. At low myogenic gain, only a single equilibrium state is present, but at high enough myogenic gain, two new equilibrium states appear. At additional increases in gain, one of the two new states merges with and then separates from the original state, and the original state becomes a saddle point. The appearance of the new states and the transition of the original state to a saddle point do not depend on the bony capacitance, and these results are relevant to general fluid compartments. Numerical integration of the rate equations confirms the stability calculations and shows limit cycling behavior in several situations. The relevance of this model to circulation in bone and to other compartments is discussed.

Original languageEnglish (US)
Pages (from-to)211-221
Number of pages11
JournalAnnals of biomedical engineering
Volume24
Issue number2
DOIs
StatePublished - Jan 1 1996
Externally publishedYes

Keywords

  • Compartmental model
  • Fluid capacitance
  • Limit cycling

ASJC Scopus subject areas

  • Biomedical Engineering

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