Interconnected-tubes model of hepatic elimination: Steady-state considerations

被引:4
作者
Anissimov, YG
Bracken, AJ
Roberts, MS [1 ]
机构
[1] Univ Queensland, Princess Alexandra Hosp, Dept Med, Woolloongabba, Qld 4102, Australia
[2] Univ Queensland, Dept Math, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1006/jtbi.1999.0970
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the interconnected-tubes model of hepatic transport and elimination, intermixing between sinusoids was modelled by the continuous interchange of solutes between a set of parallel tubes. In the case of strongly interconnected tubes and for bolus input of solute, a zeroth-order approximation led to the governing equation of the dispersion model. The dispersion number was expressed for the first time in terms of its main physiological determinants: heterogeneity of flow and density of interconnections. The interconnected-tubes model is now applied to steady-state hepatic extraction. In the limit of strong interconnections, the expression for output concentrations is predicted to be similar in form to those predicted by the distributed model for a narrow distribution of elimination rates over sinusoids, and by the dispersion model in the limit of a small dispersion number D-N. More generally, the equations for the predicted output concentrations can be expressed in terms of a dimensionless 'heterogeneity number' H-N, which characterizes the combined effects of variations in enzyme distribution and flow rates between different sinusoids, together with the effects of interconnections between sinusoids. A comparative analysis of the equations for the dispersion and heterogeneity numbers shows that the value of H-N can be less than, greater than or equal to the value of D-N for a correlation between distributions of velocities and elimination rates over sinusoids, anticorrelation between them, and when all sinusoids have the same elimination rate, respectively. Simple model systems are used to illustrate the determinants of H-N and D-N. (C) 1999 Academic Press.
引用
收藏
页码:435 / 447
页数:13
相关论文
共 33 条
[1]   Interconnected-tubes model of hepatic elimination [J].
Anissimov, YG ;
Bracken, AJ ;
Roberts, MS .
JOURNAL OF THEORETICAL BIOLOGY, 1997, 188 (01) :89-101
[2]   ON THE RELATION BETWEEN EXTENDED FORMS OF THE SINUSOIDAL PERFUSION AND OF THE CONVECTION DISPERSION MODELS OF HEPATIC ELIMINATION [J].
BASS, L ;
ROBERTS, MS ;
ROBINSON, PJ .
JOURNAL OF THEORETICAL BIOLOGY, 1987, 126 (04) :457-482
[3]   PHYSIOLOGICALLY BASED MODELS AND STRATEGIC EXPERIMENTS IN HEPATIC PHARMACOLOGY [J].
BASS, L ;
KEIDING, S .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (08) :1425-1431
[5]   HEPATIC ELIMINATION OF FLOWING SUBSTRATES - DISTRIBUTED MODEL [J].
BASS, L ;
ROBINSON, P ;
BRACKEN, AJ .
JOURNAL OF THEORETICAL BIOLOGY, 1978, 72 (01) :161-184
[6]  
BASS L, 1976, Journal of Theoretical Biology, V61, P393, DOI 10.1016/0022-5193(76)90026-6
[7]   STATISTICAL-MECHANICS OF HEPATIC ELIMINATION [J].
BRACKEN, AJ ;
BASS, L .
MATHEMATICAL BIOSCIENCES, 1979, 44 (1-2) :97-120
[8]  
CHOU CH, 1993, DRUG METAB DISPOS, V21, P933
[9]   INFLUENCE OF ALBUMIN ON THE DISTRIBUTION AND ELIMINATION KINETICS OF DICLOFENAC IN THE ISOLATED PERFUSED-RAT-LIVER - ANALYSIS BY THE IMPULSE-RESPONSE TECHNIQUE AND THE DISPERSION MODEL [J].
EVANS, AM ;
HUSSEIN, Z ;
ROWLAND, M .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1993, 82 (04) :421-428
[10]  
GORESKY CA, 1963, AM J PHYSIOL, V204, P626