Balance between myogenic, flow-dependent, and metabolic flow control in coronary arterial tree: a model study

被引:78
作者
Cornelissen, AJM
Dankelman, J
VanBavel, E
Spaan, JAE
机构
[1] Univ Amsterdam, Acad Med Ctr, Cardiovasc Res Inst Amsterdam, Dept Med Phys, NL-1105 AZ Amsterdam, Netherlands
[2] Delft Univ Technol, Fac Design Engn & Prod, Dept Med Technol & Mech, Man Machine Syst & Control Grp, NL-2628 CD Delft, Netherlands
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2002年 / 282卷 / 06期
关键词
myogenic response; flow-dependent dilation; metabolic control; autoregulation; mathematical model;
D O I
10.1152/ajpheart.00491.2001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myogenic response, flow-dependent dilation, and direct metabolic control are important mechanisms controlling coronary flow. A model was developed to study how these control mechanisms interact at different locations in the arteriolar tree and to evaluate their contribution to autoregulatory and metabolic flow control. The model consists of 10 resistance compartments in series, each representing parallel vessel units, with their diameters determined by tone depending on either flow and pressure [flow-dependent tone reduction factor (TRFflow) x Tone(myo)] or directly on metabolic factors (Tone(meta)). The pressure-Tone(myo) and flow-TRFflow relations depend on the vessel size obtained from interpolation of data on isolated vessels. Flow-dependent dilation diminishes autoregulatory properties compared with pressure-flow lines obtained from vessels solely influenced by Tonemyo. By applying Tonemeta to the four distal compartments, the autoregulatory properties are restored and tone is equally distributed over the compartments. Also, metabolic control and blockage of nitric oxide are simulated. We conclude that a balance is required between the flow-dependent properties upstream and the constrictive metabolic properties downstream. Myogenic response contributes significantly to flow regulation.
引用
收藏
页码:H2224 / H2237
页数:14
相关论文
共 43 条
[1]   REDISTRIBUTION OF CORONARY MICROVASCULAR RESISTANCE PRODUCED BY DIPYRIDAMOLE [J].
CHILIAN, WM ;
LAYNE, SM ;
KLAUSNER, EC ;
EASTHAM, CL ;
MARCUS, ML .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (02) :H383-H390
[2]   CORONARY MICROVASCULAR RESPONSES TO REDUCTIONS IN PERFUSION-PRESSURE - EVIDENCE FOR PERSISTENT ARTERIOLAR VASOMOTOR TONE DURING CORONARY HYPOPERFUSION [J].
CHILIAN, WM ;
LAYNE, SM .
CIRCULATION RESEARCH, 1990, 66 (05) :1227-1238
[3]   MICROVASCULAR DISTRIBUTION OF CORONARY VASCULAR-RESISTANCE IN BEATING LEFT-VENTRICLE [J].
CHILIAN, WM ;
EASTHAM, CL ;
MARCUS, ML .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (04) :H779-H788
[4]   Elevated capillary tube hematocrit reflects degradation of endothelial cell glycocalyx by oxidized LDL [J].
Constantinescu, AA ;
Vink, H ;
Spaan, JAE .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2001, 280 (03) :H1051-H1057
[5]   Myogenic reactivity and resistance distribution in the coronary arterial tree: a model study [J].
Cornelissen, AJM ;
Dankelman, J ;
VanBavel, E ;
Stassen, HG ;
Spaan, JAE .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (05) :H1490-H1499
[6]   MYOGENIC RESPONSE GRADIENT IN AN ARTERIOLAR NETWORK [J].
DAVIS, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (06) :H2168-H2179
[7]   Regulation of coronary vasomotor tone under normal conditions and during acute myocardial hypoperfusion [J].
Duncker, DJ ;
Bache, RJ .
PHARMACOLOGY & THERAPEUTICS, 2000, 86 (01) :87-110
[8]   CORONARY PHYSIOLOGY [J].
FEIGL, EO .
PHYSIOLOGICAL REVIEWS, 1983, 63 (01) :1-205
[9]   COMPLIANCE OF ISOLATED PORCINE CORONARY SMALL ARTERIES AND CORONARY PRESSURE-FLOW RELATIONS [J].
GIEZEMAN, MJMM ;
VANBAVEL, E ;
GRIMBERGEN, CA ;
SPANN, JAE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (03) :H1190-H1198
[10]   Vasodilatory effect of pulsatile pressure on coronary resistance vessels [J].
Goto, M ;
VanBavel, E ;
Giezeman, MJMM ;
Spaan, JAE .
CIRCULATION RESEARCH, 1996, 79 (05) :1039-1045