Measurement of in vivo myocardial microcirculatory function with electron beam CT

被引:45
作者
Lerman, LO
Siripornpitak, S
Maffei, NL
Sheedy, PF
Ritman, EL
机构
[1] Mayo Clin, Dept Internal Med, Div Hypertens, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Diagnost Radiol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Physiol & Biophys, Rochester, MN 55905 USA
关键词
computed tomography; techniques; myocardium; microcirculation;
D O I
10.1097/00004728-199905000-00013
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: The purpose of this work was to examine the capability of electron beam CT (EBCT) to characterize responses of recruitable (capillaries and small arterioles) compared with nonrecruitable (small to large arterioles) myocardial microvessels to vasoactive substances. Method: Myocardial perfusion (F) and total intramyocardial blood volume (BV) of the anterior cardiac wall were quantitated in 36 pigs, using EBCT and intravenous contrast agent injections, before and after intracoronary administration of either NG-monomethyl-L-arginine (L-NMMA), nitroglycerin, adenosine, or saline. Plotting the relationship of BV and F provided values for the recruitable and nonrecruitable microvascular transit times and BV allotment. Results: Nitroglycerin increased nonrecruitable BV by 84.5 +/- 7.4%, whereas adenosine increased both recruitable and nonrecruitable microvascular BV(47.1 +/- 18.9 and 66.0 +/- 10.9%, respectively). L-NMMA led to a 25.1% decrease only in the recruitable BV. In the control group, no changes were observed. Conclusion: Characteristic responses of different-size myocardial microvessels may be inferred with EBCT, which provides a unique opportunity to portray intramyocardial microcirculatory function noninvasively.
引用
收藏
页码:390 / 398
页数:9
相关论文
共 41 条
[11]  
HARRISON DG, 1994, BASIC RES CARDIOL, V89, P87
[12]  
HAYBALL M, 1997, FUNCTIONAL COMPUTED, P7
[13]   CHRONIC INHIBITION OF ENDOTHELIUM-DERIVED NITRIC-OXIDE SYNTHESIS CAUSES CORONARY MICROVASCULAR STRUCTURAL-CHANGES AND HYPERREACTIVITY TO SEROTONIN IN PIGS [J].
ITO, A ;
EGASHIRA, K ;
KADOKAMI, T ;
FUKUMOTO, Y ;
TAKAYANAGI, T ;
NAKAIKE, R ;
KUGA, T ;
SUEISHI, K ;
SHIMOKAWA, H ;
TAKESHITA, A .
CIRCULATION, 1995, 92 (09) :2636-2644
[14]  
KANATSUKA H, 1992, J CARDIOVASC PHARM, V19, P755
[15]   HETEROGENEOUS CHANGES IN EPIMYOCARDIAL MICROVASCULAR SIZE DURING GRADED CORONARY STENOSIS - EVIDENCE OF THE MICROVASCULAR SITE FOR AUTOREGULATION [J].
KANATSUKA, H ;
LAMPING, KG ;
EASTHAM, CL ;
MARCUS, ML .
CIRCULATION RESEARCH, 1990, 66 (02) :389-396
[16]   COMPARISON OF THE EFFECTS OF INCREASED MYOCARDIAL OXYGEN-CONSUMPTION AND ADENOSINE ON THE CORONARY MICROVASCULAR RESISTANCE [J].
KANATSUKA, H ;
LAMPING, KG ;
EASTHAM, CL ;
DELLSPERGER, KC ;
MARCUS, ML .
CIRCULATION RESEARCH, 1989, 65 (05) :1296-1305
[17]  
Kaul S, 1997, CIRCULATION, V96, P719
[18]  
KAYAR SR, 1991, MICROCIRC ENDOTH LYM, V7, P77
[19]   EFFECT OF AN ARGININE ANALOG ON ACETYLCHOLINE-INDUCED CORONARY MICROVASCULAR DILATATION IN DOGS [J].
KOMARU, T ;
LAMPING, KG ;
EASTHAM, CL ;
HARRISON, DG ;
MARCUS, ML ;
DELLSPERGER, KC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (06) :H2001-H2007
[20]   LONGITUDINAL GRADIENTS FOR ENDOTHELIUM-DEPENDENT AND ENDOTHELIUM-INDEPENDENT VASCULAR-RESPONSES IN THE CORONARY MICROCIRCULATION [J].
KUO, L ;
DAVIS, MJ ;
CHILIAN, WM .
CIRCULATION, 1995, 92 (03) :518-525