Determination of right ventricular structure and function in normoxic and hypoxic mice - A transesophageal echocardiographic study

被引:59
作者
Scherrer-Crosbie, M
Steudel, W
Hunziker, PR
Foster, GP
Garrido, L
Liel-Cohen, N
Zapol, WM
Picard, MH
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Med,Cardiac Unit,Cardiac Ultrasound Lab, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Anesthesia & Crit Care, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
关键词
echocardiography; ventricles; hypoxia;
D O I
10.1161/01.CIR.98.10.1015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Noninvasive cardiac evaluation is of great importance in transgenic mice. Transthoracic echocardiography can visualize the left ventricle well but has not been as successful for the right ventricle (RV). We developed a method of transesophageal echocardiography (TEE) to evaluate murine RV size and function. Methods and Results-Normoxic and chronically hypoxic mice (FIO2=0.11, 3 weeks) and agarose RV casts were scanned with a rotating 3.5F/30-MHz intravascular ultrasound probe. In vivo, the probe was inserted in the mouse esophagus and withdrawn to obtain contiguous horizontal planes at 1-mm intervals. In vitro, the probe was withdrawn along the left ventricular posterior wall of excised hearts. The borders of the RV were traced on each plane, allowing calculation of diastolic and systolic volumes, RV mass, RV ejection fraction, stroke volume, and cardiac output. RV wall thickness was measured, Echo volumes obtained in vitro were compared with cast volumes. Echo-derived cardiac output was compared with measurements of an ascending aortic Doppler flow probe. Echo-derived RV free wall mass was compared with true RV free wall weight. There was excellent agreement between cast and TEE volumes (y=0.82x+6.03, r=0.88, P<0.01) and flow-probe and echo cardiac output (y=1.00x+0.45, r=0.99, P<0.0001), Although echo-derived RV mass and wall thickness were well correlated with true RV weight, echo-derived RV mass underestimated true weight (y=0.53x+2.29, r=0.81, P<0.0001). RV mass and wall thickness were greater in hypoxic mice than in normoxic mice (0.78+/-0.19 versus 0.51+/-0.14 mg/g, P<0.03, 0.50+/-0.03 versus 0.38+/-0.03 mm, P<0.04). Conclusions-TEE with an intravascular ultrasound catheter is a simple, accurate, and reproducible method to study RV size and function in mice,
引用
收藏
页码:1015 / 1021
页数:7
相关论文
共 22 条
[1]   STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT [J].
BLAND, JM ;
ALTMAN, DG .
LANCET, 1986, 1 (8476) :307-310
[2]   Renal abnormalities in mutant mice [J].
Carpenter, C ;
Honkanen, AA ;
Mashimo, H ;
Goss, KA ;
Huang, P ;
Fishman, MC ;
Asaad, M ;
Dorso, CR ;
Cheung, HS .
NATURE, 1996, 380 (6572) :292-292
[3]   Genes and physiology: Molecular physiology in genetically engineered animals [J].
Chien, KR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04) :901-909
[4]   The critical role of tissue angiotensin-converting enzyme as revealed by gene targeting in mice [J].
Esther, CR ;
Marino, EM ;
Howard, TE ;
Machaud, A ;
Corvol, P ;
Capecchi, MR ;
Bernstein, KE .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (10) :2375-2385
[5]   ECHOCARDIOGRAPHIC ASSESSMENT OF LEFT-VENTRICULAR MASS AND SYSTOLIC FUNCTION IN MICE [J].
GARDIN, JM ;
SIRI, FM ;
KITSIS, RN ;
EDWARDS, JG ;
LEINWAND, LA .
CIRCULATION RESEARCH, 1995, 76 (05) :907-914
[6]  
Gorge G, 1995, Am J Card Imaging, V9, P180
[7]   IN-VIVO ECHOCARDIOGRAPHIC DETECTION OF ENHANCED LEFT-VENTRICULAR FUNCTION IN GENE-TARGETED MICE WITH PHOSPHOLAMBAN DEFICIENCY [J].
HOIT, BD ;
HOURY, SF ;
KRANIAS, EG ;
BALL, N ;
WALSH, RA .
CIRCULATION RESEARCH, 1995, 77 (03) :632-637
[8]   In vivo determination of left ventricular wall stress-shortening relationship in normal mice [J].
Hoit, BD ;
Khan, ZU ;
PawloskiDahm, CM ;
Walsh, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 272 (02) :H1047-H1052
[9]   HYPERTENSION IN MICE LACKING THE GENE FOR ENDOTHELIAL NITRIC-OXIDE SYNTHASE [J].
HUANG, PL ;
HUANG, ZH ;
MASHIMO, H ;
BLOCH, KD ;
MOSKOWITZ, MA ;
BEVAN, JA ;
FISHMAN, MC .
NATURE, 1995, 377 (6546) :239-242
[10]  
HURFORD WE, 1990, J NUCL MED, V31, P1344