Influence of substrate supply on cardiac efficiency, as measured by pressure-volume analysis in ex vivo mouse hearts

被引:80
作者
How, OJ [1 ]
Aasum, E
Kunnathu, S
Severson, DL
Myhre, ESP
Larsen, TS
机构
[1] Univ Tromso, Fac Med, Inst Med Biol, Dept Med Physiol, N-9037 Tromso, Norway
[2] Univ Calgary, Fac Med, Dept Pharmacol & Therapeut, Calgary, AB T2N 4N1, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2005年 / 288卷 / 06期
关键词
oxygen consumption; pressure-volume area; cardiac metabolism; compliance; steady state;
D O I
10.1152/ajpheart.00084.2005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the present study, we tested the reliability of measurements of pressure-volume area (PVA) and oxygen consumption (M(V)over dot(O2)) in ex vivo mouse hearts, combining the use of a miniaturized conductance catheter and a fiber-optic oxygen sensor. Second, we tested whether we could reproduce the influence of increased myocardial fatty acid (FA) metabolism on cardiac efficiency in the isolated working mouse heart model, which has already been documented in large animal models. The hearts were perfused with crystalloid buffer containing 11 mM glucose and two different concentrations of FA bound to 3% BSA. The initial concentration was 0.3 +/- 0.1 mM, which was subsequently raised to 0.9 +/- 0.1 mM. End-systolic and end-diastolic pressure-volume relationships were assessed by temporarily occluding the preload line. Different steady-state PVA-M(V)over dot(O2) relationships were obtained by changing the loading conditions (pre- and afterload) of the heart. There were no apparent changes in baseline cardiac performance or contractile efficiency (slope of the PVA-M(V)over dot(O2) regression line) in response to the elevation of the perfusate FA concentration. However, all hearts (n = 8) showed an increase in the y-intercept of the PVA-M(V)over dot(O2) regression line after elevation of the palmitate concentration, indicating an FA-induced increase in the unloaded M(V)over dot(O2). Therefore, in the present model, unloaded M(V)over dot(O2) is not independent of metabolic substrate. This is, to our knowledge, the first report of a PVA-M(V)over dot(O2) relationship in ex vivo perfused murine hearts, using a pressure-volume catheter. The methodology can be an important tool for phenotypic assessment of the relationship among metabolism, contractile performance, and cardiac efficiency in various mouse models.
引用
收藏
页码:H2979 / H2985
页数:7
相关论文
共 33 条
[1]   Age-dependent changes in metabolism, contractile function, and ischemic sensitivity in hearts from db/db mice [J].
Aasum, E ;
Hafstad, AD ;
Severson, DL ;
Larsen, TS .
DIABETES, 2003, 52 (02) :434-441
[2]   Cardiac function and metabolism in Type 2 diabetic mice after treatment with BM 17.0744, a novel PPAR-α activator [J].
Aasum, E ;
Belke, DD ;
Severson, DL ;
Riemersma, RA ;
Cooper, M ;
Andreassen, M ;
Larsen, TS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (03) :H949-H957
[3]   CONTINUOUS MEASUREMENT OF LEFT-VENTRICULAR VOLUME IN ANIMALS AND HUMANS BY CONDUCTANCE CATHETER [J].
BAAN, J ;
VANDERVELDE, ET ;
DEBRUIN, HG ;
SMEENK, GJ ;
KOOPS, J ;
VANDIJK, AD ;
TEMMERMAN, D ;
SENDEN, J ;
BUIS, B .
CIRCULATION, 1984, 70 (05) :812-823
[4]   Altered metabolism causes cardiac dysfunction in perfused hearts from diabetic (db/db) mice [J].
Belke, DD ;
Larsen, TS ;
Gibbs, EM ;
Severson, DL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 279 (05) :E1104-E1113
[5]   Glucose and fatty acid metabolism in the isolated working mouse heart [J].
Belke, DD ;
Larsen, TS ;
Lopaschuk, GD ;
Severson, DL .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 277 (04) :R1210-R1217
[6]   UNCOUPLING ACTIVITY OF LONG-CHAIN FATTY ACIDS [J].
BORST, P ;
LOOS, JA ;
CHRIST, EJ ;
SLATER, EC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1962, 62 (03) :509-&
[7]   Effect of Treppe on isovolumic function in the isolated blood-perfused mouse heart [J].
Brooks, WW ;
Apstein, CS .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1996, 28 (08) :1817-1822
[8]  
BURKHOFF D, 1991, AM J PHYSIOL, V261, P741
[9]   Cardiovascular phenotyping in mice [J].
Doevendans, PA ;
Daemen, MJ ;
de Muinck, ED ;
Smits, JF .
CARDIOVASCULAR RESEARCH, 1998, 39 (01) :34-49
[10]   Development of a multifrequency conductance catheter-based system to determine LV function in mice [J].
Feldman, MD ;
Mao, Y ;
Valvano, JW ;
Pearce, JA ;
Freeman, GL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 279 (03) :H1411-H1420