An improved isolated, left ventricular ejecting, murine heart model - Functional and metabolic evaluation

被引:20
作者
De Windt, LJ
Willems, J
Reneman, RS
Van der Vusse, GJ
Arts, T
Van Bilsen, M
机构
[1] Maastricht Univ, Inst Cardiovasc Res, Dept Physiol, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Cardiovasc Res Inst, Dept Biophys, NL-6200 MD Maastricht, Netherlands
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1999年 / 437卷 / 02期
关键词
isolated murine heart; antegrade perfusion; functional stability; high-energy phosphates;
D O I
10.1007/s004240050767
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
An improved, isolated, left ventricular-ejecting, murine heart model is described and evaluated. Special attention was paid to the design and impedance characteristics of the artificial aortic outflow tract and perfusate composition, which contained glucose (10 mM plus insulin) and pyruvate (1.5 mM) as substrates. Temperature of the isolated perfused hearts was maintained at 38.5 degrees C. During antegrade perfusion (preload 10 mm Hg, afterload 50 mm Hg, 2.5 mM Ca2+) proper design of the aortic outflow tract provided baseline values for cardiac output (CO), left ventricular developed pressure (LVDP) and the maximum first derivative of left ventricular pressure (LV dP/dt(max)) of 11.1 +/- 1.7 ml min(-1), 83 +/- 5 mm Hg and 6283 +/- 552 mm Hg s(-1), respectively, resembling findings in the intact mouse. During 100 min normoxic antegrade perfusion CO declined non-significantly by less than 10%. Varying pre- and afterloads resulted in typical Frank-Starling relationships with maximal CO values of 18.6 +/- 1.8 ml min(-1) at pre- and afterload pressures of 25 and 50 mm Hg, respectively Left ventricular function curves were constructed at free [Ca2+] of 1.5 and 2.5 mM in the perfusion medium. Significantly higher values for CO, LVDP and LV dP/dt(max) and LV dP/dt(max) were obtained at 2.5 mM Ca2+ at all loading conditions investigated. Phosphocreatine and creatine levels remained stable throughout the perfusion period. Despite a small but significant decline in tissue ATP content, the sum of adenine nucleotides did not change during the normoxic perfusion period. The tissue content of glycogen increased significantly.
引用
收藏
页码:182 / 190
页数:9
相关论文
共 32 条
  • [1] IMPROVED AUTOMATED LACTATE DETERMINATION
    APSTEIN, CS
    PUCHNER, E
    BRACHFELD, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1970, 38 (01) : 20 - +
  • [2] MICROSPHERE AND DILUTION TECHNIQUES FOR THE DETERMINATION OF BLOOD FLOWS AND VOLUMES IN CONSCIOUS MICE
    BARBEE, RW
    PERRY, BD
    RE, RN
    MURGO, JP
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (03): : R728 - R733
  • [3] BERGMEYER H.U., 1974, METHODS ENZYMATIC AN, P574, DOI DOI 10.1016/B978-0-12-091302-2.50010-4
  • [4] A work-performing heart preparation for myocardial performance analysis in murine hearts
    Bittner, HB
    Chen, EP
    Peterseim, DS
    VanTrigt, P
    [J]. JOURNAL OF SURGICAL RESEARCH, 1996, 64 (01) : 57 - 62
  • [5] Genes and physiology: Molecular physiology in genetically engineered animals
    Chien, KR
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (04) : 901 - 909
  • [6] CONROY PJ, 1980, J PHARMACOL EXP THER, V212, P47
  • [7] SUBSTRATE-INDUCED CHANGES IN THE LIPID-CONTENT OF ISCHEMIC AND REPERFUSED MYOCARDIUM - ITS RELATION TO HEMODYNAMIC RECOVERY
    DEGROOT, MJM
    COUMANS, WA
    WILLEMSEN, PHM
    VANDERVUSSE, GJ
    [J]. CIRCULATION RESEARCH, 1993, 72 (01) : 176 - 186
  • [8] Transgenic animal models: New avenues in cardiovascular physiology
    Franz, WM
    Mueller, OJ
    Hartong, R
    Frey, N
    Katus, HA
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 1997, 75 (02): : 115 - 129
  • [9] Myocardial function in the working mouse heart overexpressing cardiac A1 adenosine receptors
    Gauthier, NS
    Headrick, JP
    Matherne, GP
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1998, 30 (01) : 187 - 193
  • [10] Determination of function in the isolated working mouse heart: Issues in experimental design
    Gauthier, NS
    Matherne, GP
    Morrison, RR
    Headrick, TP
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1998, 30 (03) : 453 - 461