Functional coupling as a basic mechanism of feedback regulation of cardiac energy metabolism

被引:60
作者
Saks, VA
Kuznetsov, AV
Vendelin, M
Guerrero, K
Kay, L
Seppet, EK
机构
[1] Univ Grenoble 1, INSERM E0221, Lab Fundamental & Appl Bioenerget, Struct & Quantitat Bioenerget Res Grp, Grenoble, France
[2] NICPB, Lab Bioenerget, Tallinn, Estonia
[3] Univ Innsbruck Hosp, Dept Transplant Surg, A-6020 Innsbruck, Austria
[4] Estonian Acad Sci, Inst Cybernet, Tallinn, Estonia
[5] Univ Tartu, Dept Pathophysiol, Tartu, Estonia
关键词
heart; skeletal muscle; mitochondria; respiration; regulation; mathematical modelling;
D O I
10.1023/B:MCBI.0000009868.92189.fb
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In this review we analyze the concepts and the experimental data on the mechanisms of the regulation of energy metabolism in muscle cells. Muscular energetics is based on the force - length relationship, which in the whole heart is expressed as a Frank Starling law, by which the alterations of left ventricle diastolic volume change linearly both the cardiac work and oxygen consumption. The second basic characteristics of the heart is the metabolic stability - almost constant levels of high energy phosphates, ATP and phosphocreatine, which are practically independent of the workload and the rate of oxygen consumption, in contrast to the fast-twitch skeletal muscle with no metabolic stability and rapid fatigue. Analysis of the literature shows that an increase in the rate of oxygen consumption by order of magnitude, due to Frank - Starling law, is observed without any significant changes in the intracellular calcium transients. Therefore, parallel activation of contraction and mitochondrial respiration by calcium ions may play only a minor role in regulation of respiration in the cells. The effective regulation of the respiration under the effect of Frank - Starling law and metabolic stability of the heart are explained by the mechanisms of functional coupling within supramolecular complexes in mitochondria, and at the subcellular level within the intracellular energetic units. Such a complex structural and functional organisation of heart energy metabolism can be described quantitatively by mathematical models.
引用
收藏
页码:185 / 199
页数:15
相关论文
共 93 条
[1]   Compartmentalized energy transfer in cardiomyocytes: Use of mathematical modeling for analysis of in vivo regulation of respiration [J].
Aliev, MK ;
Saks, VA .
BIOPHYSICAL JOURNAL, 1997, 73 (01) :428-445
[2]   THE CELLULAR BASIS OF THE LENGTH TENSION RELATION IN CARDIAC-MUSCLE [J].
ALLEN, DG ;
KENTISH, JC .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1985, 17 (09) :821-840
[3]   Possible role of cytoskeleton in intracellular arrangement and regulation of mitochondria [J].
Appaix, F ;
Kuznetsov, AV ;
Usson, Y ;
Kay, L ;
Andrienko, T ;
Olivares, J ;
Kaambre, T ;
Sikk, P ;
Margreiter, R ;
Saks, V .
EXPERIMENTAL PHYSIOLOGY, 2003, 88 (01) :175-190
[4]   A method for the study of the perfused pancreas. [J].
Babkin, BP ;
Starling, EH .
JOURNAL OF PHYSIOLOGY-LONDON, 1926, 61 (02) :245-247
[5]   Cardiac energy metabolism homeostasis: Role of cytosolic calcium [J].
Balaban, RS .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2002, 34 (10) :1259-1271
[6]   RELATION BETWEEN WORK AND PHOSPHATE METABOLITE IN THE INVIVO PACED MAMMALIAN HEART [J].
BALABAN, RS ;
KANTOR, HL ;
KATZ, LA ;
BRIGGS, RW .
SCIENCE, 1986, 232 (4754) :1121-1123
[7]  
BARBOUR RL, 1984, J BIOL CHEM, V259, P8246
[8]  
Bers D.M., 2001, Excitation-Contraction Coupling and Cardiac Contractile Force, V2th
[9]   Alteration of mitochondrial function in a model of chronic ischemia in vivo in rat heart [J].
Boudina, S ;
Laclau, MN ;
Tariosse, L ;
Daret, D ;
Gouverneur, G ;
Bonoron-Adèle, S ;
Saks, VA ;
Dos Santos, P .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 282 (03) :H821-H831
[10]   Regulation of mitochondrial [NADH] by cytosolic [Ca2+] and work in trabeculae from hypertrophic and normal rat hearts [J].
Brandes, R ;
Maier, LS ;
Bers, DM .
CIRCULATION RESEARCH, 1998, 82 (11) :1189-1198