PROPORTIONAL ACTIVATION COEFFICIENTS DURING STIMULATION OF OXIDATIVE-PHOSPHORYLATION BY LACTATE AND PYRUVATE OR BY VASOPRESSIN

被引:49
作者
KORZENIEWSKI, B [1 ]
HARPER, ME [1 ]
BRAND, MD [1 ]
机构
[1] JAGIELLONIAN UNIV, INST MOLEC BIOL, PL-31120 KRAKOW, POLAND
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 1995年 / 1229卷 / 03期
基金
加拿大自然科学与工程研究理事会;
关键词
OXIDATIVE PHOSPHORYLATION; PROPORTIONAL ACTIVATION; CALCIUM ACTING HORMONE; GLUCONEOGENESIS; LACTATE; PYRUVATE;
D O I
10.1016/0005-2728(95)00008-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A 'proportional activation' approach designed to deal with the influence of external effecters within biochemical systems is described. The proportional activation coefficient, which enables the quantitative determination of the relative stimulation of different parts of a system by a given effector, is defined. The proportional activation approach was used to calculate the relative activation of Delta p-producing and Delta p-consuming subsystems during stimulation of the respiration rate of cells by a variety of different effecters. Oxidative phosphorylation was stimulated by the addition of either lactate and pyruvate (10 mM and 1 mM) or vasopressin. The addition of lactate and pyruvate to suspensions of resting hepatocytes increased the respiration rate by about 50%. The Delta p-consuming subsystem was stimulated about 60% as much as the Delta p-producing subsystem. Quinolinic acid, commonly considered to be a specific inhibitor of gluconeogenesis, was found to block the Delta p-producing oxidative subsystem as well as the Delta p-consuming subsystem, indicating some nonspecific effects of this inhibitor. Addition of vasopressin to hepatocytes that were incubated in the presence of lactate and pyruvate resulted in an increase of the respiratory rate by up to 35%. The relative stimulation of the Delta p-producing and Delta p-consuming subsystems was essentially equal. Using the 'proportional activation approach' to analyse these and previously published data, it is shown that substrates (lactate/pyruvate and fatty acids), Ca2+-acting hormones (vasopressin and others) and calcium in muscles (heart muscle and skeletal muscle) activate both subsystems to a similar extent (it concerns especially Ca2+-dependent systems).
引用
收藏
页码:315 / 322
页数:8
相关论文
共 37 条
[21]   EFFECTS OF GLUCAGON ON THE REDOX STATES OF CYTOCHROMES IN MITOCHONDRIA INSITU IN PERFUSED-RAT-LIVER [J].
KIMURA, S ;
SUZAKI, T ;
KOBAYASHI, S ;
ABE, K ;
OGATA, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 119 (01) :212-219
[22]   AN EXTENDED DYNAMIC-MODEL OF OXIDATIVE-PHOSPHORYLATION [J].
KORZENIEWSKI, B ;
FRONCISZ, W .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1060 (02) :210-223
[23]   THEORETICAL-STUDIES ON THE CONTROL OF THE OXIDATIVE-PHOSPHORYLATION SYSTEM [J].
KORZENIEWSKI, B ;
FRONCISZ, W .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1102 (01) :67-75
[24]  
LANOUE KF, 1972, J BIOL CHEM, V247, P667
[25]  
Martin BR, 1987, METABOLIC REGULATION
[26]   THE ROLE OF MITOCHONDRIAL-CA2+ TRANSPORT AND MATRIX-CA2+ IN SIGNAL TRANSDUCTION IN MAMMALIAN-TISSUES [J].
MCCORMACK, JG ;
DENTON, RM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1018 (2-3) :287-291
[27]  
MCMILLIN JB, 1988, MOL CELL BIOCHEM, V81, P121
[28]   INFLUENCE OF NAD-LINKED DEHYDROGENASE-ACTIVITY ON FLUX THROUGH OXIDATIVE-PHOSPHORYLATION [J].
MORENOSANCHEZ, R ;
HOGUE, BA ;
HANSFORD, RG .
BIOCHEMICAL JOURNAL, 1990, 268 (02) :421-428
[29]  
NOBES CD, 1990, J BIOL CHEM, V265, P12910
[30]   MEASUREMENT OF THE INTRAMITOCHONDRIAL VOLUME IN HEPATOCYTES WITHOUT CELL DISRUPTION AND ITS ELEVATION BY HORMONES AND VALINOMYCIN [J].
QUINLAN, PT ;
THOMAS, AP ;
ARMSTON, AE ;
HALESTRAP, AP .
BIOCHEMICAL JOURNAL, 1983, 214 (02) :395-404