AMP decreases the efficiency of skeletal-muscle mitochondria

被引:48
作者
Cadenas, S
Buckingham, JA
St-Pierre, J
Dickinson, K
Jones, RB
Brand, MD
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[2] MRC, Dunn Human Nutr Unit, Cambridge CB2 2XY, England
[3] BASF Pharma, Nottingham NG1 1GF, England
[4] Univ Cambridge, Dept Zool, Cambridge CB2 3EJ, England
关键词
adenine nucleotide translocase; nucleotides; proton leak; uncoupling; uncoupling proteins;
D O I
10.1042/0264-6021:3510307
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
Mitochondrial proton leak in rat muscle is responsible for approx. 15 % of the standard metabolic rate, so its modulation could be important in regulating metabolic efficiency. We report in the present paper that physiological concentrations of AMP (K-0.5 = 80 muM) increase the resting respiration rate and double the proton conductance of rat skeletal-muscle mitochondria. This effect is specific for AMP. AMP also doubles proton conductance in skeletal-muscle mitochondria from an ectotherm (the frog Rana temporaria), suggesting that AMP activation is not primarily for thermogenesis, AMP activation in rat muscle mitochondria is unchanged when uncoupling protein-3 is doubled by starvation, indicating that this protein is not involved in the AMP effect. AMP activation is, however, abolished by inhibitors and substrates of the adenine nucleotide translocase (ANT), suggesting that this carrier (possibly the ANT1 isoform) mediates AMP activation. AMP activation of ANT could be important for physiological regulation of metabolic rate.
引用
收藏
页码:307 / 311
页数:5
相关论文
共 40 条
[31]   MITOCHONDRIA FROM BROWN ADIPOSE TISSUE - UNCOUPLING OF OXIDATIVE PHOSPHORYLATION BY LONG CHAIN FATTY ACIDS AND RECOUPLING BY GUANOSINE-TRIPHOSPHATE [J].
RAFAEL, J ;
LUDOLPH, HJ ;
HOHORST, HJ .
HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1969, 350 (09) :1121-&
[32]   O-2 SOLUBILITY IN AQUEOUS-MEDIA DETERMINED BY A KINETIC METHOD [J].
REYNAFARJE, B ;
COSTA, LE ;
LEHNINGER, AL .
ANALYTICAL BIOCHEMISTRY, 1985, 145 (02) :406-418
[33]   Contribution of mitochondrial proton leak to respiration rate in working skeletal muscle and liver and to SMR [J].
Rolfe, DFS ;
Newman, JMB ;
Buckingham, JA ;
Clark, MG ;
Brand, MD .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (03) :C692-C699
[34]   CHARACTERISTICS OF MITOCHONDRIAL PROTON LEAK AND CONTROL OF OXIDATIVE-PHOSPHORYLATION IN THE MAJOR OXYGEN-CONSUMING TISSUES OF THE RAT [J].
ROLFE, DFS ;
HULBERT, AJ ;
BRAND, MD .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1994, 1188 (03) :405-416
[35]   The pH-dependent reciprocal changes in contributions of ADP/ATP antiporter and aspartate/glutamate antiporter to the fatty acid-induced uncoupling [J].
Samartsev, VN ;
Mokhova, EN ;
Skulachev, VP .
FEBS LETTERS, 1997, 412 (01) :179-182
[36]   Uncoupling: new approaches to an old problem of bioenergetics [J].
Skulachev, VP .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1998, 1363 (02) :100-124
[37]   Mitochondrial proton leak and the uncoupling proteins [J].
Stuart, JA ;
Brindle, KM ;
Harper, JA ;
Brand, MD .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1999, 31 (05) :517-525
[38]  
TRAYHURN P, 1987, AM J PHYSIOL, V252, pE236
[39]   INTERACTION OF ADENINE-NUCLEOTIDES WITH THE ADENINE-NUCLEOTIDE TRANSLOCASE REGULATES THE DEVELOPMENTAL-CHANGES IN PROTON CONDUCTANCE OF THE INNER MITOCHONDRIAL-MEMBRANE [J].
VALCARCE, C ;
CUEZVA, JM .
FEBS LETTERS, 1991, 294 (03) :225-228
[40]   MOLECULAR AND PHYSIOLOGICAL ASPECTS OF ADENINE-NUCLEOTIDE TRANSPORT IN MITOCHONDRIA [J].
VIGNAIS, PV .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 456 (01) :1-38