Impaired cardiac mitochondrial membrane potential and respiration in copper-deficient rats

被引:32
作者
Chen, XL [1 ]
Jennings, DB [1 ]
Medeiros, DM [1 ]
机构
[1] Kansas State Univ, Dept Human Nutr, Manhattan, KS 66506 USA
关键词
copper deficiency; mitochondria; ATP synthase; oligomycin; membrane potential; heart;
D O I
10.1023/A:1021258204921
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
Cardiac mitochondrial respiration, ATP synthase activity, and membrane potential and intactness were evaluated in copper-deficient rats. In the presence of NADH, both copper-deficient and copper-adequate mitochondria had very low oxygen consumption rates, indicating membrane intactness. However copper-deficient mitochondria had significantly lower oxygen consumption rates with NADH than did copper-adequate mitochondria. Copper-deficient mitochondria had significantly lower membrane potential than did copper-adequate mitochondria using fluorescent dyes. Copper-deficient mitochondria had significantly lower state 3 oxygen consumption rates and were less sensitive to inhibition by oligomycin, an ATP synthase inhibitor. Copper-deficient and copper-adequate mitochondria responded similiarly to CCCP. No difference was observed in mitochondrial ATPase activity between copper-deficient and copper-adequate rats using submitochondrial particles. We conclude that cardiac mitochondrial respiration is compromised in copper-deficient rats, and may be related to an altered ATP synthase complex and/or a decreased mitochondrial membrane potential.
引用
收藏
页码:397 / 406
页数:10
相关论文
共 18 条
[1]
CATTERALL WA, 1971, J BIOL CHEM, V246, P4987
[2]
CHAO JC, 1993, COMP BIOCH PHYSL, V104, P103
[3]
LOW-LEVELS OF ATP SYNTHASE AND CYTOCHROME-C-OXIDASE SUBUNIT PEPTIDE FROM HEARTS OF COPPER-DEFICIENT RATS ARE NOT ALTERED BY THE ADMINISTRATION OF DIMETHYL-SULFOXIDE [J].
CHAO, JCJ ;
MEDEIROS, DM ;
DAVIDSON, J ;
SHIRY, L .
JOURNAL OF NUTRITION, 1994, 124 (06) :789-803
[4]
The oligomycin sensitivity conferring protein of rat liver mitochondrial ATP synthase:: Arginine 94 is important for the binding of OSCP to F1 [J].
Golden, TR ;
Pedersen, PL .
BIOCHEMISTRY, 1998, 37 (39) :13871-13881
[5]
LOCALIZATION OF MITOCHONDRIA IN LIVING CELLS WITH RHODAMINE-123 [J].
JOHNSON, LV ;
WALSH, ML ;
CHEN, LB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (02) :990-994
[6]
Lisa F.Di., 1995, J PHYSL, V486, P1, DOI [10.1113/jphysiol.1995.sp020786, DOI 10.1113/JPHYSIOL.1995.SP020786]
[7]
Mitochondrial transcription factor A is increased but expression of ATP synthase β subunit and medium-chain acyl-CoA dehydrogenase genes are decreased in hearts of copper-deficient rats [J].
Mao, SM ;
Leone, TC ;
Kelly, DP ;
Medeiros, DM .
JOURNAL OF NUTRITION, 2000, 130 (09) :2143-2150
[8]
MARKLUND S, 1974, European Journal of Biochemistry, V47, P469, DOI 10.1111/j.1432-1033.1974.tb03714.x
[9]
FUNCTIONAL-ASPECTS OF OXIDATIVE-PHOSPHORYLATION AND ELECTRON-TRANSPORT IN CARDIAC MITOCHONDRIA OF COPPER-DEFICIENT RATS [J].
MATZ, JM ;
SAARI, JT ;
BODE, AM .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1995, 6 (12) :644-652
[10]
COPPER DEFICIENCY IN A GENETICALLY HYPERTENSIVE CARDIOMYOPATHIC RAT - ELECTROCARDIOGRAM, FUNCTIONAL AND ULTRASTRUCTURAL ASPECTS [J].
MEDEIROS, DM ;
LIAO, ZM ;
HAMLIN, RL .
JOURNAL OF NUTRITION, 1991, 121 (07) :1026-1034