UBIQUINOL-10 IS AN EFFECTIVE LIPID-SOLUBLE ANTIOXIDANT AT PHYSIOLOGICAL CONCENTRATIONS

被引:547
作者
FREI, B [1 ]
KIM, MC [1 ]
AMES, BN [1 ]
机构
[1] UNIV CALIF BERKELEY,DIV BIOCHEM & MOLEC BIOL,BERKELEY,CA 94720
关键词
Coenzyme Q; Heart disease; Lipid peroxidation; α-tocopherol;
D O I
10.1073/pnas.87.12.4879
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is well known that ubiquinone-10 (coenzyme Q10, ubiquinone 50) acts as an electron carrier of the respiratory chain in mitochondria. In this paper we show that ubiquinol-10, the reduced form of ubiquinone-10, also efficiently scavenges free radicals generated chemically within liposomal membranes. Ubiquinol-10 is about as effective in preventing peroxidative damage to lipids as α-tocopherol, which is considered the best lipid-soluble antioxidant in humans. The number of radicals scavenged by each molecule of ubiquinol-10 is 1.1 under our experimental conditions. In contrast to α-tocopherol, ubiquinol-10 is not recycled by ascorbate. However, it is known that ubiquinol-10 can be recycled by electron transport carriers present in various biomembranes and possibly by some enzymes. We also show that ubiquinol-10 spares α-tocopherol when both antioxidants are present in the same liposomal membranes and that ubiquinol-10, like α-tocopherol, does not interact with reduced glutathione. Our data together with previous work on the antioxidant function of ubiquinol reported in the literature strongly suggest that ubiquinol-10 is an important physiological lipid-soluble antioxidant.
引用
收藏
页码:4879 / 4883
页数:5
相关论文
共 44 条
[31]   MITOCHONDRIA AND MICROSOMAL-MEMBRANES HAVE A FREE-RADICAL REDUCTASE-ACTIVITY THAT PREVENTS CHROMANOXYL RADICAL ACCUMULATION [J].
PACKER, L ;
MAGUIRE, JJ ;
MEHLHORN, RJ ;
SERBINOVA, E ;
KAGAN, VE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 159 (01) :229-235
[32]   DETERMINATION OF ALPHA-TOCOPHEROL AND ALPHA-TOCOPHERYLQUINONE IN SMALL BIOLOGICAL SAMPLES BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH ELECTROCHEMICAL DETECTION [J].
PASCOE, GA ;
DUDA, CT ;
REED, DJ .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1987, 414 (02) :440-448
[33]   ESTIMATION OF THE LOCATION OF NATURAL ALPHA-TOCOPHEROL IN LIPID BILAYERS BY C-13-NMR SPECTROSCOPY [J].
PERLY, B ;
SMITH, ICP ;
HUGHES, L ;
BURTON, GW ;
INGOLD, KU .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 819 (01) :131-135
[34]  
RAMASARMA T, 1985, COENZYME Q BIOCH BIO, P67
[35]   SYNERGISTIC INTERACTION BETWEEN VITAMIN-E AND THE BILE-PIGMENTS BILIRUBIN AND BILIVERDIN [J].
STOCKER, R ;
PETERHANS, E .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1002 (02) :238-244
[36]  
SUGINO K, 1987, SURGERY, V101, P746
[37]  
SUGINO K, 1989, SURGERY, V105, P200
[38]   RECOVERY-TIME COURSE OF VENTRICULAR VULNERABILITY AFTER CORONARY REPERFUSION IN RELATION TO MITOCHONDRIAL-FUNCTION IN ISCHEMIC MYOCARDIUM [J].
SUGIYAMA, S ;
OZAWA, T ;
KATO, T ;
SUZUKI, S .
AMERICAN HEART JOURNAL, 1980, 100 (06) :829-837
[39]   NADH-DEPENDENT AND NADPH-DEPENDENT FORMATION OF SUPEROXIDE ANIONS BY BOVINE HEART SUB-MITOCHONDRIAL PARTICLES AND NADH-UBIQUINONE REDUCTASE PREPARATION [J].
TAKESHIGE, K ;
MINAKAMI, S .
BIOCHEMICAL JOURNAL, 1979, 180 (01) :129-135
[40]  
TAKESHIGE K, 1980, BIOMEDICAL CLIN ASPE, V2, P15