Coenzyme Q10 supplementation reduces oxidative stress and increases antioxidant enzyme activity in patients with coronary artery disease

被引:108
作者
Lee, Bor-Jen [1 ,2 ]
Huang, Yi-Chia [1 ,3 ]
Chen, Shu-Ju [4 ]
Lin, Ping-Ting [1 ,3 ]
机构
[1] Chung Shan Med Univ, Sch Nutr, Taichung, Taiwan
[2] Taichung Vet Gen Hosp, Intens Care Unit, Taichung, Taiwan
[3] Chung Shan Med Univ Hosp, Dept Nutr, Taichung, Taiwan
[4] Chung Chou Inst Technol Changhua, Dept Nutr & Hlth Sci, Changhua, Taiwan
关键词
Coenzyme Q10; Lipid peroxidation; Antioxidant enzyme activity; Supplementation; Coronary artery disease; Placebo-controlled study; LIPID-PEROXIDATION; DOUBLE-BLIND; HEART-DISEASE; Q(10); PLASMA; UBIQUINOL-10; HOMOCYSTEINE; DEFICIENCY; ANGINA; TISSUE;
D O I
10.1016/j.nut.2011.06.004
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objective: The purpose of this study was to investigate the effect of coenzyme Q10 supplementation on oxidative stress and antioxidant enzyme activity in patients with coronary artery disease (CAD). Methods: This was an intervention study. Patients who were identified by cardiac catheterization as having at least 50% stenosis of one major coronary artery or receiving percutaneous transluminal coronary angioplasty (n = 51) were randomly assigned to the placebo group (n = 14) or one of the two coenzyme Q10-supplemented groups (60 mg/d, n = 19 [Q10-60 group]; 150 mg/d, n = 18 [Q10-150 group]). Intervention was administered for 12 wk. Patients' blood samples were analyzed every 4 wk for plasma coenzyme Q10 concentrations, malondialdehyde (MDA), and antioxidant enzyme (catalase [CAT], superoxide dismutase [SOD], glutathione peroxidase) activity. Results: Forty-three subjects with CAD completed intervention study. Plasma coenzyme Q10 concentration increased significantly after coenzyme the Q10-150 intervention (P < 0.01). The MDA levels were significantly lower than baseline in the Q10-150 group at week 4 (P = 0.03). The Q10-150 group had significantly lower MDA levels than the placebo group at week 8 (P = 0.03). With respect to antioxidant enzyme activity, subjects in the Q10-150 group had significantly higher CAT (P = 0.03) and SOD (P = 0.03) activity than the placebo group at week 12. The plasma coenzyme Q10 concentration was significantly correlated with MDA levels (r = -0.35, P = 0.02) and CAT (r = 0.43, P = 0.01) and SOD activity (r = 0.39, P = 0.01). The ratio of plasma coenzyme Q10 to total cholesterol was significantly correlated with SOD activity (r = 0.39, P = 0.02). The ratio of plasma coenzyme Q10 to low-density lipoprotein was significantly correlated with CAT (r = 0.35, P = 0.04) and SOD (r = 0.45, P = 0.01) activity. However, there was no relation between coenzyme Q10 concentration and glutathione peroxidase activity. Conclusion: Coenzyme Q10 supplements at a dose of 150 mg can decrease oxidative stress and increase antioxidant enzyme activity in patients with CAD. A higher dose of coenzyme Q10 supplements (> 150 mg/d) might promote rapid and sustainable antioxidation in patients with CAD. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:250 / 255
页数:6
相关论文
共 43 条
[31]  
MAZZOLA C, 1987, CURR THER RES CLIN E, V41, P923
[32]   Concentration response to the coenzyme Q10 supplement Q-Gel in human volunteers [J].
Molyneux, Sarah ;
Florkowski, Christopher ;
McGrane, Yasmin ;
Lever, Michael ;
George, Peter .
NUTRITION RESEARCH, 2007, 27 (06) :307-312
[33]  
Mortensen SA, 1997, MOL ASPECTS MED, V18, pS137
[34]   Coenzyme Q10 in cardiovascular disease [J].
Pepe, Salvatore ;
Marasco, Silvana F. ;
Haas, Steven J. ;
Sheeran, Freya L. ;
Krum, Henry ;
Rosenfeldt, Franklin L. .
MITOCHONDRION, 2007, 7 :S154-S167
[35]   UBIQUINONE (COENZYME-Q10) IN THE LONG-TERM TREATMENT OF IDIOPATHIC DILATED CARDIOMYOPATHY [J].
PERMANETTER, B ;
ROSSY, W ;
KLEIN, G ;
WEINGARTNER, F ;
SEIDL, KF ;
BLOMER, H .
EUROPEAN HEART JOURNAL, 1992, 13 (11) :1528-1533
[36]  
Sarter Barbara, 2002, J Cardiovasc Nurs, V16, P9
[37]  
SINGH RB, 1994, ACTA CARDIOL, V49, P441
[38]   Randomized, double-blind placebo-controlled trial of coenzyme Q10 in patients with acute myocardial infarction [J].
Singh, RB ;
Wander, GS ;
Rastogi, A ;
Shukla, PK ;
Mittal, A ;
Sharma, JP ;
Mehrotra, SK ;
Kapoor, R ;
Chopra, RK .
CARDIOVASCULAR DRUGS AND THERAPY, 1998, 12 (04) :347-353
[39]  
Singh U, 2007, NUTR REV, V65, P286, DOI [10.1301/nr.2007.jun.286-293, 10.1111/j.1753-4887.2007.tb00306.x]
[40]   UBIQUINOL-10 PROTECTS HUMAN LOW-DENSITY-LIPOPROTEIN MORE EFFICIENTLY AGAINST LIPID-PEROXIDATION THAN DOES ALPHA-TOCOPHEROL [J].
STOCKER, R ;
BOWRY, VW ;
FREI, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1646-1650