Single Dose Administration of L-Carnitine Improves Antioxidant Activities in Healthy Subjects

被引:45
作者
Cao, Yu [2 ]
Qu, Hai-jun [2 ]
Li, Ping [2 ]
Wang, Chun-bo [3 ]
Wang, Le-xin [1 ]
Han, Zhi-wu [2 ]
机构
[1] Charles Sturt Univ, Sch Biomed Sci, Wagga Wagga, NSW 2678, Australia
[2] Qingdao Univ, Dept Pharm, Affiliated Hosp, Coll Med, Qingdao 266071, Peoples R China
[3] Qingdao Univ, Coll Med, Dept Pharmacol, Qingdao 266071, Peoples R China
关键词
catalase; glutathione peroxidase; L-carnitine; superoxide dismutase; total antioxidative capacity; PERFORMANCE LIQUID-CHROMATOGRAPHY; PLASMA; QUANTIFICATION; DERIVATIZATION; ACYLCARNITINES; TRANSPORT; KINETICS;
D O I
10.1620/tjem.224.209
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
L-carnitine has been used as a supplement to treat cardiovascular or liver disease. However, there has been little information about the effect of L-carnitine on anti-oxidation capability in healthy human subjects. This study was designed to investigate the correlation between plasma L-carnitine concentration and antioxidant activity. Liquid L-carnitine (2.0 g) was administered orally as a single dose in 12 healthy subjects. Plasma concentration of L-carnitine was detected by HPLC. The baseline concentration of L-carnitine was 39.14 +/- 5.65 mu mol/L. After single oral administration, the maximum plasma concentration (C-max) and area under the curve (AUC(0-infinity)) were 84.7 +/- 25.2 mu mol/L and 2,676.4 +/- 708.3 mu mol/L.h, respectively. The half-life and the time required to reach the C-max was 60.3 +/- 15.0 min and 3.4 +/- 0.46 h, respectively. There was a gradual increase in plasma concentrations of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase and total antioxidative capacity (T-AOC) in the first 3.5 h following L-carnitine administration. The plasma concentrations of SOD, GSH-Px, catalase and T-AOC returned to baseline levels within 24 h. A positive correlation was found between L-carnitine concentration and the antioxidant index of SOD (r = 0.992, P < 0.01), GSH-Px (r = 0.932, P < 0.01), catalase (r = 0.972, P < 0.01) or T-AOC (r = 0.934, P < 0.01). In conclusion, L-carnitine increases activities of antioxidant enzymes and the total antioxidant capacity in healthy subjects. It may be useful as a supplementary therapy for chronic illnesses involving excessive oxidative stress.
引用
收藏
页码:209 / 213
页数:5
相关论文
共 22 条
[1]   Comparison of the effects of sodium nitroprusside and L-carnitine in experimental ischemia-reperfusion injury in rats [J].
Akin, M. ;
Kurukahvecioglu, O. ;
Gulbahar, O. ;
Isikgonul, I. ;
Taneri, F. ;
Tezel, E. ;
Onuk, E. .
TRANSPLANTATION PROCEEDINGS, 2007, 39 (10) :2997-3001
[2]   CLINICAL AND BIOCHEMICAL ASPECTS OF CARNITINE DEFICIENCY AND INSUFFICIENCY - TRANSPORT DEFECTS AND INBORN-ERRORS OF BETA-OXIDATION [J].
ANGELINI, C ;
VERGANI, L ;
MARTINUZZI, A .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 1992, 29 (3-4) :217-242
[3]   Disposition and metabolite kinetics of oral L-carnitine in humans [J].
Bain, Marcus A. ;
Milne, Robert W. ;
Evans, Allan M. .
JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 46 (10) :1163-1170
[4]   Insulin action on glucose and protein metabolism during L-carnitine supplementation in maintenance haemodialysis patients [J].
Biolo, Gianni ;
Stulle, Manuela ;
Bianco, Francesco ;
Mengozzi, Giuseppe ;
Barazzoni, Rocco ;
Vasile, Alfonso ;
Panzetta, Giovanni ;
Guarnieri, Gianfranco .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2008, 23 (03) :991-997
[5]   Determination of highly soluble L-carnitine in biological samples by reverse phase high performance liquid chromatography with fluorescent derivatization [J].
Cao, Qing-Ri ;
Ren, Shan ;
Park, Mi-Jin ;
Choi, Yun-Jaie ;
Lee, Beom-Jin .
ARCHIVES OF PHARMACAL RESEARCH, 2007, 30 (08) :1041-1046
[6]   OXYGEN RADICALS AND HUMAN-DISEASE [J].
CROSS, CE ;
HALLIWELL, B ;
BORISH, ET ;
PRYOR, WA ;
AMES, BN ;
SAUL, RL ;
MCCORD, JM ;
HARMAN, D .
ANNALS OF INTERNAL MEDICINE, 1987, 107 (04) :526-545
[7]   Antioxidant and antiradical activities of L-carnitine [J].
Gülçin, I .
LIFE SCIENCES, 2006, 78 (08) :803-811
[8]   FREE-RADICAL INVOLVEMENT IN AGING - PATHOPHYSIOLOGY AND THERAPEUTIC IMPLICATIONS [J].
HARMAN, D .
DRUGS & AGING, 1993, 3 (01) :60-80
[9]  
Irshad M., 2002, Indian Journal of Experimental Biology, V40, P1233
[10]   L-Carnitine transport in human placental brush-border membranes is mediated by the sodium-dependent organic cation transporter OCTN2 [J].
Lahjouji, K ;
Elimrani, I ;
Lafond, J ;
Leduc, L ;
Qureshi, IA ;
Mitchell, GA .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (02) :C263-C269