The effect of Simvastatin treatment on natural antioxidants in low-density lipoproteins and high-energy phosphates and ubiquinone in skeletal muscle

被引:141
作者
Laaksonen, R
Jokelainen, K
Laakso, J
Sahi, T
Harkonen, M
Tikkanen, MJ
Himberg, JJ
机构
[1] UNIV HELSINKI, DEPT MED, ALCOHOL DIS RES UNIT, SF-00250 HELSINKI, FINLAND
[2] UNIV HELSINKI, INST CLIN MED, DEPT CLIN CHEM, SF-00250 HELSINKI, FINLAND
[3] UNIV HELSINKI, DEPT MED, DIV CARDIOL, SF-00250 HELSINKI, FINLAND
[4] HEADQUARTERS FRONTIER GUARD, HELSINKI, FINLAND
[5] MILA LTD, HELSINKI, FINLAND
关键词
D O I
10.1016/S0002-9149(97)89180-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It has been hypothesized that treating hypercholesterolemic patients with statins will lead not only to a reduction in cholesterol, but also to inhibited synthesis of other compounds which derive from the synthetic pathway of cholesterol, In theory, this could further lead to ubiquinone deficiency in muscle cell mitochondria, disturbing normal cellular respiration and causing adverse effects such as rhabdomyolysis. Furthermore, ubiquinone is one of the lipophilic antioxidants in low-density lipoprotein (LDL), and therefore it has also been hypothesized that statin treatment will reduce the antioxidant capacity of LDL, We investigated the effect of 6 months of simvastatin treatment (20 mg/day) on skeletal muscle concentrations of high-energy phosphates and ubiquinone by performing biopsies in 19 hypercholesterolemic patients. Parallel assays were performed in untreated control subjects. The muscle high-energy phosphate and ubiquinone concentrations assayed after simvastatin treatment were similar to those observed at baseline and did nor differ from the values obtained in control subjects at the beginning and end of follow-up. These results do not support the hypothesis of diminished isoprenoid synthesis or energy generation in muscle cells during simvastatin treatment. Furthermore, the results of analysis of antioxidant concentrations in LDL before and after simvastatin treatment indicate that the antioxidant capacity of LDL is maintained in simvastatin-treated patients.
引用
收藏
页码:851 / 854
页数:4
相关论文
共 25 条
[1]   LOVASTATIN INHIBITS LOW-DENSITY-LIPOPROTEIN OXIDATION AND ALTERS ITS FLUIDITY AND UPTAKE BY MACROPHAGES - INVITRO AND INVIVO STUDIES [J].
AVIRAM, M ;
DANKNER, G ;
COGAN, U ;
HOCHGRAF, E ;
BROOK, JG .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (03) :229-235
[2]  
BEYER RE, 1987, CHEM SCRIPTA, V27, P145
[3]   A COMPARISON OF THE EFFECTS OF SIMVASTATIN AND PRAVASTATIN MONOTHERAPY ON MUSCLE HISTOLOGY AND PERMEABILITY IN HYPERCHOLESTEROLEMIC PATIENTS [J].
CONTERMANS, J ;
SMIT, JWA ;
BAR, PR ;
ERKELENS, DW .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1995, 39 (02) :135-141
[4]   SIMULTANEOUS DETERMINATION OF RETINOL AND ALPHA-TOCOPHEROL IN HUMAN-SERUM BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
DELEENHEER, AP ;
DEBEVERE, VORC ;
DERUYTER, MGM ;
CLAEYS, AE .
JOURNAL OF CHROMATOGRAPHY, 1979, 162 (03) :408-413
[5]  
ELMBERGER PG, 1988, J LIPID RES, V29, P1651
[6]  
Feussner Giso, 1994, Current Opinion in Lipidology, V5, P59, DOI 10.1097/00041433-199402000-00010
[7]   LOVASTATIN DECREASES COENZYME-Q LEVELS IN HUMANS [J].
FOLKERS, K ;
LANGSJOEN, P ;
WILLIS, R ;
RICHARDSON, P ;
XIA, LJ ;
YE, CQ ;
TAMAGAWA, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :8931-8934
[8]   REGULATION OF THE MEVALONATE PATHWAY [J].
GOLDSTEIN, JL ;
BROWN, MS .
NATURE, 1990, 343 (6257) :425-430
[9]  
GRINLANDA G, 1993, J CLIN PHARMACOL, V33, P226
[10]  
GRUNDY SM, 1988, NEW ENGL J MED, V319, P24