Effect of gemfibrozil on serum levels of prostacyclin and precursor fatty acids in hyperlipidemic patients with type 2 diabetes

被引:14
作者
Yoshinari, M [1 ]
Asano, T [1 ]
Kaori, S [1 ]
Shi, AH [1 ]
Wakisaka, M [1 ]
Iwase, M [1 ]
Fujishima, M [1 ]
机构
[1] Kyushu Univ, Fac Med, Dept Internal Med 2, Fukuoka 8128582, Japan
关键词
gemtibrozil; prostacyclin; fatty acids; type 2 diabetes mellitus;
D O I
10.1016/S0168-8227(98)00107-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lipid-lowering fibrate drugs are known to affect the synthesis of fatty acids, which may alter the prostacyclin synthesis in diabetic patients. Therefore, the serum levels of precursor fatty acids and 6-keto-prostaglandin F-1 alpha (6-keto PGF(1 alpha)) were determined in ten hyperlipidemic patients with Type 2 diabetes before and after administration of gemfibrozil (900 mg/day) for 3 months, in comparison with the results in seven non-diabetic hyperlipidemic patients. Gemfibrozil significantly reduced the serum concentration of dihomo-gamma-linolenic acid, total cholesterol and triglycerides, but did not affect the serum levels of arachidonic acid and 6-keto PGF(1 alpha) in diabetic and non-diabetic patients. Thus, gemfibrozil did not affect the synthesis of prostacyclin in spite of the reduction of precursor fatty acids in diabetic and non-diabetic patients. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:149 / 154
页数:6
相关论文
共 20 条
[1]   SELECTIVE MODIFICATION OF RAT HEPATIC-MICROSOMAL FATTY-ACID CHAIN ELONGATION AND DESATURATION BY FIBRATES - RELATIONSHIP WITH PEROXISOME PROLIFERATION [J].
ALEGRET, M ;
CERQUEDA, E ;
FERRANDO, R ;
VAZQUEZ, M ;
SANCHEZ, RM ;
ADZET, T ;
MERLOS, M ;
LAGUNA, JC .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 114 (07) :1351-1358
[2]  
ALLAIN CC, 1974, CLIN CHEM, V20, P470
[3]  
ALLEN JK, 1979, CLIN CHEM, V25, P325
[4]  
BANAUCH D, 1975, Z KLIN CHEM KLIN BIO, V13, P101
[5]   COMPARISON OF GEMFIBROZIL VERSUS SIMVASTATIN IN FAMILIAL COMBINED HYPERLIPIDEMIA AND EFFECTS ON APOLIPOPROTEIN-B-CONTAINING LIPOPROTEINS, LOW-DENSITY-LIPOPROTEIN SUBFRACTION PROFILE, AND LOW-DENSITY-LIPOPROTEIN OXIDIZABILITY [J].
BREDIE, SJH ;
DEBRUIN, TWA ;
DEMACKER, PNM ;
KASTELEIN, JJP ;
STALENHOEF, AFH .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (05) :348-353
[6]   PROSTACYCLIN RELEASE FROM THE HUMAN SAPHENOUS-VEIN IN DIABETICS IS LOWER THAN IN NONDIABETICS [J].
BRUNKWALL, JS ;
BERGQVIST, D .
WORLD JOURNAL OF SURGERY, 1992, 16 (06) :1141-1146
[7]   RAPID METHOD FOR DETERMINATION OF GLYCOSYLATED HEMOGLOBINS USING HIGH-PRESSURE LIQUID-CHROMATOGRAPHY [J].
COLE, RA ;
SOELDNER, JS ;
DUNN, PJ ;
BUNN, HF .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1978, 27 (03) :289-301
[8]   ESSENTIAL FATTY-ACID METABOLISM IN PATIENTS WITH ESSENTIAL-HYPERTENSION, DIABETES-MELLITUS AND CORONARY HEART-DISEASE [J].
DAS, UN .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1995, 52 (06) :387-391
[9]   REEVALUATION OF CIRCULATING PROSTACYCLIN AND THROMBOXANE IN DIABETES [J].
KAZAMA, Y ;
KANEMARU, Y ;
NOGUCHI, T ;
ONAYA, T .
PROSTAGLANDINS LEUKOTRIENES AND MEDICINE, 1987, 26 (02) :115-122
[10]   α- and β-alkyl-substituted eicosapentaenoic acids -: Incorporation into phospholipids and effects on prostaglandin H synthase and 5-lipoxygenase [J].
Larsen, LN ;
Bremen, J ;
Flock, S ;
Skattebol, L .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (04) :405-411