Plasma lipoprotein composition and cholesteryl ester transfer from high density lipoproteins to very low density and low density lipoproteins in patients with non-insulin-dependent diabetes mellitus

被引:0
作者
Bhatnagar, D
Durrington, PN
Kumar, S
Mackness, MI
Boulton, AJM
机构
关键词
cholesteryl ester; cholesteryl ester transfer; CETP; LCAT; lipoproteins; NIDDM;
D O I
10.1002/(SICI)1096-9136(199602)13:2<139::AID-DIA15>3.3.CO;2-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have examined cholesteryl ester transfer (GET) from HDL to low density and very low density lipoproteins (LDL and VLDL) and lecithin:cholesterol acyl transferase (LCAT) activity in plasma from 28 men with non-insulin-dependent diabetes mellitus (NIDDM) treated with diet alone or diet and sulphonylurea drugs and in 27 healthy non-diabetic controls. Patients and healthy subjects had similar LCAT activity, but CET was significantly higher in NIDDM 26.1 +/- 11.5 mu mol l(-1) h(-1)) than in healthy men (17.8 +/- 6.5 mu mol l(-1) h(-1)) (p = 0.001). Diabetic men also had higher CET compared to 15 healthy non-diabetic men (18.7 +/- 5.6 mu mol l(-1) h(-1)) (p = 0.001) with similar serum lipids. CET activity was similar in patients treated with diet alone (24.8 +/- mu mol l(-1) h(-1)) or with sulphonylureas (27.7 +/- 15.8 mu mol l(-1) h(-1)). The Sf 0-12 fraction was significantly enriched with total cholesterol (p = 0.0001) and free cholesterol (p = 0.006) in diabetic subjects whether treated with diet alone or on sulphonylureas compared to the 15 non-diabetic controls matched for serum triglycerides. The free cholesterol/phospholipid, the free cholesterol/total protein and the free cholesterol/mass ratios were increased in the Sf 0-12 fraction in diabetic subjects (p < 0.01). These findings indicate that CET is accelerated in patients with NIDDM and that this may be due to the altered composition of acceptor lipoproteins.
引用
收藏
页码:139 / 144
页数:6
相关论文
共 36 条
[1]   DECREASED ABILITY OF HIGH-DENSITY-LIPOPROTEINS TO TRANSFER CHOLESTEROL ESTERS IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
AHNADI, CE ;
MASMOUDI, T ;
BERTHEZENE, F ;
PONSIN, G .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1993, 23 (08) :459-465
[2]   ACCELERATED CHOLESTERYL ESTER TRANSFER IN NONINSULIN-DEPENDENT DIABETES-MELLITUS [J].
BAGDADE, JD ;
LANE, JT ;
SUBBAIAH, PV ;
OTTO, ME ;
RITTER, MC .
ATHEROSCLEROSIS, 1993, 104 (1-2) :69-77
[3]   ACCELERATED CHOLESTERYL ESTER TRANSFER IN PLASMA OF PATIENTS WITH HYPERCHOLESTEROLEMIA [J].
BAGDADE, JD ;
RITTER, MC ;
SUBBAIAH, PV .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (04) :1259-1265
[4]   PERSISTENT ABNORMALITIES IN LIPOPROTEIN COMPOSITION IN NONINSULIN-DEPENDENT DIABETES AFTER INTENSIVE INSULIN THERAPY [J].
BAGDADE, JD ;
BUCHANAN, WE ;
KUUSI, T ;
TASKINEN, MR .
ARTERIOSCLEROSIS, 1990, 10 (02) :232-239
[5]  
BARTER PJ, 1990, CURR OPIN LIPIDOL, V1, P518
[6]   INCREASED TRANSFER OF CHOLESTERYL ESTERS FROM HIGH-DENSITY-LIPOPROTEINS TO LOW-DENSITY AND VERY LOW-DENSITY LIPOPROTEINS IN PATIENTS WITH ANGIOGRAPHIC EVIDENCE OF CORONARY-ARTERY DISEASE [J].
BHATNAGAR, D ;
DURRINGTON, PN ;
CHANNON, KM ;
PRAIS, H ;
MACKNESS, MI .
ATHEROSCLEROSIS, 1993, 98 (01) :25-32
[7]   EFFECTS OF TREATMENT OF HYPERTRIGLYCERIDEMIA WITH GEMFIBROZIL ON SERUM-LIPOPROTEINS AND THE TRANSFER OF CHOLESTERYL ESTER FROM HIGH-DENSITY-LIPOPROTEINS TO LOW-DENSITY LIPOPROTEINS [J].
BHATNAGAR, D ;
DURRINGTON, PN ;
MACKNESS, MI ;
ARROL, S ;
WINOCOUR, PH ;
PRAIS, H .
ATHEROSCLEROSIS, 1992, 92 (01) :49-57
[8]  
BROWN MS, 1986, SCIENCE, V47, P232
[9]   INVESTIGATION OF LIPID TRANSFER IN HUMAN-SERUM LEADING TO THE DEVELOPMENT OF AN ISOTOPIC METHOD FOR THE DETERMINATION OF ENDOGENOUS CHOLESTEROL ESTERIFICATION AND TRANSFER [J].
CHANNON, KM ;
CLEGG, RJ ;
BHATNAGAR, D ;
ISHOLA, M ;
ARROL, S ;
DURRINGTON, PN .
ATHEROSCLEROSIS, 1990, 80 (03) :217-226
[10]   INCREASED FREE-CHOLESTEROL IN PLASMA LOW AND VERY LOW-DENSITY LIPOPROTEINS IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS - ITS ROLE IN THE INHIBITION OF CHOLESTERYL ESTER TRANSFER [J].
FIELDING, CJ ;
REAVEN, GM ;
LIU, G ;
FIELDING, PE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (08) :2512-2516