The effect of high-dose simvastatin on free fatty acid metabolism in patients with type 2 diabetes mellitus

被引:26
作者
Isley, WL [1 ]
Harris, WS
Miles, JM
机构
[1] Mayo Clin, Div Endocrinol Nutr & Metab, Endocrine Res Unit, Rochester, MN 55905 USA
[2] Med Amer Heart Inst, St Lukes Lipid & Diabet Res Ctr, Kansas, MI USA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2006年 / 55卷 / 06期
关键词
D O I
10.1016/j.metabol.2006.01.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Statins improve all major lipid fractions, reduce coronary heart disease risk, and may have a minor effect on glucose tolerance. A reduction in free fatty acid flux and concentrations could be partly responsible for these effects. We measured nocturnal and postprandial plasma palmitate concentrations and rate of appearance (R-a) on 2 occasions in 12 obese dyslipidemic subjects with type 2 diabetes mellitus, using a single-blind, crossover format (placebo followed by simvastatin, 80 mg/d), and also on I occasion in 6 untreated control subjects. The diabetic subjects had increased average nocturnal (127 13 vs 80 10 mu mol/L, P <.05) and 2-hour postprandial (49 6 vs 17 2 mu mol/L, P <.001) palmitate concentrations, as well as increased nocturnal (31.6 +/- 3.7 vs 19.5 +/- 3.7 mmol/m(2) over 9 hours, P <.05) and postprandial (11.5 +/- 3.7 vs 5.5 +/- 3.7 mmol/m(2) over 4 hours, P <.005) integrated palmitate Ra compared to normal controls. High-dose simvastatin reduced serum triglycerides by 35% but had no effect on plasma palmitate concentrations or R-a. These results suggest that the triglyceride-lowering effect of statins is not mediated through an effect on FFA metabolism. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:758 / 762
页数:5
相关论文
共 36 条
[1]  
Berkplanken I, 2001, DIABETES CARE, V24, P1335
[2]  
Collins R, 2003, LANCET, V361, P2005
[3]  
COPPACK SW, 1994, J LIPID RES, V35, P177
[4]   A comparison of the effects of fluvastatin and bezafibrate on exercise metabolism: A placebo-controlled study in healthy normolipidaemic subjects [J].
Eagles, CJ ;
Kendall, MJ ;
Maxwell, S .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 41 (05) :381-387
[5]  
Freeman DJ, 2001, CIRCULATION, V103, P357
[6]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[7]   Reduction in hepatic non-esterified fatty acid concentration after long-term treatment with atorvastatin lowers hepatic triglyceride synthesis and its secretion in sucrose-fed rats [J].
Funatsu, T ;
Goto, M ;
Kakuta, H ;
Suzuki, M ;
Ida, M ;
Nishijima, S ;
Tanaka, H ;
Yasuda, S ;
Miyata, K .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1580 (2-3) :161-170
[8]   Prolonged inhibition of cholesterol synthesis by atorvastatin inhibits apo B-100 and triglyceride secretion from HepG2 cells [J].
Funatsu, T ;
Suzuki, K ;
Goto, M ;
Arai, Y ;
Kakuta, H ;
Tanaka, H ;
Yasuda, S ;
Ida, M ;
Nishijima, S ;
Miyata, K .
ATHEROSCLEROSIS, 2001, 157 (01) :107-115
[9]   LIPOPROTEIN PHYSIOLOGY IN NONDIABETIC AND DIABETIC STATES - RELATIONSHIP TO ATHEROGENESIS [J].
GINSBERG, HN .
DIABETES CARE, 1991, 14 (09) :839-855
[10]   SPLANCHNIC METABOLISM OF FREE FATTY ACIDS AND PRODUCTION OF TRIGLYCERIDES OF VERY LOW DENSITY LIPOPROTEINS IN NORMOTRIGLYCERIDEMIC AND HYPERTRIGLYCERIDEMIC HUMANS [J].
HAVEL, RJ ;
KANE, JP ;
BALASSE, EO ;
SEGEL, N ;
BASSO, LV .
JOURNAL OF CLINICAL INVESTIGATION, 1970, 49 (11) :2017-&