Effect of thiazolidinediones on glucose and fatty acid metabolism in patients with type 2 diabetes

被引:105
作者
Boden, G
Cheung, P
Mozzoli, M
Fried, SK
机构
[1] Rutgers State Univ, Dept Nutrit Sci, New Brunswick, NJ 08903 USA
[2] Temple Univ, Sch Med, Gen Clin Res Ctr, Philadelphia, PA 19122 USA
[3] Temple Univ, Sch Med, Div Endocrinol Diabet Metab, Philadelphia, PA 19122 USA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2003年 / 52卷 / 06期
关键词
D O I
10.1016/S0026-0495(03)00055-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The current study aimed to compare the effects of treatment (2 months) with thiazolidinediones (TZDs) and placebo on glucose and fat metabolism in patients with type 2 diabetes (T2DM) in a crossover design. Eight patients received placebo (2 months) followed by TZD (2 months). Two-stage (1.5 and 6.0 pmol/kg min) hyperinsulinemic-euglycemic clamps were performed in all 8 patients pre- and post-placebo and post-TZD (post-placebo = pre-TZD). We determined rates of glucose disappearance (G(Rd)), glycolysis (GLS), glycogen synthesis (GS) (all with 3-H-3 glucose), carbohydrate (CHO) oxidation (indirect calorimetry), endogenous glucose production (EGP), free fatty acid (FIFA) release (H-2(5) glycerol), and oxidation (indirect calorimetry) and re-esterification, as well as plasma adiponectin and leptin concentrations, and fat cell size and number (determined in upper thigh biopsy samples). Placebo treatment had no effects on any of the measured parameters. TZD treatment improved insulin-stimulated glucose uptake (ISGU) from 17.1 to 26.4 mumol/kg min (P < .01) and insulin-stimulated GS from 4.8 to 13.4 mumol/kg min (P < 0.03), potentiated insulin-induced suppression of lipolysis from 4.3 to 2.3 mumol/kg min (P < .03) and FFA re-esterification from 1.9 to 1.0 mumol/kg min (P < .02), increased plasma adiponectin levels from 2.7 to 7.2 mug/mL (P < .05), and decreased plasma leptin levels from 30.8 to 23.4 ng/mL (P < .02). In addition, TZD tended to increase the number of small adipocytes (<50 mum) in subcutaneous adipose tissue. We conclude that TZDs have multiple actions and that many, but perhaps not all, can be accounted for by their action on adipose tissue. (C) 2003 Elsevier Inc. All rights reserved.
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收藏
页码:753 / 759
页数:7
相关论文
共 52 条
[1]   EFFECTS OF INSULIN ON FATTY-ACID REESTERIFICATION IN HEALTHY-SUBJECTS [J].
BODEN, G ;
CHEN, XH ;
DESANTIS, RA ;
KENDRICK, Z .
DIABETES, 1993, 42 (11) :1588-1593
[2]   Role of fatty acids in the pathogenesis of insulin resistance and NIDDM [J].
Boden, G .
DIABETES, 1997, 46 (01) :3-10
[3]   Troglitazone action is independent of adipose tissue [J].
Burant, CF ;
Sreenan, S ;
Hirano, KI ;
Tai, TAC ;
Lohmiller, J ;
Lukens, J ;
Davidson, NO ;
Ross, S ;
Graves, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) :2900-2908
[4]   Fenofibrate and rosiglitazone lower serum triglycerides with opposing effects on body weight [J].
Chaput, E ;
Saladin, R ;
Silvestre, M ;
Edgar, AD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 271 (02) :445-450
[5]   Impaired glucose transport as a cause of decreased insulin-stimulated muscle glycogen synthesis in type 2 diabetes [J].
Cline, GW ;
Petersen, KF ;
Krssak, M ;
Shen, J ;
Hundal, RS ;
Trajanoski, Z ;
Inzucchi, S ;
Dresner, A ;
Rothman, DL ;
Shulman, GI .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (04) :240-246
[6]   Modulation of insulin activities by leptin [J].
Cohen, B ;
Novick, D ;
Rubinstein, M .
SCIENCE, 1996, 274 (5290) :1185-1188
[7]   Endogenous glucose production is inhibited by the adipose-derived protein Acrp30 [J].
Combs, TP ;
Berg, AH ;
Obici, S ;
Scherer, PE ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (12) :1875-1881
[8]   Effects of pioglitazone on adipose tissue remodeling within the setting of obesity and insulin resistance [J].
de Souza, CJ ;
Eckhardt, M ;
Gagen, K ;
Dong, M ;
Chen, W ;
Laurent, D ;
Burkey, BF .
DIABETES, 2001, 50 (08) :1863-1871
[9]   THE EFFECT OF INSULIN ON THE DISPOSAL OF INTRAVENOUS GLUCOSE - RESULTS FROM INDIRECT CALORIMETRY AND HEPATIC AND FEMORAL VENOUS CATHETERIZATION [J].
DEFRONZO, RA ;
JACOT, E ;
JEQUIER, E ;
MAEDER, E ;
WAHREN, J ;
FELBER, JP .
DIABETES, 1981, 30 (12) :1000-1007
[10]   REGULATION OF GLUCOSE-TRANSPORT BY PIOGLITAZONE IN CULTURED MUSCLE-CELLS [J].
ELKEBBI, IM ;
ROSER, S ;
POLLET, RJ .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1994, 43 (08) :953-958