Increased fatty acid uptake and altered fatty acid metabolism in insulin-resistant muscle of obese Zucker rats

被引:77
作者
Turcotte, LP
Swenberger, JR
Tucker, MZ
Yee, AJ
机构
[1] Univ So Calif, Dept Kinesiol, Los Angeles, CA 90089 USA
[2] Univ So Calif, Ctr Diabet, Los Angeles, CA 90089 USA
关键词
D O I
10.2337/diabetes.50.6.1389
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Altered muscle fatty acid (FA) metabolism may contribute to the presence of muscle insulin resistance in the genetically obese Zucker rat. To determine whether FA uptake and disposal are altered in insulin-resistant muscle, we measured palmitate uptake, oxidation, and incorporation into di- and triglycerides in isolated rat hindquarters, as well as muscle plasma membrane fatty acid-binding protein (FABP(PM)) content of lean (n = 16, f alpha/+) and obese (n = 15,f alpha /f alpha) Zucker rats (12 weeks of age). Hindquarters were perfused with 7 mmol/l glucose, 1,000 mu mol/l albumin-bound palmitate, and albumin-bound [1-C-14]palmitate at rest (no insulin). Glucose uptake was 42% lower in the obese than in the lean rats and indicated the presence of muscle insulin resistance. Fractional and total rates of palmitate uptake were 42 and 74% higher in the obese than in the lean rats and were associated with higher muscle FAB(PM), content (r(2) = 0.69, P < 0.05). The percentage of palmitate oxidized was not significantly different between groups. FA disposal to storage was altered according to fiber type. When compared with lean rats, the rate of triglyceride synthesis in red muscle was 158% higher in obese rats, and the rate of palmitate incorporation into diglycerides in white muscle was 93% higher in obese rats. Pre- and postperfusion muscle triglyceride levels mere higher in both red and white muscles of the obese rats. These results show that increased FA uptake and altered FA disposal to storage may contribute to the development of muscle insulin resistance in obese Zucker rats.
引用
收藏
页码:1389 / 1396
页数:8
相关论文
共 47 条
[11]   DECREASED EXPRESSION OF PROTEIN-KINASE-C ALPHA,BETA, AND EPSILON IN SOLEUS MUSCLE OF ZUCKER OBESE (FA/FA) RATS [J].
COOPER, DR ;
WATSON, JE ;
DAO, ML .
ENDOCRINOLOGY, 1993, 133 (05) :2241-2247
[12]   INSULIN RESISTANCE IN SOLEUS MUSCLE FROM OBESE ZUCKER RATS - INVOLVEMENT OF SEVERAL DEFECTIVE SITES [J].
CRETTAZ, M ;
PRENTKI, M ;
ZANINETTI, D ;
JEANRENAUD, B .
BIOCHEMICAL JOURNAL, 1980, 186 (02) :525-534
[13]   ELEVATED MUSCLE CITRATE DOES NOT REDUCE CARBOHYDRATE UTILIZATION DURING TETANIC STIMULATION [J].
DYCK, DJ ;
SPRIET, LL .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1994, 72 (02) :117-125
[14]   Functional differences in lipid metabolism in resting skeletal muscle of various fiber types [J].
Dyck, DJ ;
Peters, SJ ;
Glatz, J ;
Gorski, J ;
Keizer, H ;
Kiens, B ;
Liu, S ;
Righter, EA ;
Spriet, LL ;
VanderVusse, GJ ;
Bonen, A .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (03) :E340-E351
[15]   Effect of extracellular palmitate on 2-deoxy-D-glucose uptake in muscle from ad libitum fed and calorie restricted rats [J].
Gazdag, AC ;
Tucker, MZ ;
Turcotte, LP ;
Dean, DJ ;
Cartee, GD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 252 (03) :733-737
[16]   BLOOD-FLOW DISTRIBUTION IN TISSUES OF PERFUSED RAT HINDLIMB PREPARATIONS [J].
GORSKI, J ;
HOOD, DA ;
TERJUNG, RL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 250 (04) :E441-E448
[17]   SYNTHESIS AND SECRETION OF VERY LOW-DENSITY LIPOPROTEINS BY ISOLATED RAT HEPATOCYTES IN SUSPENSION - ROLE OF DIACYLGLYCEROL ACYLTRANSFERASE [J].
HAAGSMAN, HP ;
VANGOLDE, LMG .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1981, 208 (02) :395-402
[18]   EFFECT OF GLUCOSE AND INSULIN ON TRIACYLGLYCEROL METABOLISM IN ISOLATED NORMAL AND DIABETIC SKELETAL-MUSCLE [J].
HOPP, JF ;
PALMER, WK .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1991, 40 (03) :223-225
[19]   ELECTRICAL-STIMULATION ALTERS FATTY-ACID METABOLISM IN ISOLATED SKELETAL-MUSCLE [J].
HOPP, JF ;
PALMER, WK .
JOURNAL OF APPLIED PHYSIOLOGY, 1990, 68 (06) :2473-2481
[20]   Muscle-specific overexpression of FAT/CD36 enhances fatty acid oxidation by contracting muscle, reduces plasma triglycerides and fatty acids, and increases plasma glucose and insulin [J].
Ibrahimi, A ;
Bonen, A ;
Blinn, WD ;
Hajri, T ;
Li, X ;
Zhong, K ;
Cameron, R ;
Abumrad, NA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) :26761-26766