INTERACTION OF INSULIN AND EXERCISE ON GLUCOSE-TRANSPORT IN MUSCLE

被引:43
作者
RODNICK, KJ
PIPER, RC
SLOT, JW
JAMES, DE
机构
[1] WASHINGTON UNIV, SCH MED,DEPT CELL BIOL & PHYSIOL,BOX 8228, 660 S EUCLID AVE, ST LOUIS, MO 63110 USA
[2] WASHINGTON UNIV, SCH MED, DEPT MED, ST LOUIS, MO 63110 USA
[3] UNIV UTRECHT, SCH MED, DEPT CELL BIOL, UTRECHT, NETHERLANDS
关键词
D O I
10.2337/diacare.15.11.1679
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucose transport is the rate-limiting step for glucose utilization in muscle. In muscle and adipose tissue, glucose transport is acutely regulated by such factors as insulin and exercise. Translocation of glucose transporters (GLUT4) from an intracellular domain to the cell surface is the major mechanism for this regulation. Using immunocytochemistry, the intracellular distribution of GLUT4 under resting conditions is similar in adipocytes and myocytes. GLUT4 is concentrated in tubulovesicular structures either in the trans-Golgi region or in the cytosol, often close to the cell surface but not on the cell surface. After stimulation, cell surface GLUT4 labeling is increased by as much as 40-fold. GLUT4 is chronically regulated by altered gene expression. Neural and/or contractile activity regulates GLUT4 expression in muscle: 1) GLUT4 levels differ among muscles of different fiber type; 2) GLUT4 levels in muscle are increased with exercise training and decreased with denervation; and 3) cultured muscle cells, which lack an intact nerve supply, express very low levels of GLUT4. GLUT4 expression appears to be regulated in parallel with many oxidative enzymes in muscle, suggesting that there may be a unified developmental program that determines the overall metabolic properties of a particular muscle. Preliminary evidence suggests that impaired GLUT4 expression in muscle is not the primary defect associated with insulin resistance. Nevertheless, it is conceivable that the adaptive increase in muscle GLUT4 that is nd with exercise training may have beneficial effects in insulin-resistant states such non-insulin-dependent diabetes.
引用
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页码:1679 / 1689
页数:11
相关论文
共 89 条
[1]  
ARMSTRONG RB, 1984, AM J ANAT, V171, P259, DOI 10.1002/aja.1001710303
[2]   MOLECULAR-BIOLOGY OF MAMMALIAN GLUCOSE TRANSPORTERS [J].
BELL, GI ;
KAYANO, T ;
BUSE, JB ;
BURANT, CF ;
TAKEDA, J ;
LIN, D ;
FUKUMOTO, H ;
SEINO, S .
DIABETES CARE, 1990, 13 (03) :198-208
[3]   DECREASED EXPRESSION OF THE INSULIN-RESPONSIVE GLUCOSE TRANSPORTER IN DIABETES AND FASTING [J].
BERGER, J ;
BISWAS, C ;
VICARIO, PP ;
STROUT, HV ;
SAPERSTEIN, R ;
PILCH, PF .
NATURE, 1989, 340 (6228) :70-72
[4]   IDENTIFICATION OF A NOVEL GENE ENCODING AN INSULIN-RESPONSIVE GLUCOSE TRANSPORTER PROTEIN [J].
BIRNBAUM, MJ .
CELL, 1989, 57 (02) :305-315
[5]   INSULIN-INDUCED TRANSLOCATION OF GLUCOSE TRANSPORTERS FROM POST-GOLGI COMPARTMENTS TO THE PLASMA-MEMBRANE OF 3T3-L1 ADIPOCYTES [J].
BLOK, J ;
GIBBS, EM ;
LIENHARD, GE ;
SLOT, JW ;
GEUZE, HJ .
JOURNAL OF CELL BIOLOGY, 1988, 106 (01) :69-76
[6]   INSULIN BINDING AND GLUCOSE-UPTAKE DIFFERENCES IN RODENT SKELETAL-MUSCLES [J].
BONEN, A ;
TAN, MH ;
WATSONWRIGHT, WM .
DIABETES, 1981, 30 (08) :702-704
[7]   TRANSLOCATION OF THE BRAIN-TYPE GLUCOSE TRANSPORTER LARGELY ACCOUNTS FOR INSULIN STIMULATION OF GLUCOSE-TRANSPORT IN BC3H-1 MYOCYTES [J].
CALDERHEAD, DM ;
KITAGAWA, K ;
LIENHARD, GE ;
GOULD, GW .
BIOCHEMICAL JOURNAL, 1990, 269 (03) :597-601
[8]   A GLUCOSE-TRANSPORT PROTEIN EXPRESSED PREDOMINATELY IN INSULIN-RESPONSIVE TISSUES [J].
CHARRON, MJ ;
BROSIUS, FC ;
ALPER, SL ;
LODISH, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (08) :2535-2539
[9]  
CHARRON MJ, 1990, J BIOL CHEM, V265, P7994
[10]   BIOCHEMICAL AND FUNCTIONAL-CHARACTERIZATION OF THE RAT-LIVER GLUCOSE-TRANSPORT SYSTEM - COMPARISONS WITH THE ADIPOCYTE GLUCOSE-TRANSPORT SYSTEM [J].
CIARALDI, TP ;
HORUK, R ;
MATTHAEI, S .
BIOCHEMICAL JOURNAL, 1986, 240 (01) :115-123