EFFECTS OF EXERCISE TRAINING AND DIETARY MANIPULATION ON INSULIN-REGULATABLE GLUCOSE-TRANSPORTER MESSENGER-RNA IN RAT MUSCLE

被引:54
作者
WAKE, SA
SOWDEN, JA
STORLIEN, LH
JAMES, DE
CLARK, PW
SHINE, J
CHISHOLM, DJ
KRAEGEN, EW
机构
[1] ST VINCENTS HOSP,GARVAN INST MED RES,DARLINGHURST,NSW 2010,AUSTRALIA
[2] WASHINGTON UNIV,SCH MED,DEPT CELL BIOL & PHYSIOL,ST LOUIS,MO 63110
关键词
D O I
10.2337/diabetes.40.2.275
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Both exercise training and dietary manipulation (increasing omega-3/omega-6 fat ratio) can ameliorate insulin resistance caused by a high-fat diet in rats. We determined whether alterations in the expression of the insulin-regulatable (IR) and/or HepG2 glucose-transporter (GT) mRNAs were similarly affected. There was a significantly higher level of IRGT mRNA in skeletal muscle from exercise-trained versus sedentary high-fat-fed rats (27% increase, P < 0.01). This difference is consistent with previously reported increases in muscle insulin-mediated glucose uptake. Skeletal muscle HepG2GT mRNA was too low to detect any training effect, but there was a tendency toward higher levels with training in cardiac muscle. In contrast, dietary manipulation, previously shown to lead to a much greater increase (100-300%) in muscle insulin-mediated glucose uptake, did not change IRGT or HepG2GT mRNA in skeletal muscle or heart. Thus, both dietary manipulation and exercise training increase insulin-stimulated glucose uptake in skeletal muscle, but only exercise training increases IRGT mRNA. Therefore, exercise training apparently increases GT production, whereas dietary manipulation improves glucose transport in skeletal muscle by other mechanisms.
引用
收藏
页码:275 / 279
页数:5
相关论文
共 27 条
[1]   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
[2]   IDENTIFICATION OF A NOVEL GENE ENCODING AN INSULIN-RESPONSIVE GLUCOSE TRANSPORTER PROTEIN [J].
BIRNBAUM, MJ .
CELL, 1989, 57 (02) :305-315
[3]   CLONING AND CHARACTERIZATION OF A CDNA-ENCODING THE RAT-BRAIN GLUCOSE-TRANSPORTER PROTEIN [J].
BIRNBAUM, MJ ;
HASPEL, HC ;
ROSEN, OM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :5784-5788
[4]   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
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   SEQUENCE, TISSUE DISTRIBUTION, AND CHROMOSOMAL LOCALIZATION OF MESSENGER-RNA ENCODING A HUMAN GLUCOSE TRANSPORTER-LIKE PROTEIN [J].
FUKUMOTO, H ;
SEINO, S ;
IMURA, H ;
SEINO, Y ;
EDDY, RL ;
FUKUSHIMA, Y ;
BYERS, MG ;
SHOWS, TB ;
BELL, GI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (15) :5434-5438
[7]   PRETRANSLATIONAL SUPPRESSION OF AN INSULIN-RESPONSIVE GLUCOSE TRANSPORTER IN RATS WITH DIABETES-MELLITUS [J].
GARVEY, WT ;
HUECKSTEADT, TP ;
BIRNBAUM, MJ .
SCIENCE, 1989, 245 (4913) :60-63
[8]   ISOLATION AND CHARACTERIZATION OF FULL-LENGTH CDNA CLONES FOR HUMAN ALPHA-ACTIN, BETA-ACTIN AND GAMMA-ACTIN MESSENGER-RNAS - SKELETAL BUT NOT CYTOPLASMIC ACTINS HAVE AN AMINO-TERMINAL CYSTEINE THAT IS SUBSEQUENTLY REMOVED [J].
GUNNING, P ;
PONTE, P ;
OKAYAMA, H ;
ENGEL, J ;
BLAU, H ;
KEDES, L .
MOLECULAR AND CELLULAR BIOLOGY, 1983, 3 (05) :787-795
[9]   A POSSIBLE MECHANISM OF INSULIN RESISTANCE IN THE RAT ADIPOSE CELL WITH HIGH-FAT LOW-CARBOHYDRATE FEEDING - DEPLETION OF INTRACELLULAR GLUCOSE-TRANSPORT SYSTEMS [J].
HISSIN, PJ ;
KARNIELI, E ;
SIMPSON, IA ;
SALANS, LB ;
CUSHMAN, SW .
DIABETES, 1982, 31 (07) :589-592
[10]   EFFECT OF EXERCISE TRAINING ON WHOLE-BODY INSULIN SENSITIVITY AND RESPONSIVENESS [J].
JAMES, DE ;
KRAEGEN, EW ;
CHISHOLM, DJ .
JOURNAL OF APPLIED PHYSIOLOGY, 1984, 56 (05) :1217-1222