EFFECTS OF ALTERED GLUCOSE-HOMEOSTASIS ON GLUCOSE TRANSPORTER EXPRESSION IN SKELETAL-MUSCLE OF THE RAT

被引:96
作者
BOUREY, RE
KORANYI, L
JAMES, DE
MUECKLER, M
PERMUTT, MA
机构
[1] WASHINGTON UNIV,SCH MED,DEPT MED,660 S EUCLID AVE,BOX 8127,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,DEPT CELL BIOL,ST LOUIS,MO 63110
关键词
Diabetes; Fasting; GLUT-4; gene; Hypoglycemia; Rat soleus;
D O I
10.1172/JCI114742
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Previous studies have suggested that alteration in the expression of the insulin-regulatable glucose transporter of muscle (GLUT-4 protein) may be an important determinant of insulin action. In the present studies, we have examined GLUT-4 mRNA and protein concentrations in muscle after variations in the metabolic status of the intact animal (i.e., 7 d streptozotocin-induced diabetes, 7 d insulin-induced hypoglycemia, and 3 d fasting). These changes in glucose homeostasis were associated with the following changes in GLUT-4 gene products: a decrease of ∼ 30% in both mRNA and protein with diabetes; a 50% increase in mRNA and a 2.4-fold increase in protein with insulin injection; and normal mRNA in spite of a 2.7-fold increase in protein with fasting. Fasted diabetics exhibited an increase of 50% in GLUT-4 mRNA and a 2.4-fold increase in protein relative to fed diabetics. In diabetic and insulin-injected groups, the changes in GLUT-4 protein were similar to changes in mRNA, but in fasting, GLUT-4 protein increased without a concomitant change in mRNA. Overall there was no correlation between muscle concentrations of GLUT-4 protein and mRNA. Muscle GLUT-4 protein concentration tended to correlate with plasma glucose (r = -0.57, P < 0.001), but not with plasma insulin. These results indicate that (a) chronic changes in glucose homeostasis are associated with changes in expression of GLUT-4 protein in muscle; (b) GLUT-4 protein increased in fasted soleus muscle without change in mRNA, thereby differing from fasted adipocytes in which both GLUT-4 products diminish; and (c) no simple relationship exists between total muscle GLUT-4 protein content and whole-body insulin sensitivity.
引用
收藏
页码:542 / 547
页数:6
相关论文
共 30 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]   INSULIN BINDING AND SENSITIVITY IN RAT SKELETAL-MUSCLE - EFFECT OF STARVATION [J].
BRADY, LJ ;
GOODMAN, MN ;
KALISH, FN ;
RUDERMAN, NB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1981, 240 (02) :E184-E190
[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]   EFFECTS OF INSULIN ON PERIPHERAL AND SPLANCHNIC GLUCOSE-METABOLISM IN NONINSULIN-DEPENDENT (TYPE-II) DIABETES-MELLITUS [J].
DEFRONZO, RA ;
GUNNARSSON, R ;
BJORKMAN, O ;
OLSSON, M ;
WAHREN, J .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (01) :149-155
[7]   AN INVITRO HUMAN MUSCLE PREPARATION SUITABLE FOR METABOLIC STUDIES - DECREASED INSULIN STIMULATION OF GLUCOSE-TRANSPORT IN MUSCLE FROM MORBIDLY OBESE AND DIABETIC SUBJECTS [J].
DOHM, GL ;
TAPSCOTT, EB ;
PORIES, WJ ;
DABBS, DJ ;
FLICKINGER, EG ;
MEELHEIM, D ;
FUSHIKI, T ;
ATKINSON, SM ;
ELTON, CW ;
CARO, JF .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (02) :486-494
[8]  
FUKUMOTO H, 1989, J BIOL CHEM, V264, P776
[9]   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
[10]   EFFECTS OF FASTING ON TISSUE GLUCOSE-UTILIZATION IN CONSCIOUS RESTING RATS - MAJOR GLUCOSE-SPARING EFFECT IN WORKING MUSCLES [J].
ISSAD, T ;
PENICAUD, L ;
FERRE, P ;
KANDE, J ;
BAUDON, MA ;
GIRARD, J .
BIOCHEMICAL JOURNAL, 1987, 246 (01) :241-244