Muscle GLUT4 in cirrhosis

被引:3
|
作者
Holland-Fischer, Peter [1 ]
Andersen, Per Heden
Lund, Sten
Pedersen, Steen Bonnelykke
Vinter-Jensen, Lars
Nielsen, Michael F.
Kaal, Andreas
Dall, Rolf
Schmitz, Ole
Vilstrup, Hendrik
机构
[1] Aarhus Univ Hosp, Depv Med Hepatol & Gastroenterol 5, 44 Noerrebrogade, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Med Endocrinol M, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ Hosp, Dept Med Endocrinol C, DK-8000 Aarhus C, Denmark
[4] Aarhus Univ Hosp, Dept Anesthesiol, DK-8000 Aarhus C, Denmark
关键词
GLUT4; liver cirrhosis; skeletal muscle; glucose intolerance; insulin resistance; clinical research;
D O I
10.1016/j.jhep.2007.02.012
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The insulin-dependent glucose transporter GLUT4 mediates 50-80% of whole body glucose uptake, but its relation to the frequent glucose intolerance in patients with liver cirrhosis is unknown. Methods:Thirty patients and seven healthy controls underwent a 2-h oral glucose tolerance test and later a muscle biopsy. Levels of GLUT4 total protein and mRNA content were determined in muscle biopsies by polyclonal antibody labelling and RT-PCR, respectively. Results: GLUT4 protein content in the cirrhosis group was not different from that of the controls, but at variance with the control subjects it correlated closely with measures of glucose tolerance (R-2 = 0.45; p = 0.003). GLUT4 mRNA of the patients with cirrhosis was reduced to 56% of control value (95%0 ci: 27-86%; p = 0.015) and was inversely related to the level of basal hyper-insulinemia (R-2 = 0.39; p = 0.004). Conclusions: In cirrhosis GLUT4 protein content was quantitatively intact, while limiting glucose tolerance. This indicates loss of redundancy of the major glucose transport system, possibly related to the markedly decreased expression of its gene. Hyper-insulinemia may be a primary event. Our findings implicate the muscular GLUT4 system in the glucose intolerance of liver cirrhosis by a mechanism different from that in diabetes. (C) 2007 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:212 / 219
页数:8
相关论文
共 50 条
  • [21] The GLUT4 code
    Larance, Mark
    Ramm, Georg
    James, David E.
    MOLECULAR ENDOCRINOLOGY, 2008, 22 (02) : 226 - 233
  • [22] Reexpression of GLUT4 in GLUT4 null hearts abolishes cardiac hypertrophy
    Laidlaw, JS
    Tsao, TS
    Jelicks, LA
    Factor, S
    Charron, MJ
    DIABETES, 2000, 49 : A285 - A286
  • [23] REGULATION BY EXERCISE OF SKELETAL MUSCLE CONTENT OF MITOCHONDRIA AND GLUT4
    Holloszy, J. O.
    JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2008, 59 (04): : 5 - 18
  • [24] Vanadium increases GLUT4 in diabetic rat skeletal muscle
    Askar Mohammad
    Vijay Sharma
    John H. McNeill
    Molecular and Cellular Biochemistry, 2002, 233 : 139 - 143
  • [25] Peptide rescues GLUT4 recruitment, but not GLUT4 activation, in insulin resistance
    Funaki, Makoto
    Benincasa, Kate
    Randhawa, Paramjeet K.
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 360 (04) : 891 - 896
  • [26] Epigallocatechin gallate promotes GLUT4 translocation in skeletal muscle
    Ueda, Manabu
    Nishiumi, Shin
    Nagayasu, Hironobu
    Fukuda, Itsuko
    Yoshida, Ken-ichi
    Ashida, Hitoshi
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 377 (01) : 286 - 290
  • [27] Trafficking pathway of GLUT4 glucose transporters in muscle (Review)
    Zorzano, A
    Sevilla, L
    Tomas, E
    Camps, M
    Guma, A
    Palacin, M
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 1998, 2 (03) : 263 - 271
  • [28] The role of CaMKII in regulating GLUT4 expression in skeletal muscle
    Ojuka, Edward O.
    Goyaram, Veeraj
    Smith, James A. H.
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2012, 303 (03): : E322 - E331
  • [29] Push/pull mechanisms of GLUT4 traffic in muscle cells
    Rudich, A
    Klip, A
    ACTA PHYSIOLOGICA SCANDINAVICA, 2003, 178 (04): : 297 - 308
  • [30] Vanadium increases GLUT4 in diabetic rat skeletal muscle
    Mohammad, A
    Sharma, V
    McNeill, JH
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 233 (1-2) : 139 - 143