Interleukin-6 secretion in mice is associated with reduced glucose-6-phosphatase and liver glycogen levels

被引:35
作者
Metzger, S
Goldschmidt, N
Barash, V
Peretz, T
Drize, O
Shilyansky, J
Shiloni, E
ChajekShaul, T
机构
[1] HADASSAH UNIV HOSP, DIV MED, IL-91120 JERUSALEM, ISRAEL
[2] HADASSAH UNIV HOSP, DIV CLIN BIOCHEM, IL-91120 JERUSALEM, ISRAEL
[3] HADASSAH UNIV HOSP, DIV ONCOL, IL-91120 JERUSALEM, ISRAEL
[4] HADASSAH UNIV HOSP, DIV SURG, IL-91120 JERUSALEM, ISRAEL
[5] UNIV TORONTO, HOSP SICK CHILDREN, DEPT SURG, TORONTO, ON M5G 1H4, CANADA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1997年 / 273卷 / 02期
关键词
phosphoenolpyruvate carboxykinase; gene expression;
D O I
10.1152/ajpendo.1997.273.2.E262
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mice bearing interleukin-6 (IL-6)-secreting tumor were used to study the chronic effect of IL-6 on carbohydrate metabolism. Mice were injected with allogeneic tumor cells transduced with the murine IL-6 gene. Serum IL-6 levels were correlated exponentially with tumor weight. Secretion of IL-6 from the developed tumors was associated with decreased food consumption, reduced body weight, and reduced blood glucose levels. Insulin levels did not change, and 2-deoxyglucose uptake was not affected in most tissues examined. A significant increase of 2-deoxyglucose uptake was measured in the liver. Glycogen content in the liver determined 0, 6, 12, and 18 days after tumor inoculation was 42, 23, 12, and 3 mg/g, respectively. The activity of phosphoenolpyruvate carboxykinase was not affected. The activity of glucose-6-phosphatase (G-6-Pase) determined 6, 12, and 18 days after tumor injection was 84, 70, and 50% of G-6-Pase activity in pair-fed mice bearing nonsecreting tumors, respectively. G-6-Pase mRNA levels were markedly reduced due to inhibition of G-6-Pase gene transcriptional rate.
引用
收藏
页码:E262 / E267
页数:6
相关论文
共 30 条
  • [1] MOLECULAR-CLONING OF APRF, A NOVEL IFN-STIMULATED GENE FACTOR-3 P91-RELATED TRANSCRIPTION FACTOR INVOLVED IN THE GP130-MEDIATED SIGNALING PATHWAY
    AKIRA, S
    NISHIO, Y
    INOUE, M
    WANG, XJ
    WEI, S
    MATSUSAKA, T
    YOSHIDA, K
    SUDO, T
    NARUTO, M
    KISHIMOTO, T
    [J]. CELL, 1994, 77 (01) : 63 - 71
  • [2] AMSSILLON D, 1996, J BIOL CHEM, V271, P9871
  • [3] ARION WJ, 1980, J BIOL CHEM, V255, P396
  • [4] DYSREGULATED INTERLEUKIN-6 EXPRESSION PRODUCES A SYNDROME RESEMBLING CASTLEMANS DISEASE IN MICE
    BRANDT, SJ
    BODINE, DM
    DUNBAR, CE
    NIENHUIS, AW
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (02) : 592 - 599
  • [5] A NEW MICROTECHNIQUE FOR THE ANALYSIS OF THE HUMAN HEPATIC-MICROSOMAL GLUCOSE-6-PHOSPHATASE SYSTEM
    BURCHELL, A
    HUME, R
    BURCHELL, B
    [J]. CLINICA CHIMICA ACTA, 1988, 173 (02) : 183 - 192
  • [6] LETHAL HYPOGLYCEMIA AND HYPOTHERMIA INDUCED BY ADMINISTRATION OF LOW-DOSES OF TUMOR-NECROSIS-FACTOR TO ADRENALECTOMIZED RATS
    CHAJEKSHAUL, T
    BARASH, V
    WEIDENFELD, J
    FRIEDMAN, G
    ZIV, E
    SHOHAMI, E
    SHILONI, E
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1990, 39 (03): : 242 - 250
  • [7] CHANG HC, 1966, J BIOL CHEM, V241, P2413
  • [8] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [9] COMBATES NJ, 1994, J BIOL CHEM, V269, P29719
  • [10] DEFECTIVE INFLAMMATORY RESPONSE IN INTERLEUKIN 6-DEFICIENT MICE
    FATTORI, E
    CAPPELLETTI, M
    COSTA, P
    SELLITTO, C
    CANTONI, L
    CARELLI, M
    FAGGIONI, R
    FANTUZZI, G
    GHEZZI, P
    POLI, V
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) : 1243 - 1250