INCREASED BASAL GLUCOSE-PRODUCTION IN TYPE-1 GAUCHERS-DISEASE

被引:28
作者
CORSSMIT, EPM
HOLLAK, CEM
ENDERT, E
VANOERS, MHJ
SAUERWEIN, HP
ROMIJN, JA
机构
[1] UNIV AMSTERDAM, ACAD MED CTR, DEPT ENDOCRINOL, 1105 AZ AMSTERDAM, NETHERLANDS
[2] UNIV AMSTERDAM, ACAD MED CTR, DEPT CRIT CARE, 1105 AZ AMSTERDAM, NETHERLANDS
关键词
D O I
10.1210/jc.80.9.2653
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate the metabolic effects of Gaucher's disease, glucose metabolism and parameters of fat metabolism were studied by indirect calorimetry and primed continuous infusion of [3-H-3]glucose in seven clinically stable untreated patients with type 1 Gaucher's disease and in seven healthy matched control subjects. Studies were performed in the postabsorptive state. In Gaucher patients, resting energy expenditure was increased by similar to 24% (29.4 +/- 0.7 vs. 23.7 +/- 0.8 kcal/kg . day; P < 0.01). Glucose production was increased by similar to 30% in patients compared to controls (14.00 +/- 0.51 vs. 10.77 +/- 0.26; P < 0.01), although plasma glucose concentrations and net glucose oxidation were not different, Although C peptide concentrations were not different, insulin concentrations were slightly increased in Gaucher patients (P < 0.05). The differences in basal glucose production were not related to differences in plasma concentrations of insulin or other glucoregulatory hormones. In conclusion, the increase in basal glucose production is a remarkable feature of type 1 Gaucher's disease, which cannot merely be explained by endocrine mechanisms. Because Gaucher's disease is manifested within the liver in macrophages, but not in hepatocytes, altered intrahepatic regulatory mechanisms might be involved in this increase in glucose production.
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收藏
页码:2653 / 2657
页数:5
相关论文
共 27 条
[1]   DEFICIENT ACTIVITY OF GLUCOCEREBROSIDASE IN URINE FROM PATIENTS WITH TYPE-1 GAUCHER DISEASE [J].
AERTS, JMFG ;
DONKERKOOPMAN, WE ;
KOOT, M ;
BARRANGER, JA ;
TAGER, JM ;
SCHRAM, AW .
CLINICA CHIMICA ACTA, 1986, 158 (02) :155-163
[2]  
Barranger J. A., 1989, METABOLIC BASIS INHE, P1677
[3]   RESTING ENERGY-EXPENDITURE IN GAUCHERS-DISEASE TYPE-1 - EFFECT OF GAUCHERS CELL BURDEN ON ENERGY-REQUIREMENTS [J].
BARTON, DJ ;
LUDMAN, MD ;
BENKOV, K ;
GRABOWSKI, GA ;
LELEIKO, NS .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1989, 38 (12) :1238-1243
[4]  
CASTELEIJN E, 1988, J BIOL CHEM, V263, P2699
[5]   INDOMETHACIN STIMULATES BASAL GLUCOSE-PRODUCTION IN HUMANS WITHOUT CHANGES IN CONCENTRATIONS OF GLUCOREGULATORY HORMONES [J].
CORSSMIT, EPM ;
ROMIJN, JA ;
ENDERT, E ;
SAUERWEIN, HP .
CLINICAL SCIENCE, 1993, 85 (06) :679-685
[6]   PENTOXIFYLLINE INHIBITS BASAL GLUCOSE-PRODUCTION IN HUMANS [J].
CORSSMIT, EPM ;
ROMIJN, JA ;
ENDERT, E ;
SAUERWEIN, HP .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (06) :2767-2772
[7]  
DANIELS LB, 1982, CLIN CHEM, V28, P569
[8]   EICOSANOIDS, SIGNAL MOLECULES OF LIVER-CELLS [J].
DECKER, K .
SEMINARS IN LIVER DISEASE, 1985, 5 (02) :175-190
[9]   BIOLOGICALLY-ACTIVE PRODUCTS OF STIMULATED LIVER MACROPHAGES (KUPFFER CELLS) [J].
DECKER, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 192 (02) :245-261
[10]   FASTING HYPERGLYCEMIA IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS - CONTRIBUTIONS OF EXCESSIVE HEPATIC GLUCOSE-PRODUCTION AND IMPAIRED TISSUE GLUCOSE-UPTAKE [J].
DEFRONZO, RA ;
FERRANNINI, E ;
SIMONSON, DC .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1989, 38 (04) :387-395