Sucrose diets increase glucose-6-phosphatase and glucose release and decrease glucokinase in hepatocytes

被引:4
作者
Bizeau, ME
Thresher, JS
Pagliassotti, MJ
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Med, Div Endocrinol Diabet & Metab, Denver, CO 80262 USA
[2] Arizona State Univ, Exercise & Sport Res Inst, Tempe, AZ 85287 USA
关键词
liver; diet composition; glucose production;
D O I
10.1152/jappl.2001.91.5.2041
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
A high-sucrose diet (SU) decreases insulin action in the liver (Pagliassotti MJ, Shahrokhi KA, and Moscarello M. Am J Physiol Regulatory Integrative Comp Physiol 266: R1637-R1644, 1994). The present study was conducted to characterize the effect of SU on glucagon action in isolated periportal (PP) and perivenous (PV) hepatocytes by measuring glucagon-stimulated glycogenolysis and glucose release. Male rats were fed a SU (68% sucrose) or starch diet (ST, 68% starch) for 1 wk, and hepatocytes were isolated from PP or PV regions (n = 4/diet/cell population). Hepatocytes were incubated for 1 h in the presence of varying concentrations of glucagon (0-100 nM). In PP and PV cells, glucagon stimulation of glucose release and glycogenolysis (sum of glucose release and lactate accumulation) was not significantly different between SU and ST cells. However, in the SU PP cells, glucose release was increased compared with ST PP cells, both in the absence of glucagon (76.1 +/- 4 vs. 54.8 +/- 3 nmol.h(-1).mg cell wet wt(-1)) and at all glucagon concentrations. In SU-fed PV cells, glucose release was increased compared with ST PV cells in the absence of glucagon (79.3 +/- 5 vs. 56.4 +/- 5 nmol.h(-1) . mg cell wet wt(-1)) and at low glucagon concentrations. Maximal glucose-6-phosphatase activity (in nmol.min(-1).mg protein(-1)) was elevated in SU compared with ST cells (61.4 +/- 3 vs. 37.5 +/- 4 in PP and 37.5 +/- 4 vs. 29.5 +/- 3 in PV cells). In contrast, maximal glucokinase activity (in nmol . min(-1) . mg protein(-1)) was elevated in ST compared with SU cells (15.9 +/- 2 vs. 12.1 +/- 1 in PP and 19.4 +/- 2 vs. 14.2 +/- 1 in PV cells). These data demonstrate that SU increases the capacity for glucose release in both PP and PV hepatocytes, in part because of reciprocal changes in glucose-6-phosphatase and glucokinase.
引用
收藏
页码:2041 / 2046
页数:6
相关论文
共 24 条
[1]   The physiological role of glucokinase binding and translocation in hepatocytes [J].
Agius, L .
ADVANCES IN ENZYME REGULATION, VOL 38, 1998, 38 :303-331
[2]   HIGH-YIELD PREPARATION OF ISOLATED RAT LIVER PARENCHYMAL CELLS - A BIOCHEMICAL AND FINE STRUCTURAL STUDY [J].
BERRY, MN ;
FRIEND, DS .
JOURNAL OF CELL BIOLOGY, 1969, 43 (03) :506-+
[3]   Dietary fat type alters glucose metabolism in isolated rat hepatocytes [J].
Bizeau, ME ;
Hazel, JR .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1999, 10 (12) :709-715
[4]   A high-sucrose diet increases gluconeogenic capacity in isolated periportal and perivenous rat hepatocytes [J].
Bizeau, ME ;
Thresher, JS ;
Pagliassotti, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 280 (05) :E695-E702
[5]   A NEW MICROTECHNIQUE FOR THE ANALYSIS OF THE HUMAN HEPATIC-MICROSOMAL GLUCOSE-6-PHOSPHATASE SYSTEM [J].
BURCHELL, A ;
HUME, R ;
BURCHELL, B .
CLINICA CHIMICA ACTA, 1988, 173 (02) :183-192
[6]   RAPID METHOD FOR DETERMINATION OF GLYCOGEN CONTENT AND RADIOACTIVITY IN SMALL QUANTITIES OF TISSUE OR ISOLATED HEPATOCYTES [J].
CHAN, TM ;
EXTON, JH .
ANALYTICAL BIOCHEMISTRY, 1976, 71 (01) :96-105
[7]   ZONATION OF GLYCOGEN AND GLUCOSE SYNTHESES, BUT NOT GLYCOLYSIS, IN RAT-LIVER [J].
CHEN, KS ;
KATZ, J .
BIOCHEMICAL JOURNAL, 1988, 255 (01) :99-104
[8]   FACTORS UNDERLYING SIGNIFICANT UNDERESTIMATIONS OF GLUCOKINASE ACTIVITY IN CRUDE LIVER EXTRACTS - PHYSIOLOGICAL IMPLICATIONS OF HIGHER CELLULAR-ACTIVITY [J].
DAVIDSON, AL ;
ARION, WJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1987, 253 (01) :156-167
[9]  
EXTON JH, 1981, ADV CYCL NUCL RES<D>, V14, P491
[10]   Effects of glucagon on glycogenolysis and gluconeogenesis ore region-specific in periportal and perivenous hepatocytes [J].
Ikezawa, Y ;
Yamatani, K ;
Ogawa, A ;
Ohnuma, H ;
Igarashi, M ;
Daimon, M ;
Manaka, H ;
Sasaki, H .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1998, 132 (06) :547-555