Concentration dependence and time course of the effects of glucose on adenine and guanine nucleotides in mouse pancreatic islets

被引:115
作者
Detimary, P
VandenBerghe, G
Henquin, JC
机构
[1] UNIV CATHOLIQUE LOUVAIN,FAC MED,UNITE ENDOCRINOL & METAB,B-1200 BRUSSELS,BELGIUM
[2] UNIV CATHOLIQUE LOUVAIN,FAC MED,CHIM PHYSIOL LAB,B-1200 BRUSSELS,BELGIUM
关键词
D O I
10.1074/jbc.271.34.20559
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Changes in the ATP:ADP ratio in pancreatic B cells may participate in the regulation of insulin secretion by glucose. Here, we have investigated the possible role of guanine nucleotides. Mouse islets were incubated in a control medium (when K+-ATP channels are the major site of regulation) or in a high K+ medium (when glucose modulates the effectiveness of cytosolic Ca2+ on exocytosis). Glucose induced a concentration-dependent (0-20 mM) increase in GTP and a decrease in GDP in both types of medium, thus causing a progressive rise of the GTP:GDP ratio, ATP and ADP levels were 4-5-fold higher but varied in a similar way as those of guanine nucleotides. Insulin secretion was inversely correlated with ADP and GDP levels and positively correlated with the ATP:ADP and GTP:GDP ratios between 6 and 20 mM glucose in control medium and between 0 and 20 mM glucose in high K+ medium, The increases in the GTP:GDP and ATP:ADP ratios induced by a rise of glucose were faster than the decreases induced by a fall in glucose, but the changes of both ratios were again parallel. In conclusion, glucose causes large, concentration-dependent changes in guanine as well as in adenine nucleotides in islet cells. This raises the possibility that both participate in the regulation of nutrient-induced insulin secretion.
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页码:20559 / 20565
页数:7
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共 50 条
[1]   ENERGY REQUIREMENTS FOR INSULIN RELEASE FROM RAT PANCREAS IN-VITRO [J].
ALEYASSINE, H .
ENDOCRINOLOGY, 1970, 87 (01) :84-+
[2]   ELECTROPHYSIOLOGY OF THE PANCREATIC BETA-CELL [J].
ASHCROFT, FM ;
RORSMAN, P .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1989, 54 (02) :87-143
[3]  
ASHCROFT FM, 1992, INSULIN MOL BIOL PAT, P97
[4]   INTERRELATIONSHIP OF ISLET METABOLISM, ADENOSINE-TRIPHOSPHATE CONTENT AND INSULIN RELEASE [J].
ASHCROFT, SJ ;
WEERASINGHE, LC ;
RANDLE, PJ .
BIOCHEMICAL JOURNAL, 1973, 132 (02) :223-231
[5]   SEPARATE PROCESSES MEDIATE NUCLEOTIDE-INDUCED INHIBITION AND STIMULATION OF THE ATP-REGULATED K+-CHANNELS IN MOUSE PANCREATIC BETA-CELLS [J].
BOKVIST, K ;
AMMALA, C ;
ASHCROFT, FM ;
BERGGREN, PO ;
LARSSON, O ;
RORSMAN, P .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1991, 243 (1307) :139-144
[6]   INTRACELLULAR ATP DIRECTLY BLOCKS K+ CHANNELS IN PANCREATIC B-CELLS [J].
COOK, DL ;
HALES, CN .
NATURE, 1984, 311 (5983) :271-273
[7]   2 SITES OF GLUCOSE CENTRAL OF INSULIN RELEASE WITH DISTINCT DEPENDENCE ON THE ENERGY-STATE IN PANCREATIC B-CELLS [J].
DETIMARY, P ;
GILON, P ;
NENQUIN, M ;
HENQUIN, JC .
BIOCHEMICAL JOURNAL, 1994, 297 :455-461
[8]   POSSIBLE LINKS BETWEEN GLUCOSE-INDUCED CHANGES IN THE ENERGY-STATE OF PANCREATIC B-CELLS AND INSULIN RELEASE - UNMASKING BY DECREASING A STABLE POOL OF ADENINE-NUCLEOTIDES IN MOUSE ISLETS [J].
DETIMARY, P ;
JONAS, JC ;
HENQUIN, JC .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (04) :1738-1745
[9]   GALANIN ACTIVATES NUCLEOTIDE-DEPENDENT K+ CHANNELS IN INSULIN-SECRETING CELLS VIA A PERTUSSIS TOXIN-SENSITIVE G-PROTEIN [J].
DUNNE, MJ ;
BULLETT, MJ ;
LI, GD ;
WOLLHEIM, CB ;
PETERSEN, OH .
EMBO JOURNAL, 1989, 8 (02) :413-420
[10]   POTASSIUM SELECTIVE ION CHANNELS IN INSULIN-SECRETING CELLS - PHYSIOLOGY, PHARMACOLOGY AND THEIR ROLE IN STIMULUS-SECRETION COUPLING [J].
DUNNE, MJ ;
PETERSEN, OH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1071 (01) :67-82