SLOW AND FAST OSCILLATIONS OF CYTOPLASMIC CA2+ IN PANCREATIC-ISLETS CORRESPOND TO PULSATILE INSULIN RELEASE

被引:104
作者
BERGSTEN, P
机构
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1995年 / 268卷 / 02期
关键词
INSULIN TRANSIENTS; CYTOPLASMIC CALCIUM CONCENTRATION; ISLETS OF LANGERHANS; ENDOCRINE PANCREAS;
D O I
10.1152/ajpendo.1995.268.2.E282
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytoplasmic Ca2+ concentration ([Ca2+](i)) and insulin secretion were monitored in single ob/ob mouse pancreatic islets stimulated by glucose. After culture in 5.5 mM of the sugar, islets responded to 11 mM glucose with pulsatile insulin secretion synchronized with oscillations of [Ca2+](i) (0.3-0.5/min). Most islets also showed superimposed regular rapid [Ca2+](i) oscillations and insulin transients of similar frequency. Whereas the amplitude of the slow insulin pulses increased in 20 mM glucose, the [Ca2+](i) oscillations were replaced by a sustained increase. After culture in the absence of sugar, there was little rise of [Ca2+](i) during exposure to 11 mM glucose and only a slight secretory response, which, however, was pulsatile. The slow secretory pulses in the presence of 11 mM glucose were augmented after culture in 11 or 20 mM glucose despite a sustained elevation of [Ca2+](i). Although pulsatile insulin release was not always associated with [Ca2+](i) oscillations, the data indicate that the slow and fast [Ca2+](i) oscillations do correspond to pulsatile insulin secretion.
引用
收藏
页码:E282 / E287
页数:6
相关论文
共 29 条
[1]   INSULIN FROM INDIVIDUAL ISOLATED ISLETS OF LANGERHANS .1. RESPONSE TO GLUCOSE [J].
BEIGELMAN, PM ;
THOMAS, LJ ;
SLAVIN, B ;
SHU, MJ ;
BESSMAN, SP .
BIOCHEMICAL MEDICINE, 1973, 8 (03) :392-402
[2]   GLUCOSE-INDUCED AMPLITUDE REGULATION OF PULSATILE INSULIN-SECRETION FROM INDIVIDUAL PANCREATIC-ISLETS [J].
BERGSTEN, P ;
HELLMAN, B .
DIABETES, 1993, 42 (05) :670-674
[3]   GLUCOSE-INDUCED CYCLES OF INSULIN RELEASE CAN BE RESOLVED INTO DISTINCT PERIODS OF SECRETORY ACTIVITY [J].
BERGSTEN, P ;
HELLMAN, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 192 (03) :1182-1188
[4]  
BERGSTEN P, 1994, J BIOL CHEM, V269, P8749
[5]   GLUCOSE INHIBITS INSULIN RELEASE WHEN NOT PROMOTING THE ENTRY OF CALCIUM INTO THE BETA-CELLS [J].
BERGSTEN, P ;
HELLMAN, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 125 (03) :875-881
[6]  
GILON P, 1992, J BIOL CHEM, V267, P20713
[7]   INSULIN, GLUCAGON, AND GLUCOSE EXHIBIT SYNCHRONOUS, SUSTAINED OSCILLATIONS IN FASTING MONKEYS [J].
GOODNER, CJ ;
WALIKE, BC ;
KOERKER, DJ ;
ENSINCK, JW ;
BROWN, AC ;
CHIDECKEL, EW ;
PALMER, J ;
KALNASY, L .
SCIENCE, 1977, 195 (4274) :177-179
[8]   RAPID REDUCTION AND RETURN OF SURFACE INSULIN-RECEPTORS AFTER EXPOSURE TO BRIEF PULSES OF INSULIN IN PERIFUSED RAT HEPATOCYTES [J].
GOODNER, CJ ;
SWEET, IR ;
HARRISON, HC .
DIABETES, 1988, 37 (10) :1316-1323
[9]   GLUCOSE-INDUCED OSCILLATIONS OF CYTOPLASMIC CA-2+ IN THE PANCREATIC BETA-CELL [J].
GRAPENGIESSER, E ;
GYLFE, E ;
HELLMAN, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 151 (03) :1299-1304
[10]   3 TYPES OF CYTOPLASMIC CA-2+ OSCILLATIONS IN STIMULATED PANCREATIC BETA-CELLS [J].
GRAPENGIESSER, E ;
GYLFE, E ;
HELLMAN, B .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1989, 268 (01) :404-407