Temporal profiles and clinical significance of pulsatile insulin secretion

被引:35
作者
Polonsky, KS [1 ]
Sturis, J [1 ]
Van Cauter, E [1 ]
机构
[1] Univ Chicago, Dept Med, Pritzker Sch Med, Chicago, IL 60637 USA
关键词
insulin secretion; pulses; NIDDM; C-peptide; ultradian oscillations;
D O I
10.1159/000023168
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this article, recent experiments are reviewed which have addressed the role of oscillatory insulin secretion in the pathophysiology of glucose intolerance and diabetes. The ultradian oscillations of insulin secretion appear to be an integral part of the feedback loop between glucose and insulin secretion and as a result are abnormal in states of glucose intolerance. Treatment of impaired glucose tolerance with troglitazone, a thiazolidinedione that improves insulin sensitivity, leads to an improvement in the ability of the beta-cell to sense and respond to a glucose stimulus restoring the ability of glucose to entrain the ultradian oscillations. The rapid oscillations of insulin secretion appear to be an inherent feature of the cellular mechanisms of insulin secretion since they persist in the isolated perfused pancreas and in perifused islets. These oscillations are paralleled by changes in intracellular Ca2+ and are also abnormal in states of glucose intolerance and diabetes. Available evidence indicates that these alterations are due to decreased expression of voltage-dependent Ca2+ channels on the beta-cell membrane.
引用
收藏
页码:178 / 184
页数:7
相关论文
共 20 条
[1]   Elevated plasma glucose 2 h postchallenge predicts defects in beta-cell function [J].
Byrne, MM ;
Sturis, J ;
Sobel, RJ ;
Polonsky, KS .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1996, 270 (04) :E572-E579
[2]   Treatment with the oral antidiabetic agent troglitazone improves beta cell responses to glucose in subjects with impaired glucose tolerance [J].
Cavaghan, MK ;
Ehrmann, DA ;
Byrne, MM ;
Polonsky, KS .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (03) :530-537
[3]   IMPACT OF INTENSIVE VENOUS SAMPLING ON CHARACTERIZATION OF PULSATILE GH RELEASE [J].
EVANS, WS ;
FARIA, ACS ;
CHRISTIANSEN, E ;
HO, KY ;
WEISS, J ;
ROGOL, AD ;
JOHNSON, ML ;
BLIZZARD, RM ;
VELDHUIS, JD ;
THORNER, MO .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (04) :E549-E556
[4]   RAPID FLUCTUATIONS IN PLASMA-CATECHOLAMINES IN MONKEYS UNDER UNDISTURBED CONDITIONS [J].
HANSEN, BC ;
SCHIELKE, GP ;
JEN, KLC ;
WOLFE, RA ;
MOVAHED, H ;
PEK, SB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 242 (01) :E40-E46
[5]  
LAND DA, 1979, NEW ENGL J MED, V301, P1023
[6]  
MATTHEWS DR, 1983, DIABETOLOGIA, V24, P231
[7]   LACK OF CONTROL BY GLUCOSE OF ULTRADIAN INSULIN SECRETORY OSCILLATIONS IN IMPAIRED GLUCOSE-TOLERANCE AND IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
OMEARA, NM ;
STURIS, J ;
VANCAUTER, E ;
POLONSKY, KS .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :262-271
[8]   24-HOUR PROFILES AND PULSATILE PATTERNS OF INSULIN-SECRETION IN NORMAL AND OBESE SUBJECTS [J].
POLONSKY, KS ;
GIVEN, BD ;
VANCAUTER, E .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (02) :442-448
[9]   IGF-I inhibits burst mass of pulsatile insulin secretion at supraphysiological and low IGF-I infusion rates [J].
Porksen, N ;
Hussain, MA ;
Bianda, TL ;
Nyholm, B ;
Christiansen, JS ;
Butler, PC ;
Veldhuis, JD ;
Froesch, ER ;
Schmitz, O .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 272 (03) :E352-E358
[10]   Mechanisms of sulfonylurea's stimulation of insulin secretion in vivo - Selective amplification of insulin secretory burst mass [J].
Porksen, NK ;
Munn, SR ;
Steers, JL ;
Schmitz, O ;
Veldhuis, JD ;
Butler, PC .
DIABETES, 1996, 45 (12) :1792-1797