Hyperinsulinism of infancy:: towards an understanding of unregulated insulin release

被引:32
作者
Shepherd, RM
Cosgrove, KE
O'Brien, RE
Barnes, PD
Ämmälä, C
Dunne, MJ
机构
[1] Univ Sheffield, Inst Mol Physiol, Sheffield S10 2TN, S Yorkshire, England
[2] Univ Sheffield, Dept Biomed Sci, Sheffield S10 2TN, S Yorkshire, England
来源
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION | 2000年 / 82卷 / 02期
关键词
hypoglycaemia; ATP sensitive potassium channels; insulin secretion; nesidioblastosis; hyperinsulinism; diazoxide;
D O I
10.1136/fn.82.2.F87
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Insulin is synthesised, stored, and secreted from pancreatic beta cells. These are located within the islets of Langerhans, which are distributed throughout the pancreas. Less than 2% of the total pancreas is devoted to an endocrine function. When the mechanisms that control insulin release are compromised, potentially lethal diseases such as diabetes and neonatal hypoglycaemia are manifest. This article reviews the physiology of insulin release and illustrates how defects in these processes will result in the pathophysiology of hyperinsulinism of infancy.
引用
收藏
页码:F87 / F97
页数:11
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