Role of Insulin in Glucose-Stimulated Insulin Secretion in Beta Cells

被引:10
|
作者
Goren, H. Joseph [1 ]
机构
[1] Univ Calgary, Fac Med, Dept Biochem & Mol Biol, Calgary, AB, Canada
关键词
Insulin signaling; Islet glucose oxidation; Pyruvate dehydrogenase; Glucokinase; Anti-insulin inhibition of insulin secretion; beta cell communication; Constitutively secreted insulin;
D O I
10.2174/157339905774574301
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes is on the increase worldwide and greater than 90% are type 2. There are two features to type 2 diabetes: muscle, fat and liver tissues are insulin resistant and beta cells lose the ability to secrete insulin. Prior to developing diabetes, however, insulin resistant individuals lose the first-phase insulin secretion response. Transgenic mice lacking insulin receptors in their beta cells have no first-phase response. Primary cultures of mouse islets pre-exposed to anti-insulin do not exhibit a first-phase insulin secretion response. That is, beta cells, like muscle, fat, and liver, are an insulin sensitive tissue and in the presence of insulin resistance (type 2 diabetes), in the absence of insulin receptors (transgenic mice lacking b cell insulin receptors), or in the absence of constitutively secreted insulin (anti-insulin treatment), beta cells are unable to respond properly to post-prandial glucose. The purpose of this report is to review our understanding of the glucose-stimulus response and of insulin signaling, and to suggest why the latter may be necessary for the former to proceed.
引用
收藏
页码:309 / 330
页数:22
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