Dipeptidyl peptidase IV inhibition as an approach to the treatment and prevention of type 2 diabetes: a historical perspective

被引：44

作者：

Deacon, CF ^{[1
]}

Holst, JJ ^{[1
]}

机构：

[1] Univ Copenhagen, Panum Inst, Dept Med Physiol, DK-2200 Copenhagen N, Denmark

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 2002年 / 294卷 / 01期

关键词：

D O I：

10.1016/S0006-291X(02)00359-5

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：

[No abstract available]

引用

页码：1 / 4

页数：4

共 48 条

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[2]

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[5]

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[7]

Deacon C. F., 1996, REGUL PEPTIDES, V64, P30

[8] Degradation of endogenous and exogenous gastric inhibitory polypeptide in healthy and in type 2 diabetic subjects as revealed using a new assay for the intact peptide [J].

Deacon, CF ;

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[9] Dipeptidyl peptidase IV inhibition potentiates the insulinotropic effect of glucagon-like peptide 1 in the anesthetized pig [J].

Deacon, CF ;

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Holst, JJ .

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[10] Dipeptidyl peptidase IV inhibition reduces the degradation and clearance of GIP and potentiates its insulinotropic and antihyperglycemic effects in anesthetized pigs [J].

Deacon, CF ;

Danielson, P ;

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Holst, JJ .

DIABETES, 2001, 50 (07) :1588-1597

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