The biology of incretin hormones

被引:1748
作者
Drucker, DJ [1 ]
机构
[1] Univ Toronto, Toronto Gen Hosp, Banting & Best Diabet Ctr, Dept Med, Toronto, ON M5G 2C4, Canada
关键词
D O I
10.1016/j.cmet.2006.01.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gut peptides, exemplified by glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) are secreted in a nutrient-dependent manner and stimulate glucose-dependent insulin secretion. Both GIP and GLP-1 also promote beta cell proliferation and inhibit apoptosis, leading to expansion of beta cell mass. GLP-1, but not GIP, controls glycemia via additional actions on glucose sensors, inhibition of gastric emptying, food intake and glucagon secretion. Furthermore, GLP-1, unlike GIP, potently stimulates insulin secretion and reduces blood glucose in human subjects with type 2 diabetes. This article summarizes current concepts of incretin action and highlights the potential therapeutic utility of GLP-1 receptor agonists and dipepticlyl pepticlase-4 (DPP-4) inhibitors for the treatment of type 2 diabetes.
引用
收藏
页码:153 / 165
页数:13
相关论文
共 128 条
  • [51] DEGRADATION OF GLUCOSE-DEPENDENT INSULINOTROPIC POLYPEPTIDE AND TRUNCATED GLUCAGON-LIKE PEPTIDE-1 IN-VITRO AND IN-VIVO BY DIPEPTIDYL PEPTIDASE-IV
    KIEFFER, TJ
    MCINTOSH, CHS
    PEDERSON, RA
    [J]. ENDOCRINOLOGY, 1995, 136 (08) : 3585 - 3596
  • [52] Development and characterization of a glucagon-like peptide 1-albumin conjugate -: The ability to activate the glucagon-like peptide 1 receptor in vivo
    Kim, JG
    Baggio, LL
    Bridon, DP
    Castaigne, JP
    Robitaille, MF
    Jetté, L
    Benquet, C
    Drucker, DJ
    [J]. DIABETES, 2003, 52 (03) : 751 - 759
  • [53] Glucose-dependent insulinotropic polypeptide (GIP) stimulation of pancreatic β-cell survival is dependent upon phosphatidylinositol 3-kinase (PI3K)/protein kinase B (PKB) signaling, inactivation of the forkhead transcription factor Foxo1, and down-regulation of bax expression
    Kim, SJ
    Winter, K
    Nian, C
    Tsuneoka, M
    Koda, Y
    McIntosh, CHS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (23) : 22297 - 22307
  • [54] Islet transplantation outcomes in mice are better with fresh islets and exendin-4 treatment
    King, A
    Lock, J
    Xu, G
    Bonner-Weir, S
    Weir, GC
    [J]. DIABETOLOGIA, 2005, 48 (10) : 2074 - 2079
  • [55] Kinzig KP, 2002, J NEUROSCI, V22, P10470
  • [56] Brain glucagon-like peptide-1 increases insulin secretion and muscle insulin resistance to favor hepatic glycogen storage
    Knauf, C
    Cani, PD
    Perrin, C
    Iglesias, MA
    Maury, JF
    Bernard, E
    Benhamed, F
    Grémeaux, T
    Drucker, DJ
    Kahn, CR
    Girard, J
    Tanti, JF
    Delzenne, NM
    Postic, C
    Burcelin, R
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (12) : 3554 - 3563
  • [57] REDUCTION OF THE INCRETIN EFFECT IN RATS BY THE GLUCAGON-LIKE PEPTIDE-1 RECEPTOR ANTAGONIST EXENDIN(9-39) AMIDE
    KOLLIGS, F
    FEHMANN, HC
    GOKE, R
    GOKE, B
    [J]. DIABETES, 1995, 44 (01) : 16 - 19
  • [58] KREYMANN B, 1987, LANCET, V2, P1300
  • [59] CD26 (dipeptidyl-peptidase IV)-dependent recruitment of T cells in a rat asthma model
    Kruschinski, C
    Skripuletz, T
    Bedoui, S
    Tschernig, T
    Pabst, R
    Nassenstein, C
    Braun, A
    von Hörsten, S
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2005, 139 (01) : 17 - 24
  • [60] cAMP dose-dependently prevents palmitate-induced apoptosis by both protein kinase A- and cAMP-guanine nucleotide exchange factor-dependent pathways in β-cells
    Kwon, G
    Pappan, KL
    Marshall, CA
    Schaffer, JE
    McDaniel, ML
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (10) : 8938 - 8945