Dipeptidyl peptidase-4 inhibitors

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GLP-1 and DPP-4 inhibitors
GLP-1 and DPP-4 inhibitors

Inhibitors of Dipeptidyl peptidase 4 , also DPP-4 inhibitors, are a new class of oral hypoglycemics which block DPP-4.

Their mechanism of action is thought to result from increased Incretin levels (GLP-1 and GIP),[1][2][3] which, inhibit glucagon release (which increases the blood glucose) but more importantly increase insulin secretion and decrease gastric emptying.

Drugs belonging to this class are vildagliptin[4], sitagliptin[5], saxagliptin and alogliptin.

Although extensive long-term, pre-clinical studies of the major DPP-4 inhibitors has failed to show any evidence of potential to cause tumors in laboratory animals, there was one in-vitro (i.e., test tube) study that has raised some questions. [6]

Sitagliptin entered the Australian drug market in late 2007 for the treatment of difficult to control diabetes mellitus type 2.

[edit] References

  1. ^ McIntosh CH, Demuth HU, Pospisilik JA, Pederson R. Dipeptidyl peptidase IV inhibitors: how do they work as new antidiabetic agents? Regul Pept. 2005 Jun 15;128(2):159-65. PMID:15780435 [1].
  2. ^ Behme MT, Dupre J, McDonald TJ. Glucagon-like peptide 1 improved glycemic control in type 1 diabetes. BMC Endocr Disord. 2003 Apr 10;3(1):3. PMID 12697069. Full Free Text.
  3. ^ Dupre J, Behme MT, Hramiak IM, McFarlane P, Williamson MP, Zabel P, McDonald TJ. Glucagon-like peptide I reduces postprandial glycemic excursions in IDDM. Diabetes. 1995 Jun;44(6):626-30. PMID 7789625.
  4. ^ Banting and Best Diabetes Centre at UT laf237 - Vildagliptin
  5. ^ Banting and Best Diabetes Centre at UT mk-0431 - Sitagliptin
  6. ^ Masur K et al. DPPIV inhibitors extend GLP-2 mediated tumour promoting effects on intestinal cancer cells, Regul Pept. ,137 (3) p. 147-55 (2006) PMID 16908079.

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