Sitagliptin therapy enhances the number of circulating angiogenic cells and angiogenesis-evaluations in vitro and in the rat critical limb ischemia model

Cytotherapy. 2013 Sep;15(9):1148-63. doi: 10.1016/j.jcyt.2013.05.005. Epub 2013 Jul 10.

Abstract

Background aims: We tested the hypothesis that sitagliptin is capable of increasing blood flow in the rat critical limb ischemia (CLI) model by enhancement of angiogenesis.

Methods: Adipose tissue from adult-male Fischer 344 rats (n = 6) were cultured in endothelial progenitor cell culture medium for 14 d with (25 μmol/L) or without sitagliptin. CLI was induced by ligation of the left femoral artery. Rats (n = 32) were equally separated into four groups: untreated controls (group 1), sitagliptin (4 mg/kg per day; group 2), CLI (group 3) and CLI with sitagliptin (group 4).

Results: In vitro, 7 and 14 d after cell culture, endothelial progenitor cell biomarkers assessed by flow cytometry (Sca-1/CD31+, CXCR4+, c-kit+ and CD34+ cells) and Western blot (vascular endothelial growth factor, CXCR4 and stromal-derived factor [SDF]-1α) were remarkably higher in group 4 than in the other groups (all P < 0.01). In vivo, 2 and 14 d after the CLI procedure, circulating angiogenic cell (Sca-1/CD31+, Sca-1+ and CD31+) numbers were significantly higher in group 4 than in the other groups (all P < 0.001). Additionally, the messenger RNA and protein expression of angiogenic biomarkers (CXCR4, SDF-1α and vascular endothelial growth factor), immunofluorescent staining of angiogenic cells (CXCR4+, SDF-1α+, CD31+, von Willebrand factor + cells) and immunohistochemical staining of small vessel numbers in the ischemic area were significantly higher in group 4 than in the other groups (all P < 0.01). Furthermore, laser Doppler showed that the ratio of ischemic/normal blood flow was remarkably higher group 4 than in group 3 by days 14 and 28 after the CLI procedure (all P < 0.01).

Conclusions: Sitagliptin therapy enhances circulating angiogenic cell numbers, angiogenesis and blood flow in the CLI area.

Keywords: angiogenesis; endothelial progenitor cells; laser Doppler blood flow; sitagliptin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism
  • Adipose Tissue / physiopathology
  • Animals
  • Arteries / drug effects
  • Arteries / metabolism
  • Arteries / physiology
  • Biomarkers / metabolism
  • Cell Movement / drug effects
  • Cell Movement / physiology
  • Disease Models, Animal
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Endothelial Cells / physiology
  • Hindlimb / drug effects*
  • Hindlimb / metabolism
  • Hindlimb / physiology
  • Ischemia / drug therapy*
  • Ischemia / metabolism
  • Ischemia / physiopathology
  • Male
  • Neovascularization, Physiologic / drug effects*
  • Neovascularization, Physiologic / physiology*
  • Pyrazines / pharmacology*
  • Rats
  • Rats, Inbred F344
  • Regional Blood Flow / drug effects
  • Regional Blood Flow / physiology
  • Sitagliptin Phosphate
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Stem Cells / physiology
  • Triazoles / pharmacology*

Substances

  • Biomarkers
  • Pyrazines
  • Triazoles
  • Sitagliptin Phosphate