Metformin inhibits inflammatory angiogenesis in a murine sponge model

Biomed Pharmacother. 2010 Mar;64(3):220-5. doi: 10.1016/j.biopha.2009.08.004. Epub 2009 Oct 24.

Abstract

To investigate the effects of metformin on angiogenesis, on inflammatory cell accumulation and on production of endogenous cytokines in sponge implant in mice. Polyester-polyurethane sponges were implanted in Swiss mice and metformin (40 or 400mg/kg/day) was given orally for six days. The implants collected at day 7 postimplantation were processed for the assessment of hemoglobin (Hb), myeloperoxidase (MPO), N-acetylglucosaminidase (NAG) e collagen used as indexes for angiogenesis, neutrophil and macrophage accumulation and extracellular matrix deposition, respectively. Relevant inflammatory, angiogenic and fibrogenic cytokines were also determined. Metformin treatment attenuated the main components of the fibrovascular tissue, wet weight, vascularization (Hb content), macrophage recruitment (NAG activity), collagen deposition and the levels of transforming growth factor (TGF-beta1) intraimplant. A regulatory function of metformin on multiple parameters of main components of inflammatory angiogenesis has been revealed giving insight into the potential therapeutic underlying the actions of metformin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / pharmacology
  • Angiogenesis Inhibitors / therapeutic use*
  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use*
  • Chemokine CCL2 / biosynthesis
  • Chemokine CCL2 / genetics
  • Chemotaxis, Leukocyte / drug effects
  • Collagen / biosynthesis
  • Collagen / genetics
  • Drug Evaluation, Preclinical
  • Foreign-Body Reaction / drug therapy*
  • Foreign-Body Reaction / metabolism
  • Foreign-Body Reaction / physiopathology
  • Inflammation / physiopathology
  • Inflammation / prevention & control*
  • Male
  • Metformin / pharmacology
  • Metformin / therapeutic use*
  • Mice
  • Neovascularization, Pathologic / prevention & control*
  • Peroxidase / analysis
  • Surgical Sponges
  • Transforming Growth Factor beta1 / biosynthesis
  • Transforming Growth Factor beta1 / genetics
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / genetics
  • Vascular Endothelial Growth Factor A / biosynthesis
  • Vascular Endothelial Growth Factor A / genetics

Substances

  • Angiogenesis Inhibitors
  • Anti-Inflammatory Agents
  • Ccl2 protein, rat
  • Chemokine CCL2
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, rat
  • Collagen
  • Metformin
  • Peroxidase