Tranilast inhibits the proliferation, chemotaxis and tube formation of human microvascular endothelial cells in vitro and angiogenesis in vivo

Abstract

1. First developed as an antiallergic drug, tranilast inhibits chemical mediator release from mast cells. In the present study, we examine the effects of tranilast on angiogenesis in vitro and in vivo and discuss the application of tranilast for angiogenic diseases.

2. Tranilast inhibited significantly the proliferation (IC₅₀: 136 μM, 95% confidence limits: 124–137 μM) and vascular endothelium growth factor (VEGF)-induced chemotaxis (IC₅₀: 135 μM, 95% confidence limits: 124–147 μM) of human dermal microvascular endothelial cells (HDMECs) at concentrations greater than 25 μg ml⁻¹. No toxicity to HDMECs measuring by LDH release and no inhibitory effects on metalloproteinase (MMP)-2 and MMP-9 activity were observed even at 100 μg ml⁻¹ (306 μM).

3. Tube formation of HDMECs cultured on the matrigel as an in vitro angiogenesis model was inhibited by tranilast in a concentration-dependent manner. The IC₅₀ value and 95% confidence limits were 175 μM and 151–204 μM, respectively.

4. In vivo angiogenesis was induced in mice by the subcutaneous injection of matrigel containing 30 ng ml⁻¹ VEGF and 64 μg ml⁻¹ heparin. Tranilast was administered orally twice a day for 3 days. Tranilast dose-dependently suppressed angiogenesis in the matrigel and a significant change was observed at a dose of 300 mg kg⁻¹.

5. These results indicate that tranilast is an angiogenesis inhibitor which may be beneficial for the improvement of angiogenic diseases such as proliferative diabetic retinopathy, age-related macular degeneration, tumour invasion and rheumatoid arthritis.

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