TY - JOUR T1 - Evaluation of Antithrombotic Activities of Solanum xanthocarpum and Tinospora cordifolia JF - Pharmacognosy Research Y1 - 2018 A1 - Onila Lugun A1 - Sobharani Bhoi A1 - Priyanka Kujur A1 - D. Vinay Kumar A1 - William R. Surin KW - Collagen KW - Platelet KW - Solanum xanthocarpum KW - Thrombin KW - Thrombosis KW - Tinospora cordifolia AB -

Background: Solanum xanthocarpum and Tinospora cordifolia have been reported to exhibit anti‑inflammatory, antiarthritic, antioxidant, antiallergic, and hepatoprotective activities. The origins of many of the currently available antithrombotic treatments are from natural products and natural sources. Objective: To investigate the antithrombotic activities of methanolic leaf extracts of S. xanthocarpum (SXME) and T. cordifolia (TCME). Materials and Methods: Antithrombotic activities were assessed by thrombin inhibition assay, thrombin generation assay, platelet adhesion assay on collagen‑coated surface, and platelet PAC1‑FITC binding by flow cytometry. Results: SXME significantly inhibited thrombin activity at 5–20 mg/ml concentrations, whereas TCME inhibited thrombin activity at 500 µg/ml–5 mg/ml concentrations. Further, SXME inhibited thrombin generation at 2–20 mg/ml concentrations, whereas TCME exhibited significant inhibition at 200 µg/ml, suggesting that TCME has higher efficacy as compared to SXME. Moreover, SXME did not inhibit platelet adhesion on collagen‑coated surface, whereas TCME inhibited platelet adhesion on collagen‑coated surface at 5 mg/ml. Indomethacin showed significant inhibition in platelet adhesion at 300 µM. Further, SXME inhibited thrombin‑induced platelet activation (PAC1‑FITC binding) significantly at 1 mg/ml by about 80%, whereas TCME inhibited thrombin‑induced platelet activation (PAC1‑FITC binding) by about 40% at 1 mg/ml. Conclusion: These results strongly suggested that SXME and TCME possess antithrombotic activities. However, further studies are essential to find out the active constituent responsible for antithrombotic effect.

VL - 10 IS - 1 ER -