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      The inhibitory effect of tachyplesin I on thrombosis and its mechanisms.

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          Abstract

          Thrombotic diseases are major cause of cardiovascular diseases. This study was designed to investigate the effect of tachyplesin I on platelet aggregation and thrombosis. Platelet aggregation was analysed with a whole blood aggregometer. The mice were employed to investigate the effect of tachyplesin I on thrombosis in vivo. Tachyplesin I inhibited thrombin-induced platelet aggregation in a dose-dependent manner. Furthermore, tachyplesin I significantly reduced thrombosis in carrageenan-induced tail thrombosis model by intraperitoneal injection (0.1, 0.2 or 0.4 mg/kg) or intragastric administration (15, 30 or 60 mg/kg). Tachyplesin I also prolonged the bleeding time (BT) and clotting time (CT). The results revealed that tachyplesin I inhibited platelet aggregation and thrombosis by interfering the PI3K/AKT pathway. Tachyplesin I did not show significantly toxicity to mice under 300 mg/kg via intravenous injection. The results show that tachyplesin I inhibits thrombosis and has low toxicity. It is suggested that tachyplesin I has the potential to develop a new anti-thrombotic drug.

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          Author and article information

          Journal
          Chem Biol Drug Des
          Chemical biology & drug design
          Wiley
          1747-0285
          1747-0277
          September 2019
          : 94
          : 3
          Affiliations
          [1 ] Department of Biochemistry and Molecular Biology, Guangdong Medical University, Zhanjiang, China.
          [2 ] Guangdong Key Laboratory for Research and Development of Natural Drugs, Guangdong Medical University, Zhanjiang, China.
          [3 ] Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China.
          Article
          10.1111/cbdd.13570
          31108023
          87b9c123-40dc-4490-9b61-f6a9432032d8
          © 2019 John Wiley & Sons A/S.
          History

          PI3K/Akt,anti-thrombosis,platelet aggregation,tachyplesin I

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