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논문 기본 정보

자료유형
학술저널
저자정보
Yoo, Hayoung (College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University) Ku, Sae-Kwang (Department of Anatomy and Histology, College of Korean Medicine, Daegu Haany University) Lee, Wonhwa (College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University) Kwak, Soyoung (College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University) Baek, Young-Doo (Department of Clinical Pathology, Daegu Health College) Min, Byung-Woon (Department of BioMedical Clinical Pathology, Hanlyo University) Jeong, Gil-Saeng (College of Pharmacy, Keimyung University) Bae, Jong-Sup (College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제37권 제8호
발행연도
2014.1
수록면
1,069 - 1,078 (10page)

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Cudratricusxanthone A (CTXA), a natural bioactive compound extracted from the roots of Cudrania tricuspidata Bureau, is known to possess hepatoprotective, antiproliferative and anti-inflammatory activities. However, antiplatelet, anticoagulant, and profibrinolytic properties have not been studied. The anticoagulant activities of CTXA were measured by monitoring activated partial thromboplastin-time (aPTT), prothrombin time (PT), and the activities of cell-based thrombin and activated factor X (FXa). The effects of CTXA on the expressions of plasminogen activator inhibitor type 1 (PAI-1) and tissue-type plasminogen activator (t-PA) were also tested in tumor necrosis $factor-{\alpha}(TNF-{\alpha})$ activated human umbilical vein endothelial cells. Our data showed that CTXA inhibited thrombin-catalyzed fibrin polymerization and platelet aggregation, prolonged aPTT and PT significantly and inhibited the activities and production of thrombin and FXa. CTXA prolonged in vivo bleeding time and inhibited $TNF-{\alpha}$ induced PAI-1 production. Furthermore, PAI-1/t-PA ratio was significantly decreased by CTXA. Collectively, these results indicate that CTXA possesses antithrombotic activities and suggest that the current study could provide bases for the development of new anticoagulant agents.

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