Hinokitiol is a novel glycoprotein VI antagonist on human platelets

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题名:	Hinokitiol is a novel glycoprotein VI antagonist on human platelets
作者:	Wan-Jung Lu;Ming-Ping Wu;Kuan-Hung Lin;Yu-Chen Lin;Hsiu-Chu Chou;Joen-Rong Sheu
贡献者:	視光學系
关键词:	Collagen receptors;convulxin;glycoprotein VI;hinokitiol;platelet activation
日期:	2014-01-01
上传时间:	2025-08-01 15:07:02 (UTC+8)
摘要:	Hinokitiol (4-isopropyl-tropolone) is a bioactive compound with various pharmacological activities that is found in the wood of cupressaceous plants. Platelet activation plays an important role in thrombogenesis. In our previous study, hinokitiol specifically inhibited collagen-induced platelet aggregation ex vivo and prolonged thrombogenesis in vivo. The glycoprotein (GP) VI and integrin α2?1 are major collagen receptors that mediate platelet adhesion and aggregation. In our current study, we investigated which of these collagen receptors is involved in the hinokitiol-mediated inhibition of platelet activation. Treatment with 2?100?µM hinokitiol caused a dose-dependent right, parallel shift in the collagen concentration?response curve (0.5?10?µg/ml), with no change in the maximal responses. Furthermore, hinokitiol inhibited platelet aggregation and relative [Ca2+]i mobilization stimulated by convulxin, an agonist of GP VI, but not by aggretin, an agonist of integrin α2?1, indicating that hinokitiol mediates the inhibition of platelet activation through GP VI, rather than through integrin α2?1. Hinokitiol also specifically inhibited the convulxin-mediated activation of protein kinase C, phospholipase C?2, Akt, mitogen-activated protein kinases, and Lyn. Hinokitiol markedly diminished the co-immunoprecipitation of GP VI-bound Lyn after convulxin stimulation. In conclusion, hinokitiol, an antagonist of collagen GP VI may represent a novel antiplatelet drug for the prevention of thrombi associated with coronary and cerebral artery diseases.
關聯:	Platelets, 25(8), 595-602. https://doi.org/10.3109/09537104.2013.863856
显示于类别:	[視光學系] 期刊論文

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