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首页> 外文期刊>Drug news & perspectives >G13-mediated signaling as a potential target for antiplatelet drugs.
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G13-mediated signaling as a potential target for antiplatelet drugs.

机译:G13介导的信号传导可能是抗血小板药物的潜在靶标。

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The activation of platelets at sites of vascular injury is essential for primary hemostasis, but also underlies arterial thrombosis leading to myocardial infarction or stroke. The inhibition of platelet function is therefore a major strategy to prevent and treat arterial thrombosis. Platelet stimuli like ADP, thrombin or thromboxane A(2) activate receptors that are coupled to heterotrimeric G proteins to regulate intracellular signaling pathways. Activation of platelets through these receptors has been shown to involve signaling through various heterotrimeric G proteins. The G protein G(13), which is able to link receptors to the Rho/Rho-kinase pathway, has recently been shown to be critically involved in platelet activation and to play an important role in platelet-dependent arterial thrombosis. The G(13)-mediated signaling pathway may therefore be an interesting new target for antiplatelet drugs.
机译:血管损伤部位的血小板活化对于原发性止血是必不可少的,但也是导致心肌梗塞或中风的动脉血栓形成的基础。因此,抑制血小板功能是预防和治疗动脉血栓形成的主要策略。像ADP,凝血酶或血栓烷A(2)这样的血小板刺激物会激活与异源三聚体G蛋白偶联的受体,从而调节细胞内信号通路。已经显示通过这些受体的血小板活化涉及通过各种异三聚体G蛋白的信号传导。 G蛋白G(13),能够将受体连接到Rho / Rho激酶途径,最近已被证明与血小板活化至关重要,并在依赖血小板的动脉血栓形成中起重要作用。因此,G(13)介导的信号通路可能是抗血小板药物有趣的新靶标。

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