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Modulation of platelet membrane function via exogenous lipid moiety exposure alters platelet responsiveness to shear

机译:通过外源性脂质部分暴露的血小板膜功能的调节改变了血小板反应剪切

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Shear-induced platelet activation may cause life-threatening thrombosis, particularly in patients with mechanical support devices or coronary atherosclerosis. The majority of present anti-platelet agents target or interfere with biochemical, rather than physical mechanisms of platelet activation. Less data and understanding exists with regard to pharmacologic modulation of shear-mediated platelet activation. In this work, we hypothesized that modulating cell membrane properties, via alteration of membrane composition through addition of exogenous lipid moieties, would alter platelet responsiveness to shear. Here we tested fatty acids, lecithin and cholesterol as additive lipid compounds. We demonstrated that incorporation of fatty acids (DHA/EPA) or lecithin into the platelet membrane triggered enhanced sensitivity of platelets to shear-mediated activation. On the other hand, cholesterol incorporation provides significant protection, limiting the effect of shear on platelet activation. These findings provide valuable insight for the development of therapeutic strategies that can modulate shear-mediated platelet activation.
机译:剪切诱导的血小板活化可能导致危及生命的血栓形成,特别是在机械支撑装置或冠状动脉粥样硬化的患者中。大多数本发明的抗血小板药物靶向或干扰生化,而不是血小板活化的物理机制。关于剪切介导的血小板活化的药理学调节较少的数据和理解。在这项工作中,我们假设通过加入外源性脂质部分通过膜组合物改变调节细胞膜性能,将改变血小板反应性以剪切。在这里,我们测试了脂肪酸,卵磷脂和胆固醇作为添加剂脂质化合物。我们证明,将脂肪酸(DHA / EPA)或卵磷脂掺入血小板膜中触发的血小板敏感性,以剪切介导的活化。另一方面,胆固醇的合并提供了显着的保护,限制了剪切对血小板活化的影响。这些发现提供了有价值的洞察力,可以调节剪切介导的血小板激活的治疗策略。

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