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Importance of timing of antiaggregant treatment in the prevention of radiation induced enteropathy.

机译:抗凝治疗时机在预防放射性诱发肠病中的重要性。

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Chronic radiation enteropathy (CRE) is an undesirable radiation-induced toxicity and a common health problem in patients with pelvic or abdominal malignancies. Damage to microvascular endothelial cells and connective tissue is blamed to cause this adverse effect. It is shown that platelets are the first cellular elements that initiate the homeostatic and inflammatory responses and release of several proinflammatory and fibrinogenic mediators. Antiplatelet agents such as ticlopidine and clopidogrel were shown to prevent CRE and this effect is believed to be directed by their activities against thrombocytes. However, recent studies have shown that these drugs also induce apoptosis in endothelial cells and may lead to decreased expression of endothelial prostacyclin and thrombomodulin (TM) and increased release of von Willebrand factor which are shown to be major contributors of coagulation process. Assuming that radiation induced apoptosis occur 6-10h after irradiation, we think that timing of these antiaggregant drugs with irradiation is important and a 6-10h interval between these may be beneficial to avoid this adverse interaction.
机译:慢性放射性肠病(CRE)是骨盆或腹部恶性肿瘤患者不良的辐射诱发毒性和常见的健康问题。责怪对微血管内皮细胞和结缔组织的损害会引起这种不利影响。结果表明,血小板是引发稳态和炎性反应并释放几种促炎性和纤维蛋白原性介质的首批细胞因子。已显示抗血小板药物如噻氯匹定和氯吡格雷可预防CRE,据信这种作用是由其对血小板的活性所决定的。但是,最近的研究表明,这些药物还可以诱导内皮细胞凋亡,并可能导致内皮前列环素和血栓调节蛋白(TM)的表达降低以及von Willebrand因子的释放增加,这被认为是凝血过程的主要贡献者。假设辐射诱导的细胞凋亡发生在辐射后6-10h,我们认为这些抗凝集药物的辐射时机很重要,并且它们之间的6-10h间隔对于避免这种不良相互作用可能是有益的。

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