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The relevance of epigenetics to occlusive cerebral and peripheral arterial disease

机译:表观生物学与闭塞性脑和外周动脉疾病的相关性

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Athero-thrombosis of the arteries supplying the brain and lower limb are the main causes of stroke and limb loss. New therapies are needed to improve the outcomes of athero-thrombosis. Recent evidence suggests a role for epigenetic changes in the development and progression of ischaemic injury due to atherosclerotic occlusion of peripheral arteries. DNA hypermethylation have been associated with cardiovascular diseases. Histone post-translational modifications have also been implicated in atherosclerosis. Oxidized low-density lipoprotein regulated pro-inflammatory gene expression within endothelial cells is controlled by phosphorylation/ acetylation of histone H3 and acetylation of histone H4 for example. There are a number of challenges in translating the growing evidence implicating epigenetics in atherosclerosis to improved therapies for patients. These include the small therapeutic window in conditions such as acute stroke and critical limb ischaemia, since interventions introduced in such patients need to act rapidly and be safe in elderly patients with many co-morbidities. Pre-clinical animal experiments have also reported conflicting effects of some novel epigenetic drugs, which suggest that further in-depth studies are required to better understand their efficacy in resolving ischaemic injury. Effective ways of dealing with these challenges are needed before epigenetic approaches to therapy can be introduced into practice.
机译:供给大脑和下肢的动脉的运动血栓形成是中风和肢体损失的主要原因。需要新的疗法来改善运动血栓形成的结果。最近的证据表明,由于外周动脉的动脉粥样硬化闭塞,对缺血性损伤的发展和进展的表现变化的作用。 DNA高甲基化已与心血管疾病有关。组蛋白的翻译后修饰也涉及动脉粥样硬化。内皮细胞内氧化的低密度脂蛋白调节的促炎基因表达是通过组蛋白H3的磷酸化/乙酰化和组蛋白H4的乙酰化控制。在翻译越来越多的证据暗指动脉粥样硬化中以改善患者的疗法,存在许多挑战。这些包括在诸如急性卒中和临界肢体缺血的条件下的小型治疗窗,因为在这些患者中引入的干预措施需要迅速行动,并且在老年人患有许多共同病态的老年患者中是安全的。临床前的动物实验还报告了一些新型表观遗传药物的矛盾影响,这表明需要进一步深入研究,以更好地了解在解决缺血性损伤方面的疗效。在治疗的表观遗传方法之前需要处理处理这些挑战的有效方法。

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