首页> 外文期刊>Cardiovascular & Hematological Agents in Medicinal Chemistry (Formerly Current Medicinal Chemistry - Cardiovascular & Hematological Agents) >Inflammation in Cardiovascular Disease and Regulation of the Actin Cytoskeleton in Inflammatory Cells: The Actin Cytoskeleton as a Target
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Inflammation in Cardiovascular Disease and Regulation of the Actin Cytoskeleton in Inflammatory Cells: The Actin Cytoskeleton as a Target

机译:心血管疾病中的炎症和炎性细胞中肌动蛋白细胞骨架的调控:以肌动蛋白细胞骨架为靶标

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摘要

Cardiovascular disease is prevalent in developed countries causing very large burdens to health services. The underlying pathology is atheromatous plaque in the sub-endothelial region of the vascular wall. High levels of low density lipoprotein cholesterol and high blood pressure cause endothelial damage. Atheroma develop from a response to this injury that is perpetuated to chronic inflammation. The invasion of inflammatory leukocytes into atheroma during its development and in the precipitation of acute thrombotic events is mediated by adhesion molecules on the cell surface. These are regulated by the actin filament cytoskeleton which also mediates intracellular signalling from them. The actin cytoskeleton is central to NADPH oxidase activation that produces superoxide which is an intracellular signalling molecule for the hypertensive and inflammatory actions of angiotensin II. There are polymorphisms in actin filament proteins such as adducin and caldesmon and in the promoter regions of tropomyosins that may cause individual variation in these processes. Many signalling molecules in the actin filament response to inflammatory stimuli and in signalling downstream from actin filaments are small G-proteins that require post-transcriptional modification by isoprenoids from the cholesterol synthetic pathway. Statins deplete the isoprenoids and so down regulate G-proteins that mediate the inflammatory response. Angiotensin converting enzyme inhibitors and angiotensin II receptor type 1 antagonists decrease angiotensin II stimulated superoxide production thus decreasing not only blood pressure but also inflammation. The antiinflammatory effects of these drugs, involving altered actin filament function, are a major contributor to their benefits in the treatment of cardiovascular disease. The feasibility of modifying the behaviour of actin filament proteins as a therapeutic approach for cardiovascular disease is considered.
机译:心血管疾病在发达国家很普遍,给医疗服务造成了很大负担。潜在的病理是血管壁内皮下区域的动脉粥样斑块。高水平的低密度脂蛋白胆固醇和高血压会引起内皮损伤。动脉粥样硬化是由对这种伤害的反应发展而来的,这种反应长期伴随着慢性炎症。炎性白细胞在其发展过程中以及在急性血栓形成事件的沉淀过程中侵入动脉粥样硬化是由细胞表面的粘附分子介导的。这些受肌动蛋白丝细胞骨架的调节,肌动蛋白丝细胞骨架也介导它们的细胞内信号传导。肌动蛋白的细胞骨架是NADPH氧化酶激活的中心,NADPH氧化酶激活产生超氧化物,超氧化物是用于血管紧张素II的高血压和炎性作用的细胞内信号分子。肌动蛋白丝蛋白(例如,adducin和caldesmon)以及原肌球蛋白的启动子区域存在多态性,可能导致这些过程中的个体差异。肌动蛋白丝中的许多信号分子对炎症刺激以及肌动蛋白丝下游的信号均是小的G蛋白,需要通过胆固醇合成途径中的类异戊二烯进行转录后修饰。他汀类药物会消耗类异戊二烯,因此会下调介导炎症反应的G蛋白。血管紧张素转换酶抑制剂和血管紧张素II受体1型拮抗剂可降低血管紧张素II刺激的超氧化物生成,从而不仅降低血压,而且降低炎症。这些药物的抗炎作用涉及肌动蛋白丝功能的改变,是其在治疗心血管疾病中的主要作用。考虑了改变肌动蛋白丝蛋白的行为作为治疗心血管疾病的可行性。

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