摘要
心血管疾病(CVD)与调节血管壁收缩状态和细胞组成的内皮功能障碍有关。最近的大量临床试验表明,脂质修饰干预措施降低了高胆固醇血症患者和低密度脂蛋白胆固醇水平相对正常者的CVD风险。他们还强调了脂质不依赖的明确降脂药物 - 他汀类药物的作用,抑制3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶,并用于治疗高胆固醇血症和减少动脉粥样硬化。他汀类的新型治疗方法包括它们对血红素加氧酶1(HO-1)和HO-1相关信号通路如激活蛋白(AP)-1,蛋白激酶G(PKG),细胞外基质调节激酶(ERK), p38 MAPK或NFκB在血管壁细胞中的表达。该综述旨在描述在最常见的CVD中不同他汀类药物诱导HO-1的分子机制。
关键词: 腹主动脉瘤,抗氧化剂,动脉粥样硬化,心脏病,心血管疾病,血红素加氧酶-1,氧化应激,他汀类药物。
图形摘要
Current Drug Targets
Title:The Role of Statins in the Activation of Heme Oxygenase-1 in Cardiovascular Diseases
Volume: 18 Issue: 6
关键词: 腹主动脉瘤,抗氧化剂,动脉粥样硬化,心脏病,心血管疾病,血红素加氧酶-1,氧化应激,他汀类药物。
摘要: Cardiovascular diseases (CVD) are associated with the dysfunction of endothelium that regulates the contractile state of vascular walls and cellular composition. Recent large clinical trials indicated that lipid-modifying interventions decrease the risk of CVD in patients with hypercholesterolemia and in those with relatively normal levels of LDL cholesterol. They also highlighted lipid-independent role of well-established lipid-lowering drugs- statins- which inhibit 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and are used in the treatment of hypercholesterolemia and reduction of atherosclerosis. Novel therapeutic approaches of statins include their influence on heme oxygenase 1 (HO-1) and HO-1 related signaling pathways such as activator protein (AP)-1, protein kinase G (PKG), extracellular matrix-regulated kinase (ERK), p38 MAPK or NFκB in vascular wall cells. This review aimed to describe the molecular mechanisms involved in the induction of HO-1 under different statins in the most common CVD.
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The Role of Statins in the Activation of Heme Oxygenase-1 in Cardiovascular Diseases, Current Drug Targets 2017; 18 (6) . https://dx.doi.org/10.2174/1389450117666160401123600
DOI https://dx.doi.org/10.2174/1389450117666160401123600 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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