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Recent developments in the effects of nitric oxide-donating statins on cardiovascular disease through regulation of tetrahydrobiopterin and nitric oxide

机译:一氧化氮他汀类药物通过调节四氢生物蝶呤和一氧化氮对心血管疾病的作用的最新进展

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Since the discovery of the importance of nitric oxide (NO) to the human body three decades ago, numerous laboratory and clinical studies have been done to explore its potential therapeutic actions on many organs. In the cardiovascular system, NO works as a volatile signaling molecule regulating the vascular permeability and vascular tone, preventing thrombosis and inflammation, as well as inhibiting the smooth muscle hyperplasia. Thus, NO is important in the prevention and treatment of cardiovascular disease. NO is synthesized by NO synthase (NOS) with tetrahydrobiopterin (BH4) as the crucial cofactor. Many studies have been done to form nitric oxide donors so as to deliver NO directly to the vessel walls. In addition, NO moieties have been incorporated into existing therapeutic agents to enhance the NO bioavailability, including statins. Statins are inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme (HMG-CoA), the rate-limiting enzyme of the mevalonate pathway. By inhibiting this pathway, statins lower blood cholesterol and exert their pleiotropic effects through activity in reaction cascades, such as Rho/ROCK and Rac 1/NADPH oxidase pathways. Statins have also been observed to implement their non-lipid effects by promoting BH4 synthesis with increase of NO bioavailability. Furthermore, NO-donating statins in laboratory studies have demonstrated to produce better therapeutic effects than their parent's drugs. They offer better anti-inflammatory, anti-proliferative and antithrombotic actions on cardiovascular system. They also cause better revascularization in peripheral ischemia and produce greater enhancement in limb reperfusion and salvage. In addition, it has been shown that NO-donating statin caused less myotoxicity, the most common side effect related to treatment with statins. The initial studies have demonstrated the superior therapeutic effects of NO-donating statins while producing fewer side effects. Crown Copyright (C) 2014 Published by Elsevier Inc. All rights reserved.
机译:自三年前发现一氧化氮(NO)对人体的重要性以来,已经进行了许多实验室和临床研究,以探索其对许多器官的潜在治疗作用。在心血管系统中,NO用作调节血管通透性和血管张力的挥发性信号分子,可防止血栓形成和炎症以及抑制平滑肌增生。因此,NO对于预防和治疗心血管疾病很重要。 NO是由NO合酶(NOS)以四氢生物蝶呤(BH4)作为关键辅因子合成的。已经进行了许多研究以形成一氧化氮供体,以便将NO直接递送至血管壁。另外,已经将NO部分掺入现有的治疗剂中以增强NO的生物利用度,包括他汀类。他汀类药物是3-羟-3-甲基戊二酰辅酶(HMG-CoA)的抑制剂,HMG-CoA是甲羟戊酸途径的限速酶。通过抑制该途径,他汀类药物可降低血液中的胆固醇水平,并通过反应级联反应(例如Rho / ROCK和Rac 1 / NADPH氧化酶途径)发挥其多效作用。还观察到他汀类药物通过促进BH4合成并增加NO生物利用度来实现其非脂质作用。此外,实验室研究中的NO捐赠他汀类药物已证明比其母体药物产生更好的治疗效果。它们对心血管系统具有更好的抗炎,抗增殖和抗血栓作用。它们还会在周围缺血中引起更好的血运重建,并在肢体再灌注和抢救中产生更大的增强作用。另外,已经表明,捐赠NO的他汀引起的肌毒性较小,这是与他汀治疗有关的最常见的副作用。最初的研究表明,捐赠NO的他汀类药物具有更好的治疗效果,同时产生的副作用更少。 Crown版权所有(C)2014,Elsevier Inc.保留所有权利。

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