Divakaran Sanjay, Loscalzo Joseph
Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
J Am Coll Cardiol. 2017 Nov 7;70(19):2393-2410. doi: 10.1016/j.jacc.2017.09.1064.
The use of nitroglycerin in the treatment of angina pectoris began not long after its original synthesis in 1847. Since then, the discovery of nitric oxide as a biological effector and better understanding of its roles in vasodilation, cell permeability, platelet function, inflammation, and other vascular processes have advanced our knowledge of the hemodynamic (mostly mediated through vasodilation of capacitance and conductance arteries) and nonhemodynamic effects of organic nitrate therapy, via both nitric oxide-dependent and -independent mechanisms. Nitrates are rapidly absorbed from mucous membranes, the gastrointestinal tract, and the skin; thus, nitroglycerin is available in a number of preparations for delivery via several routes: oral tablets, sublingual tablets, buccal tablets, sublingual spray, transdermal ointment, and transdermal patch, as well as intravenous formulations. Organic nitrates are commonly used in the treatment of cardiovascular disease, but clinical data limit their use mostly to the treatment of angina. They are also used in the treatment of subsets of patients with heart failure and pulmonary hypertension. One major limitation of the use of nitrates is the development of tolerance. Although several agents have been studied for use in the prevention of nitrate tolerance, none are currently recommended owing to a paucity of supportive clinical data. Only 1 method of preventing nitrate tolerance remains widely accepted: the use of a dosing strategy that provides an interval of no or low nitrate exposure during each 24-h period. Nitric oxide's important role in several cardiovascular disease mechanisms continues to drive research toward finding novel ways to affect both endogenous and exogenous sources of this key molecular mediator.
1847年硝酸甘油最初合成后不久,便开始用于治疗心绞痛。从那时起,一氧化氮作为一种生物效应物的发现以及对其在血管舒张、细胞通透性、血小板功能、炎症和其他血管过程中作用的更深入了解,通过一氧化氮依赖性和非依赖性机制,推进了我们对有机硝酸盐治疗的血流动力学(主要通过容量血管和传导血管的舒张介导)和非血流动力学效应的认识。硝酸盐可从粘膜、胃肠道和皮肤迅速吸收;因此,硝酸甘油有多种制剂可供通过多种途径给药:口服片剂、舌下片剂、颊含片、舌下喷雾剂、透皮软膏、透皮贴剂以及静脉制剂。有机硝酸盐常用于治疗心血管疾病,但临床数据将其使用主要局限于心绞痛的治疗。它们也用于治疗部分心力衰竭和肺动脉高压患者。使用硝酸盐的一个主要限制是耐受性的产生。尽管已经研究了几种药物用于预防硝酸盐耐受性,但由于缺乏支持性临床数据,目前尚无推荐药物。目前唯一广泛接受的预防硝酸盐耐受性的方法是采用一种给药策略,即在每24小时期间提供一个无硝酸盐或低硝酸盐暴露的间隔期。一氧化氮在几种心血管疾病机制中的重要作用继续推动着寻找影响这种关键分子介质内源性和外源性来源新方法的研究。