Corbic Milena, Sretenovic Jasmina, Zivkovic Vladimir, Jakovljevic Vladimir, Nikolic Turnic Tamara
Department of Neurology, Agnes Karll Laatzen Hospital, Laatzen, Germany.
Department of Physiology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.
Iran J Public Health. 2023 May;52(5):870-879. doi: 10.18502/ijph.v52i5.12704.
Three selective and most used inhibitors of PDE-5-sildenafil, vardenafil and tadalafil- have been successfully used for the treatment of erectile dysfunction. Erectile dysfunction and cardiovascular diseases might be considered as two dissimilar clinical signs of the identical systemic disease. PDE-5 inhibitors can through different models and mechanisms induce vasodilation, decrease apoptosis and cell proliferation, and they are widely present in various tissues that make them promising targets in a range of cardiovascular diseases.
PubMed was explored to identify papers published from 1990-2019, presenting data for the most used PDE-5 inhibitors (sildenafil, tadalafil or vardenafil) in treatment of cardiovascular diseases.
This article analyses the therapeutic potentials of PDE-5 inhibitors in cardiovascular diseases and discusses mechanisms, possible risks and limitations. Comparable to earlier studies, newer studies suggest cardioprotective effects of PDE-5 inhibitors, which include different models and mechanisms and do not indicate an increased rate of significant cardiovascular adverse reactions. Dissimilarity in the pharmacokinetics and pharmacodynamics of PDE-5 inhibitors are significant to their risk- benefit profile and clinical use. Some of the studies suggesting infarct size reduction after PDE-5 inhibition described the especially close dose-effect relation, other studies dosage adaptation in drug- drug interactions.
PDE-5 inhibitors indicate the encouraging useful effects by ischemia/reperfusion injury, myocar-dial infarction, cardiac hypertrophy, cardiomyopathy and systolic and diastolic congestive heart failure. Therefore, this and similar reviews can help for additional clinical targeting in the therapy of cardiovascular diseases.
三种选择性且最常用的磷酸二酯酶5(PDE - 5)抑制剂——西地那非、伐地那非和他达拉非——已成功用于治疗勃起功能障碍。勃起功能障碍和心血管疾病可能被视为同一全身性疾病的两种不同临床症状。PDE - 5抑制剂可通过不同模型和机制诱导血管舒张、减少细胞凋亡和细胞增殖,并且广泛存在于各种组织中,这使其成为一系列心血管疾病中颇具前景的靶点。
检索PubMed以识别1990年至2019年发表的论文,这些论文提供了关于最常用的PDE - 5抑制剂(西地那非、他达拉非或伐地那非)治疗心血管疾病的数据。
本文分析了PDE - 5抑制剂在心血管疾病中的治疗潜力,并讨论了其机制、可能的风险和局限性。与早期研究类似,最新研究表明PDE - 5抑制剂具有心脏保护作用,其作用包括不同的模型和机制,且未显示出严重心血管不良反应发生率增加。PDE - 5抑制剂在药代动力学和药效学方面的差异对其风险 - 效益概况和临床应用具有重要意义。一些研究表明PDE - 5抑制后梗死面积减小,描述了特别紧密的剂量 - 效应关系,其他研究则涉及药物相互作用中的剂量调整。
PDE - 5抑制剂在缺血/再灌注损伤、心肌梗死、心脏肥大、心肌病以及收缩性和舒张性充血性心力衰竭方面显示出令人鼓舞的有益效果。因此,本文及类似综述有助于为心血管疾病治疗提供更多临床靶点。