Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, Missouri 65212, USA.
Curr Drug Targets. 2010 Dec;11(12):1504-16. doi: 10.2174/1389450111009011504.
Heme oxygenase-1 (HO-1) metabolizes heme to generate carbon monoxide (CO), biliverdin, and iron. Biliverdin is subsequently metabolized to bilirubin by biliverdin reductase. HO-1 has recently emerged as a promising therapeutic target in the treatment of vascular disease. Pharmacological induction or gene transfer of HO-1 ameliorates vascular dysfunction in animal models of atherosclerosis, post-angioplasty restenosis, vein graft stenosis, thrombosis, myocardial infarction, and hypertension, while inhibition of HO-1 activity or gene deletion exacerbates these disorders. The vasoprotection afforded by HO-1 is largely attributable to its end products: CO and the bile pigments, biliverdin and bilirubin. These end products exert potent anti-inflammatory, antioxidant, anti-apoptotic, and anti-thrombotic actions. In addition, CO and bile pigments act to preserve vascular homeostasis at sites of arterial injury by influencing the proliferation, migration, and adhesion of vascular smooth muscle cells, endothelial cells, endothelial progenitor cells, or leukocytes. Several strategies are currently being developed to target HO-1 in vascular disease. Pharmacological induction of HO-1 by heme derivatives, dietary antioxidants, or currently available drugs, is a promising near-term approach, while HO-1 gene delivery is a long-term therapeutic goal. Direct administration of CO via inhalation or through the use of CO-releasing molecules and/or CO-sensitizing agents provides an attractive alternative approach in targeting HO-1. Furthermore, delivery of bile pigments, either alone or in combination with CO, presents another avenue for protecting against vascular disease. Since HO-1 and its products are potentially toxic, a major challenge will be to devise clinically effective therapeutic modalities that target HO-1 without causing any adverse effects.
血红素加氧酶-1(HO-1)将血红素代谢生成一氧化碳(CO)、胆红素和铁。胆红素随后被胆红素还原酶代谢生成胆红素。HO-1 最近成为治疗血管疾病的有前途的治疗靶点。HO-1 的药理学诱导或基因转移可改善动脉粥样硬化、血管成形术后再狭窄、静脉移植物狭窄、血栓形成、心肌梗死和高血压动物模型中的血管功能障碍,而 HO-1 活性的抑制或基因缺失会加重这些疾病。HO-1 提供的血管保护主要归因于其终产物:CO 和胆色素,胆红素和胆红素。这些终产物具有强大的抗炎、抗氧化、抗凋亡和抗血栓作用。此外,CO 和胆色素通过影响血管平滑肌细胞、内皮细胞、内皮祖细胞或白细胞的增殖、迁移和黏附,在动脉损伤部位发挥维持血管内稳态的作用。目前正在开发几种针对血管疾病中 HO-1 的策略。血红素衍生物、膳食抗氧化剂或现有药物对 HO-1 的药理学诱导是一种很有前途的近期方法,而 HO-1 基因转移是一种长期的治疗目标。通过吸入或使用 CO 释放分子和/或 CO 敏化剂直接给予 CO 提供了一种有吸引力的替代方法来靶向 HO-1。此外,单独或与 CO 联合递送胆色素也为预防血管疾病提供了另一种途径。由于 HO-1 和其产物具有潜在毒性,因此设计出一种针对 HO-1 的临床有效的治疗方式而不会引起任何不良反应将是一个主要挑战。