Chung Hun-Taeg, Pae Hyun-Ock, Cha Young-Nam
Department of Microbiology and Immunology, Wonkwang University School of Medicine, Iksan, Chonbuk 570-749, Republic of Korea.
Curr Pharm Des. 2008;14(5):422-8. doi: 10.2174/138161208783597335.
Great attention has been placed on the protective role of heme oxygenase-1 (HO-1) for several vascular diseases such as atherosclerosis. HO-1, by exerting anti-inflammatory, antiproliferative, anti-apoptotic and anti-oxidant effects on the vasculature, protects against atherosclerosis. The precise underlying mechanisms for HO-1-based protection are not yet completely understood, but appear to involve the protective effects of HO-1 by-products, carbon monoxide (CO), biliverdin/bilirubin and free iron. Among the HO-1 by-products, CO has been shown to mimic some protective actions of HO-1, specifically, in vascular system. There is evidence supporting that HO-1-derived CO also interacts with other gaseous molecules, such as nitric oxide (NO) and hydrogen sulfide (H2S) that may relate to either vascular protection or injury. CO, NO and H2S not only exert comparable biological actions but also compete with and are antagonists with each other for maintaining vascular homeostasis. This review will highlight the protective roles of HO-1/CO in vascular injury/disease, and emphasize the potential roles of CO in possible interplay among three gaseous molecules, which may be important to explore the overall protective roles of HO-1/CO system in the pathogenesis of human vascular disease.
血红素加氧酶-1(HO-1)对动脉粥样硬化等多种血管疾病的保护作用已受到高度关注。HO-1通过对血管系统发挥抗炎、抗增殖、抗凋亡和抗氧化作用,从而预防动脉粥样硬化。基于HO-1的保护的确切潜在机制尚未完全明确,但似乎涉及HO-1的副产物一氧化碳(CO)、胆绿素/胆红素和游离铁的保护作用。在HO-1的副产物中,CO已被证明可模拟HO-1的一些保护作用,特别是在血管系统中。有证据支持HO-1衍生的CO还与其他气体分子相互作用,如一氧化氮(NO)和硫化氢(H2S),它们可能与血管保护或损伤有关。CO、NO和H2S不仅发挥类似的生物学作用,而且相互竞争并相互拮抗以维持血管稳态。本综述将重点阐述HO-1/CO在血管损伤/疾病中的保护作用,并强调CO在三种气体分子可能的相互作用中的潜在作用,这对于探索HO-1/CO系统在人类血管疾病发病机制中的整体保护作用可能具有重要意义。