Role of heme oxygenase-1 in vascular disease

被引:59
作者
Chung, Hun-Taeg [1 ]
Pae, Hyun-Ock [1 ,2 ]
Cha, Young-Nam [3 ]
机构
[1] Wonkwang Univ Sch Med, Dept Microbiol & Immunol, Iksan 570749, Chonbuk, South Korea
[2] Wonkwang Univ, Grad Sch Oriental Med, Iksan 570749, Chonbuk, South Korea
[3] Inha Univ, Coll Med, Dept Pharmacol & Toxicol, Inchon 400712, South Korea
关键词
heme oxygense-1; vascular disease; carbon monoxide; nitric oxide; hydrogen sulfide;
D O I
10.2174/138161208783597335
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
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 byproducts, 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.
引用
收藏
页码:422 / 428
页数:7
相关论文
共 93 条
[1]
Abe K, 1996, J NEUROSCI, V16, P1066
[2]
Stem cell therapy for vascular disease [J].
Adams, Benjamin ;
Xiao, Qingzhong ;
Xu, Qingbo .
TRENDS IN CARDIOVASCULAR MEDICINE, 2007, 17 (07) :246-251
[3]
Transcriptional regulation of the heme oxygenase-1 gene via the stress response element pathway [J].
Alam, J ;
Cook, JL .
CURRENT PHARMACEUTICAL DESIGN, 2003, 9 (30) :2499-2511
[4]
Induction of heme oxygenase 1 by moderately oxidized low-density lipoproteins in human vascular smooth muscle cells: Role of mitogen-activated protein kinases and Nrf2 [J].
Anwar, AA ;
Li, FYL ;
Leake, DS ;
Ishii, T ;
Mann, GE ;
Siow, RCM .
FREE RADICAL BIOLOGY AND MEDICINE, 2005, 39 (02) :227-236
[5]
Heme, heme oxygenase and ferritin in vascular endothelial cell injury [J].
Balla, J ;
Vercellotti, GM ;
Jeney, V ;
Yachie, A ;
Varga, Z ;
Eaton, JW ;
Balla, G .
MOLECULAR NUTRITION & FOOD RESEARCH, 2005, 49 (11) :1030-1043
[6]
Curcurnin activates the haem oxygenase-1 gene via regulation of Nrf2 and the antioxidant-responsive element [J].
Balogun, E ;
Hoque, M ;
Gong, PF ;
Killeen, E ;
Green, CJ ;
Foresti, R ;
Alam, J ;
Motterlini, R .
BIOCHEMICAL JOURNAL, 2003, 371 :887-895
[7]
Structure of cerebral arterioles in cystathionine β-synthase-deficient mice [J].
Baumbach, GL ;
Sigmund, CD ;
Bottiglieri, T ;
Lentz, SR .
CIRCULATION RESEARCH, 2002, 91 (10) :931-937
[8]
Is hypertension an inflammatory process? [J].
Boos, Christopher J. ;
Lip, Gregory Y. H. .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (13) :1623-1635
[9]
NITRIC-OXIDE, A NOVEL NEURONAL MESSENGER [J].
BREDT, DS ;
SNYDER, SH .
NEURON, 1992, 8 (01) :3-11
[10]
Carbon monoxide generated by heme oxygenase 1 suppresses endothelial cell apoptosis [J].
Brouard, S ;
Otterbein, LE ;
Anrather, J ;
Tobiasch, E ;
Bach, FH ;
Choi, AMK ;
Soares, MP .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (07) :1015-1025