Heme Oxygenase-1/Carbon Monoxide: Novel Therapeutic Strategies in Critical Care Medicine

Author(s): Stefan W. Ryter, Augustine M.K. Choi.

Journal Name: Current Drug Targets

Volume 11 , Issue 12 , 2010

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Abstract:

Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) remain major causes of morbidity and mortality in critical care medicine despite advances in therapeutic modalities. ALI can be associated with sepsis, trauma, pharmaceutical or xenobiotic exposures, high oxygen therapy (hyperoxia) and mechanical ventilation. The stress protein heme oxygenase-1 (HO-1) provides an inducible defense mechanism that can protect lung cells and tissues against injury. HO-1 degrades heme to biliverdin-IXα, carbon monoxide (CO), and iron. Each of these reaction products has been implicated in the cytoprotection associated with HO-1 expression. At low concentrations, CO can confer cyto-protective and tissue-protective effects involving the inhibition of inflammatory, proliferative, and apoptotic signaling. Lung protection by HO-1 has been demonstrated in vitro and in vivo in several models of experimental ALI and sepsis. Recent studies have also explored the protective effects of pharmacological or inhalation CO therapy in animal models of ALI/sepsis. CO has shown therapeutic potential in models of oxidative and acid-induced lung injury, ventilator-induced lung injury, endotoxin challenge, and cecal-ligation and puncture induced-sepsis. Despite therapeutic benefit in animal model studies, the efficacy of CO in humans with these conditions remains unclear, and awaits further controlled clinical studies. This review will summarize recent findings on the therapeutic applications of HO-1 and its end-product CO in the lung, with an emphasis on lung injury models relevant to critical care medicine.

Keywords: Carbon Monoxide, Heme Oxygenase-1, Inflammation, Lung Disease, Sepsis, Ventilator-Induced Lung Injury, acute respiratory, distress syndrome (ARDS), xenobiotic exposures, hyperoxia, cecal-ligation, lung injury (ALI), anti-inflammatory, anti-proliferative, antiapoptotic effects, molecular oxygen (O2), cytochrome p450 reductase, Coreleasing molecules (CORMs), lipopolysaccharide, stress response elements (StRE), hypoxia-inducible factor (Hif-1), heat shock factor-1, nuclear factor kappa-B (NF-κ;B), Zn-protoporphyrin-IX, neutrophil influx, ventilator-induced lung injury (VILI), smooth muscle cells (SMC), phagocytosis, bronchioalveolar lavage (BAL), mitogen activated protein kinase (MAPK), protein-1β, peroxisome proliferator activated receptor-γ (PPAR-γ), aortic smooth muscle, polymorphonuclear cells, spinal anesthesia, carbon monoxide releasing compounds (CORMs), neutrophil adhesion, Pseudomonas aeruginosa, alveolar-capillary, chronic obstructive pulmonary disease (COPD), Parts per million

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Article Details

VOLUME: 11
ISSUE: 12
Year: 2010
Page: [1485 - 1494]
Pages: 10
DOI: 10.2174/1389450111009011485
Price: $58

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