Abstract
Nitric oxide (NO) and carbon monoxide (CO) are synthesized from l-arginine and heme by the catalytic reaction of NO synthase (NOS) and heme oxygenase (HO). NO, a highly reactive free radical, plays an important role in the regulation of vascular and immune function, antiapoptosis, and neurotransmission by producing cGMP, nitrosyl iron complexes, and S-nitrosothiols. CO, a more stable molecule, exerts similar biological activities to those of NO by cGMP production, p38 mitogen-activated protein kinase activation, and nuclear factor-κB activation. NO induces the suppression of apoptosis and inflammation in hepatocytes and macrophages by an elevation in HO-1 and CO production, and these effects were not observed in mice lacking HO-1 as well as in cells treated with a HO-1 inhibitor. These evidences indicate that the HO-1/CO pathway is a key player in NO-mediated cytoprotection and anti-inflammation. This chapter reviews new advances in the interactive relations between iNOS/NO and HO-1/CO pathways in the regulation of apoptosis and inflammation.
Original language | English |
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Title of host publication | Nitric Oxide, Part G Oxidative and Nitrosative Stress in Redox Regulation of Cell Signaling |
Publisher | Academic Press Inc. |
Pages | 329-338 |
Number of pages | 10 |
ISBN (Print) | 9780123743091 |
DOIs | |
Publication status | Published - 2008 |
Publication series
Name | Methods in Enzymology |
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Volume | 441 |
ISSN (Print) | 0076-6879 |
Bibliographical note
Funding Information:This work was supported by the Vascular System Research Center Grant from the Korea Science and Engineering Foundation.
All Science Journal Classification (ASJC) codes
- Biochemistry
- Molecular Biology