Abstract
It is becoming increasingly apparent that reactive oxygen species (ROS), including superoxide anion and nitric oxide (NO), exert multiple biological effects over a wide spectrum, from physiological regulatory functions to damaging alterations contributing to the pathogenesis of diverse diseases. This chapter presents an overview of recent progress in the clinical application of oxidative stress biomarkers in pediatric medicine. First, the review briefly presents important physiological and pathophysiological aspects of ROS and antioxidative defense systems. Second, the interrelationship of NO system blockade, endothelial dysfunction, and oxidative stress is discussed. Third, a list of clinically applicable biomarkers is presented, along with pediatric diseases in which enhanced oxidative stress might be involved. Many good biomarkers are readily measurable using enzyme-linked immunosorbent assay. Rapid diagnostic tests for measuring oxidative stress status have been introduced. Fourth, age-related reference normal ranges of oxidative stress biomarkers are presented, including those for urinary acrolein-lysine, 8-hydroxy-2′-deoxyguanosine, nitrite/nitrate, and pentosidine. Finally, recent clinical studies that have evaluated the efficacy of antioxidative intervention for oxidative stress-related diseases are explained. Although not comprehensive, this review provides a brief perspective of current pediatric research which highlights the adverse health effects of ROS actions and therapeutic strategies for ROS-associated diseases.
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Abbreviations
- AD:
-
Atopic dermatitis
- ADMA:
-
Asymmetric dimethylarginine
- AG:
-
Aminoguanidine
- ASL:
-
Argininosuccinate lyase
- ASS:
-
Argininosuccinate synthase
- BAP:
-
Biological antioxidative potential
- BOM:
-
Bilirubin oxidative metabolites
- CAAT:
-
Cationic amino acid transporter
- CAT:
-
Catalase
- CML:
-
Carboxymethyllysine
- CO:
-
Carbon monoxide
- Cr:
-
Creatinine
- CSF:
-
Cerebrospinal fluid
- DDAH:
-
Dimethylarginine dimethylaminohydrolase
- ELISA:
-
Enzyme-linked immunosorbent assay
- GPX:
-
Glutathione peroxidase
- GSH:
-
Glutathione
- HNE:
-
4-Hydroxy-2-nonenal
- H2O2 :
-
Hydrogen peroxide
- l-NAME:
-
NG-nitro-l-arginine methyl ester
- LO:
-
Lipid alkoxyl radical
- LOO:
-
Lipid peroxyl radical
- LOOH:
-
Lipid hydroperoxide
- MDA:
-
Malondialdehyde
- NO:
-
Nitric oxide
- NO2 :
-
Nitrogen dioxide
- NOS:
-
Nitric oxide synthase
- 1O2 :
-
Singlet oxygen
- O2 − :
-
Superoxide anion
- OH:
-
Hydroxyl radical
- 8-OHdG:
-
8-Hydroxy-2′-deoxyguanosine
- ONOO:
-
Peroxynitrite radical
- ONOO− :
-
Peroxynitrite anion
- PRMT:
-
Protein arginine methyltransferase
- ROS:
-
Reactive oxygen species
- SOD:
-
Superoxide dismutase
- TBARS:
-
Thiobarbituric acid reactive substances
- TP:
-
Total hydroperoxides
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Acknowledgments
I thank Professor Tsuneo Morishima (Okayama University, Japan), Professor Mitsufumi Mayumi (University of Fukui), Professor Michael S. Goligorsky (New York Medical College, USA), and Professor Takanobu Ishida (State University of New York at Stony Brook, USA) for invaluable help with these studies. This work was supported by the Japanese Ministry of Health, Labour and Welfare.
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Tsukahara, H. (2014). Oxidative Stress Biomarkers: Current Status and Future Perspective. In: Tsukahara, H., Kaneko, K. (eds) Studies on Pediatric Disorders. Oxidative Stress in Applied Basic Research and Clinical Practice. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-0679-6_6
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