Literature DB >> 18177233

Redox-based therapeutics for lung diseases.

Yuma Hoshino1, Michiaki Mishima.   

Abstract

Because oxidative stress is such a common factor of lung diseases, we cannot help asking why so many diseases are caused by the same oxidative stress. It is likely to be a consequence of diversity in sources and location of oxidative stress, and concomitant factors. The aim of this forum is to characterize the disease-specific involvement of oxidative stress and to make use of it for therapeutics. It is also of note that oxidative-stress biomarkers are useful tools for disease management. Exhaled nitric oxide has been established as a marker of bronchial asthma in clinical practice. By using recent noninvasive techniques, such as exhaled breath condensate, other markers of lipid peroxidation or antioxidants are now under evaluation. Antioxidant therapy, as represented by N-acetylcysteine, has widely been tested as a treatment for lung disorders, but it has had limited success in clinical practice. The clinical outcome might be improved by combination therapy or better patient selection. Novel antioxidant drugs are also under investigation. Molecular targeted therapy against redox-sensitive signaling pathways could be an alternative therapeutic approach. Moreover, disease-specific pathways have been identified whose regulation could be more efficient and less toxic than regulating universal pathways.

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Year:  2008        PMID: 18177233     DOI: 10.1089/ars.2007.1961

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  15 in total

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Review 2.  Effects of bioactive compounds from Pleurotus mushrooms on COVID-19 risk factors associated with the cardiovascular system.

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Review 3.  Aryl Hydrocarbon Receptor in Oxidative Stress as a Double Agent and Its Biological and Therapeutic Significance.

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Review 4.  Superoxide dismutase mimics: chemistry, pharmacology, and therapeutic potential.

Authors:  Ines Batinić-Haberle; Júlio S Rebouças; Ivan Spasojević
Journal:  Antioxid Redox Signal       Date:  2010-09-15       Impact factor: 8.401

5.  N-acetylcysteine inhibits alveolar epithelial-mesenchymal transition.

Authors:  V M Felton; Z Borok; B C Willis
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2009-07-31       Impact factor: 5.464

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7.  The extracellular redox state modulates mitochondrial function, gluconeogenesis, and glycogen synthesis in murine hepatocytes.

Authors:  Laura Nocito; Amber S Kleckner; Elsia J Yoo; Albert R Jones Iv; Marc Liesa; Barbara E Corkey
Journal:  PLoS One       Date:  2015-03-27       Impact factor: 3.240

8.  Free radicals, antioxidants in disease and health.

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Journal:  Int J Biomed Sci       Date:  2008-06

9.  HIV-1 transgene expression in rats causes oxidant stress and alveolar epithelial barrier dysfunction.

Authors:  Coy Lassiter; Xian Fan; Pratibha C Joshi; Barbara A Jacob; Roy L Sutliff; Dean P Jones; Michael Koval; David M Guidot
Journal:  AIDS Res Ther       Date:  2009-02-04       Impact factor: 2.250

10.  The functional role of MnSOD as a biomarker of human diseases and therapeutic potential of a new isoform of a human recombinant MnSOD.

Authors:  Antonella Borrelli; Antonietta Schiattarella; Patrizia Bonelli; Franca Maria Tuccillo; Franco Maria Buonaguro; Aldo Mancini
Journal:  Biomed Res Int       Date:  2014-01-06       Impact factor: 3.411

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